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<front>
<journal-meta>
<journal-id journal-id-type="pmc">CMC</journal-id>
<journal-id journal-id-type="nlm-ta">CMC</journal-id>
<journal-id journal-id-type="publisher-id">CMC</journal-id>
<journal-title-group>
<journal-title>Computers, Materials &#x0026; Continua</journal-title>
</journal-title-group>
<issn pub-type="epub">1546-2226</issn>
<issn pub-type="ppub">1546-2218</issn>
<publisher>
<publisher-name>Tech Science Press</publisher-name>
<publisher-loc>USA</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">63407</article-id>
<article-id pub-id-type="doi">10.32604/cmc.2025.063407</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Review</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Generative Artificial Intelligence (GAI) in Breast Cancer Diagnosis and Treatment: A Systematic Review</article-title>
<alt-title alt-title-type="left-running-head">Generative Artificial Intelligence (GAI) in Breast Cancer Diagnosis and Treatment: A Systematic Review</alt-title>
<alt-title alt-title-type="right-running-head">Generative Artificial Intelligence (GAI) in Breast Cancer Diagnosis and Treatment: A Systematic Review</alt-title>
</title-group>
<contrib-group>
<contrib id="author-1" contrib-type="author" corresp="yes">
<name name-style="western"><surname>Tan</surname><given-names>Xiao Jian</given-names></name><xref ref-type="aff" rid="aff-1">1</xref><xref ref-type="aff" rid="aff-2">2</xref><xref ref-type="aff" rid="aff-3">3</xref><xref rid="cor1" ref-type="corresp">&#x002A;</xref><email>tanxj@tarc.edu.my</email></contrib>
<contrib id="author-2" contrib-type="author">
<name name-style="western"><surname>Cheor</surname><given-names>Wai Loon</given-names></name><xref ref-type="aff" rid="aff-2">2</xref></contrib>
<contrib id="author-3" contrib-type="author">
<name name-style="western"><surname>Cheng</surname><given-names>Ee Meng</given-names></name><xref ref-type="aff" rid="aff-4">4</xref><xref ref-type="aff" rid="aff-5">5</xref></contrib>
<contrib id="author-4" contrib-type="author">
<name name-style="western"><surname>Lim</surname><given-names>Chee Chin</given-names></name><xref ref-type="aff" rid="aff-3">3</xref><xref ref-type="aff" rid="aff-4">4</xref></contrib>
<contrib id="author-5" contrib-type="author">
<name name-style="western"><surname>Rahman</surname><given-names>Khairul Shakir Ab</given-names></name><xref ref-type="aff" rid="aff-6">6</xref></contrib>
<aff id="aff-1"><label>1</label><institution>Biomedical and Bioinformatics Engineering (BBE) Research Group, Centre for Multimodal Signal Processing (CMSP), Tunku Abdul Rahman University of Management and Technology (TAR UMT)</institution>, <addr-line>Jalan Genting Kelang, Setapak, Kuala Lumpur, 53300</addr-line>, <country>Malaysia</country></aff>
<aff id="aff-2"><label>2</label><institution>Department of Electrical and Electronics Engineering, Faculty of Engineering and Technology, Tunku Abdul Rahman University of Management and Technology (TAR UMT)</institution>, <addr-line>Jalan Genting Kelang, Setapak, Kuala Lumpur, 53300</addr-line>, <country>Malaysia</country></aff>
<aff id="aff-3"><label>3</label><institution>Sports Engineering Research Centre (SERC), Universiti Malaysia Perlis (UniMAP)</institution>, <addr-line>Kampus Pauh Putra, Arau, 02600</addr-line>, <country>Perlis, Malaysia</country></aff>
<aff id="aff-4"><label>4</label><institution>Faculty of Electronic Engineering and Technology, Universiti Malaysia Perlis (UniMAP)</institution>, <addr-line>Kampus Pauh Putra, Arau, 02600</addr-line>, <country>Perlis, Malaysia</country></aff>
<aff id="aff-5"><label>5</label><institution>Advanced Communication Engineering (ACE) Centre of Excellence, Universiti Malaysia Perlis (UniMAP)</institution>, <addr-line>Kangar, 02600</addr-line>, <country>Malaysia</country></aff>
<aff id="aff-6"><label>6</label><institution>Department of Pathology, Hospital Tuanku Fauziah</institution>, <addr-line>Jalan Tun Abdul Razak, Kangar, 01000</addr-line>, <country>Malaysia</country></aff>
</contrib-group>
<author-notes>
<corresp id="cor1"><label>&#x002A;</label>Corresponding Author: Xiao Jian Tan. Email: <email>tanxj@tarc.edu.my</email></corresp>
</author-notes>
<pub-date date-type="collection" publication-format="electronic">
<year>2025</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>03</day><month>07</month><year>2025</year>
</pub-date>
<volume>84</volume>
<issue>2</issue>
<fpage>2015</fpage>
<lpage>2060</lpage>
<history>
<date date-type="received">
<day>14</day>
<month>1</month>
<year>2025</year>
</date>
<date date-type="accepted">
<day>15</day>
<month>5</month>
<year>2025</year>
</date>
</history>
<permissions>
<copyright-statement>&#x00A9; 2025 The Authors.</copyright-statement>
<copyright-year>2025</copyright-year>
<copyright-holder>Published by Tech Science Press.</copyright-holder>
<license xlink:href="https://creativecommons.org/licenses/by/4.0/">
<license-p>This work is licensed under a <ext-link ext-link-type="uri" xlink:type="simple" xlink:href="https://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution 4.0 International License</ext-link>, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
</license>
</permissions>
<self-uri content-type="pdf" xlink:href="TSP_CMC_63407.pdf"></self-uri>
<abstract>
<p>This study systematically reviews the applications of generative artificial intelligence (GAI) in breast cancer research, focusing on its role in diagnosis and therapeutic development. While GAI has gained significant attention across various domains, its utility in breast cancer research has yet to be comprehensively reviewed. This study aims to fill that gap by synthesizing existing research into a unified document. A comprehensive search was conducted following Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines, resulting in the retrieval of 3827 articles, of which 31 were deemed eligible for analysis. The included studies were categorized based on key criteria, such as application types, geographical distribution, contributing organizations, leading journals, publishers, and temporal trends. Keyword co-occurrence mapping and subject profiling further highlighted the major research themes in this field. The findings reveal that GAI models have been applied to improve breast cancer diagnosis, treatment planning, and outcome predictions. Geographical and network analyses showed that most contributions come from a few leading institutions, with limited global collaboration. The review also identifies key challenges in implementing GAI in clinical practice, such as data availability, ethical concerns, and model validation. Despite these challenges, the study highlights GAI&#x2019;s potential to enhance breast cancer research, particularly in generating synthetic data, improving diagnostic accuracy, and personalizing treatment approaches. This review serves as a valuable resource for researchers and stakeholders, providing insights into current research trends, major contributors, and collaborative networks in GAI-based breast cancer studies. By offering a holistic overview, it aims to support future research directions and encourage broader adoption of GAI technologies in healthcare. Additionally, the study emphasizes the importance of overcoming implementation barriers to fully realize GAI&#x2019;s potential in transforming breast cancer management.</p>
</abstract>
<kwd-group kwd-group-type="author">
<kwd>Breast cancer</kwd>
<kwd>generative AI</kwd>
<kwd>artificial intelligence</kwd>
<kwd>deep learning</kwd>
<kwd>diagnosis</kwd>
<kwd>treatment</kwd>
<kwd>oncology</kwd>
</kwd-group>
<funding-group>
<award-group id="awg1">
<funding-source>Fundamental Research Grant Scheme (FRGS)</funding-source>
<award-id>FRGS/1/2024/ICT02/TARUMT/02/1</award-id>
</award-group>
<award-group id="awg2">
<funding-source>Tunku Abdul Rahman University of Management and Technology (TAR UMT)</funding-source>
<award-id>UC/I/G2024-00129</award-id>
</award-group>
</funding-group>
</article-meta>
</front>
<body>
<sec id="s1">
<label>1</label>
<title>Introduction</title>
<p>GAI, a term that has gained attention recently across a wide spectrum of applications and domains, from experts to layman, from working adults to schooling children, regardless of formal working and/or leisure entertainment purposes, as well as daily errand planning. The emergence of consumer-facing products, for example, ChatGPT [<xref ref-type="bibr" rid="ref-1">1</xref>], StyleGAN [<xref ref-type="bibr" rid="ref-2">2</xref>], and/or MidJourney (AI image generator from text) [<xref ref-type="bibr" rid="ref-3">3</xref>] have revolutionizing the approaches of problem-solving amongst consumers in different facets of daily life. In clinical settings, GAI is not new however, some renowned architectures, for example, Generative Adversarial Networks (GAN), Recurrent Neural Networks (RNN), and Variational Autoencoders (VAE) have been used for decades in medical image analysis [<xref ref-type="bibr" rid="ref-4">4</xref>&#x2013;<xref ref-type="bibr" rid="ref-6">6</xref>], diagnostic and treatment of cancers, as well as laboratory-related applications. These architectures are less scalable, compared to the state-of-the-art models, which have traditionally restricted their development to smaller scales in terms of parameters, data, and computational resources, formalizing the foundation models for modern architectures in GAI.</p>
<p>AI, the umbrella term that encompasses all computational algorithms with capabilities to perform task-specific activities that conventionally require human intelligence, for example, decision-making, pattern recognition, and learning from past experiences. The idea of mimicking human intelligence was first conceived by Alan Turing in 1950 [<xref ref-type="bibr" rid="ref-7">7</xref>] and later the phrase: &#x201C;artificial intelligence&#x201D;, was coined by John McCarthy in 1956, specifically to remark an important subject area in science and engineering, as a sub-element of machine intelligence [<xref ref-type="bibr" rid="ref-8">8</xref>]. Early AI systems, which are commonly regarded as expert systems, are mainly knowledge-driven where well-defined rules are used as the backbone of the system [<xref ref-type="bibr" rid="ref-9">9</xref>&#x2013;<xref ref-type="bibr" rid="ref-11">11</xref>]. Thanks to the advancement in computational engineering, deep learning, a sub-element of AI, has made great strides in unsupervised learning of features from the sample/training datasets while performing task-specific activities (e.g., pattern recognition) automatically with promising performance that matches or even surpasses human performance [<xref ref-type="bibr" rid="ref-12">12</xref>]. <xref ref-type="fig" rid="fig-13">Fig. A1</xref> in <xref ref-type="sec" rid="app-1">Appendix A</xref> shows a brief timeline of AI advancement, while <xref ref-type="fig" rid="fig-1">Fig. 1</xref> shows the Venn diagram of AI and the respective sub-elements.</p>
<fig id="fig-1">
<label>Figure 1</label>
<caption>
<title>Venn diagram of AI and the respective sub-elements</title>
</caption>
<graphic mimetype="image" mime-subtype="tif" xlink:href="CMC_63407-fig-1.tif"/>
</fig>
<p>In deep learning, the two primary models are discriminative and generative models (the main focus of this study). Understanding the differences between these two models is essential, as each serves distinct purposes and approaches within the field of AI, particularly in breast cancer research. A discriminative model is intended to model and formalize the relationship between the input features (i.e., learned features) and the output labels (i.e., detection results). A generative model however learns from the inherent dataset and focuses on the probabilistic generation of new outputs, instead of providing decisions on extant data, for example, classification and clustering of extant data. Unlike the discriminative model, the outputs from the GAI are often not replicable, such that the same prompt may result in different solutions. These solutions however remain valid, fulfilling the input prompt from the users. Therefore, the utilization of discriminative and generative models in clinical settings are different but complement one another. In breast cancer, discriminative models (e.g., convolutional neural networks) are widely used in detection and classification activities, for example, benign and malignant breast cancer classification [<xref ref-type="bibr" rid="ref-13">13</xref>&#x2013;<xref ref-type="bibr" rid="ref-15">15</xref>]; prognosis and risk prediction typically on the likelihood of breast cancer recurrence or progression based on patient data [<xref ref-type="bibr" rid="ref-16">16</xref>,<xref ref-type="bibr" rid="ref-17">17</xref>]; outcome predictions that aid in predicting outcomes based on clinical, imaging, or genomic data [<xref ref-type="bibr" rid="ref-18">18</xref>], allowing clinicians to adjust treatment plans dynamically; and therapy optimization, for example, optimizing radiation or chemotherapy dosages by learning patterns in past treatment data [<xref ref-type="bibr" rid="ref-19">19</xref>,<xref ref-type="bibr" rid="ref-20">20</xref>]. Whereas GAI models (e.g., GAN) are often used in generative-oriented activities where creation or synthesis events are genuinely required, fulfilling the input prompt. GAI can improve breast lesion detection [<xref ref-type="bibr" rid="ref-21">21</xref>], facilitate image synthesis and data augmentation to generate augment datasets for training purposes [<xref ref-type="bibr" rid="ref-22">22</xref>,<xref ref-type="bibr" rid="ref-23">23</xref>], facilitate diagnosis and treatment procedures [<xref ref-type="bibr" rid="ref-24">24</xref>&#x2013;<xref ref-type="bibr" rid="ref-26">26</xref>], enhance the quality of breast medical images [<xref ref-type="bibr" rid="ref-27">27</xref>], and explore the drug structures and results validation [<xref ref-type="bibr" rid="ref-28">28</xref>]. <xref ref-type="fig" rid="fig-2">Fig. 2</xref> shows the general concept of discriminative and generative models in deep learning.</p>
<fig id="fig-2">
<label>Figure 2</label>
<caption>
<title>General concept of discriminative and generative models in deep learning (figure reproduced from [<xref ref-type="bibr" rid="ref-29">29</xref>] under Creative Commons CC BY license, Springer Nature)</title>
</caption>
<graphic mimetype="image" mime-subtype="tif" xlink:href="CMC_63407-fig-2.tif"/>
</fig>
<sec id="s1_1">
<label>1.1</label>
<title>Definition of GAI</title>
<p>In recent years, AI has become a ubiquitous term that is being used in a wide spectrum of domains with remarkable betterment. However, to adopt AI (or GAI) in the clinical setting, the system (so-called AI system) must be first defined and characterized, depending on the intended purposes associated with different risk categories. Defining AI systems is important, as this outlines clear boundaries and expectations for what the system is designed to do, how it operates, what the expected outcomes are, and the potential risks associated with it. Risk assessment is crucial, allowing users to understand, anticipate, and mitigate potential negative outcomes that could arise from AI usage, involving critical domains, for example, ethical consideration, safety and security, trust and public confidence, prevention of harm and legal risks, data privacy and security, as well as robustness and reliability. With the introduction of the AI Act, manufacturers are now required to identify which AI systems fall within the regulation scope and are consequently subject to act compliance and obligations. <xref ref-type="table" rid="table-1">Table 1</xref> shows the list of definitions of AI systems with respect to different sources.</p>
<table-wrap id="table-1">
<label>Table 1</label>
<caption>
<title>List of AI system definitions chronologically (table reproduced from [<xref ref-type="bibr" rid="ref-30">30</xref>] under Creative Commons CC BY license, Springer Nature)</title>
</caption>
<table>
<colgroup>
<col/>
<col/>
</colgroup>
<thead>
<tr align="center">
<th>Sources of definition</th>
<th>Definitions</th>
</tr>
</thead>
<tbody>
<tr align="center">
<td>The Organization for Economic Co-operation and Development (OECD) Recommendation of the Council on Artificial Intelligence 2019 [<xref ref-type="bibr" rid="ref-31">31</xref>]</td>
<td>&#x201C;<italic>An AI system is a machine-based system that can, for a given set of human-defined objectives, make predictions, recommendations, or decisions influencing real or virtual environments. AI systems are designed to operate with varying levels of autonomy</italic>&#x201D;</td>
</tr>
<tr align="center">
<td>Commission proposal&#x2014;(Art. 3(1)) [<xref ref-type="bibr" rid="ref-32">32</xref>]</td>
<td>&#x201C;<italic>AI system means software that is developed with one or more of the techniques and approaches listed in Annex I and can, for a given set of human-defined objectives, generate outputs such as content, predictions, recommendations, or decisions influencing the environments they interact with</italic>&#x201D;</td>
</tr>
<tr align="center">
<td>Council General Approach&#x2014;(Art. 3(1)) [<xref ref-type="bibr" rid="ref-33">33</xref>]</td>
<td>&#x201C;<italic>AI system means a system that is designed to operate with elements of autonomy and that, based on machine and/or human-provided data and inputs, infers how to achieve a given set of objectives using machine learning and/or logic- and knowledge based approaches, and produces system-generated outputs such as content (generative AI systems), predictions, recommendations or decisions, influencing the environments with which the AI system interacts</italic>&#x201D;</td>
</tr>
<tr align="center">
<td>European Parliament position&#x2014;(Art. 3(1)) [<xref ref-type="bibr" rid="ref-34">34</xref>]</td>
<td><italic>&#x201C;AI system means a machine-based system that is designed to operate with varying levels of autonomy and that can, for explicit or implicit objectives, generate outputs such as predictions, recommendations, or decisions, that influence physical or virtual environments</italic>&#x201D;</td>
</tr>
<tr align="center">
<td>OECD Recommendation of the Council on Artificial Intelligence 2023 [<xref ref-type="bibr" rid="ref-35">35</xref>,<xref ref-type="bibr" rid="ref-36">36</xref>]</td>
<td>&#x201C;<italic>An AI system is a machine-based system that, for explicit or implicit objectives, infers, from the input it receives, how to generate outputs such as predictions, content, recommendations, or decisions that can influence physical or virtual environments. Different AI systems vary in their levels of autonomy and adaptiveness after deployment</italic>&#x201D;</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
<sec id="s1_2">
<label>1.2</label>
<title>Classification of GAI</title>
<p><xref ref-type="fig" rid="fig-3">Fig. 3</xref> shows the classification of models in GAI, highlighting the respective architecture component and training method in each model. The architecture component defines how a model processes information and subsequently generates outputs, while the training method shapes the performance and effectiveness of a model.</p>
<fig id="fig-3">
<label>Figure 3</label>
<caption>
<title>Classification of GAI models (figure adapted from [<xref ref-type="bibr" rid="ref-40">40</xref>&#x2013;<xref ref-type="bibr" rid="ref-44">44</xref>] under Creative Commons CC BY license, MDPI), where &#x201C;&#x2297;&#x201D; and &#x201C;&#x2205;&#x201D; denote architecture components and training methods, respectively</title>
</caption>
<graphic mimetype="image" mime-subtype="tif" xlink:href="CMC_63407-fig-3.tif"/>
</fig>
<p>Briefly, the architecture of VAE is based on an encoder-decoder structure and uses variational inference in the training process [<xref ref-type="bibr" rid="ref-37">37</xref>,<xref ref-type="bibr" rid="ref-38">38</xref>]. VAEs are designed to learn compressed representations of input data by mapping it to a latent space. In the latent space, new samples can be generated by sampling and decoding from the learned distribution. A key highlight of VAEs is that the model incorporates a probabilistic framework, allowing them to generate diverse samples by drawing from a distribution rather than a fixed point, thus, making VAEs particularly suitable for tasks where a variety of output options is desirable, such as generating new images, reconstructing missing data, and/or performing anomaly detection.</p>
<p>GAN consists of two main components, namely, the generator and the discriminator. The primary role of the generator is to produce synthetic samples, for example, images, to deceive the discriminator, which evaluates whether a given sample is real or fake [<xref ref-type="bibr" rid="ref-39">39</xref>]. These two networks are trained adversarially, with the generator improving its output to fool the discriminator, and the discriminator improves capability in detecting fakes, formalizing a competition between the two leads (i.e., generator and discriminator), ultimately yielding highly realistic and diverse data. GANs have proven effective in areas, for example, image generation, video synthesis, and music composition. Despite their impressive results, GANs are known for being challenging to train, often requiring careful balancing between the generator and the discriminator to avoid issues like mode collapse.</p>
<p>Diffusion models involve a unique approach that starts with noisy data and progressively refines it through iterative denoising steps, which generate high-quality samples [<xref ref-type="bibr" rid="ref-41">41</xref>]. These models are trained by learning the dynamics of this noise-diffusion process, making them highly effective at tasks requiring precise, fine-grained detail, such as high-resolution image synthesis. The noising step inputs random noise into the data, and the denoising step gradually reconstructs the original signal through multiple iterations. Diffusion models have recently gained attention for their ability to outperform GANs in certain image generation tasks, specifically, in tasks in which the generation of detailed textures is required and successfully addresses some of the training instabilities seen in GANs.</p>
<p>Transformers employ an encoder-decoder architecture and make extensive use of self-attention mechanisms, which allow the model to capture long-range dependencies within data sequences [<xref ref-type="bibr" rid="ref-42">42</xref>]. Transformers are specifically effective in tasks that involve sequence data, for example, natural language processing, where the generation of coherent text or translation between languages is involved. The self-attention mechanism helps the model focus on relevant parts of the input sequence, making it highly scalable and efficient for tasks that involve handling large datasets with complex relationships. Notably, transformer models like Generative Pre-trained Transformers (GPTs) have demonstrated groundbreaking performance in text generation, translation, and summarization tasks.</p>
<p>Language models are typically built using RNNs or Long Short-Term Memory (LSTM) networks, which are designed to handle sequential data by predicting the next token in a sequence [<xref ref-type="bibr" rid="ref-43">43</xref>]. These models are trained through supervised learning and are specifically well-suited for generating natural language text, for example, completing sentences or writing paragraphs. The ability of language models to predict the next word in a sequence makes them crucial in applications like chatbots, translation systems, and automated content creation. With the rise of transformer-based models, language models have achieved even greater performance in generating coherent and contextually accurate text.</p>
<p>Normalizing Flow models use a sequence of invertible transformations, namely coupling layers, to transform data into a simpler distribution, for example, Gaussian distribution [<xref ref-type="bibr" rid="ref-44">44</xref>]. The key highlight of the normalizing flows is that the model preserves the exact probability density, allowing for accurate learning of complex distributions. By retaining density information in the data transformation process, this model is particularly suitable for tasks, for example, density estimation and probabilistic modeling. Normalizing Flow models are trained using maximum-likelihood estimation, making them useful in applications that require precise probability estimates, for example, anomaly detection or uncertainty quantification.</p>
<p>Hybrid models combine elements from multiple GAI models, allowing them to leverage the strengths of different models [<xref ref-type="bibr" rid="ref-40">40</xref>]. For example, a hybrid model can integrate the probabilistic sampling capabilities of VAEs with the adversarial training of GANs to achieve both diversity and realism in generated samples. By combining different architectures and training methods, hybrid models offer flexibility and can be tailored to meet specific generative goals, whether for image synthesis, text generation, or other creative tasks. These models are often designed to overcome the limitations of individual architectures, providing a more robust solution to GAI challenges.</p>
</sec>
<sec id="s1_3">
<label>1.3</label>
<title>Aims and Outline of the Study</title>
<p>Motivated by vigorous advancement in computation engineering and tremendous growth in world interest using GAI in breast cancer research, here, a systematic bibliographic survey focusing on GAI in breast cancer is presented. To ensure optimal search, no limiter is set on the publication year. The primary research questions of this study are: &#x201C;What are the applications and impacts of generative AI in breast cancer diagnosis and treatment?&#x201D; and &#x201C;How has generative AI been utilized to enhance outcomes in breast cancer research, particularly in predictive modeling, diagnostics, and therapeutic development?&#x201D;. The research question is framed as such to ensure the inclusion of all aspects of GAI models available within breast cancer. The present study is intended to focus on collating and synthesizing new insights and drawing constructive conclusions while highlighting the research gaps and challenges in the topic of interest. This study is organized as follows: <xref ref-type="sec" rid="s2">Section 2</xref> offers an overview of breast cancer diagnosis and treatment. <xref ref-type="sec" rid="s3">Section 3</xref> details the methodology employed in this systematic review. <xref ref-type="sec" rid="s4">Section 4</xref> presents synthesized findings from the included studies. <xref ref-type="sec" rid="s5">Section 5</xref> discusses self-assessment, limitations, challenges, and future directions. Finally, the conclusion is presented in <xref ref-type="sec" rid="s6">Section 6</xref>.</p>
</sec>
</sec>
<sec id="s2">
<label>2</label>
<title>Brief Descriptions of Diagnosis and Treatment of Breast Cancer</title>
<p>Here, the study primarily focuses on the diagnosis and treatment of breast cancer, formalizing the two main domains in cancer management. Diagnosis of breast cancer refers to the process of identifying the presence of cancer in the breast. This typically involves various tests and procedures, for example, clinical breast examination, breast imaging procedure, and biopsy grading [<xref ref-type="bibr" rid="ref-12">12</xref>,<xref ref-type="bibr" rid="ref-45">45</xref>]. In breast imaging procedures, imaging modalities such as non-ionizing radiation, gamma radiation (nuclear medicine), X-ray source, magnetic field, and ultrasound wave are commonly used [<xref ref-type="bibr" rid="ref-8">8</xref>,<xref ref-type="bibr" rid="ref-46">46</xref>]. Diagnosis of breast cancer is mainly to detect abnormal cells or tumors, determine their type, size, and stage, and assess whether the cancer has spread.</p>
<p>Treatment in breast cancer involves the medical management of the disease, including a combination of therapies, for example, surgery, chemotherapy, radiation therapy, hormone therapy, and targeted therapies. The choice of treatment is dependent on multi-facet factors, for example, the type and stage of the cancer, hormone receptor status, and overall health of the patient. The primary goal is to remove and/or destroy cancer cells and prevent recurrence. Briefly, some of the novel treatments, approved by the Food and Drug Administration (FDA) as targeted therapies for breast cancer are anti-estrogen, LH-RH analogs (goserelin and leuprolide), CDK4/6 inhibitor (Ribociclib, Palbociclib, and Abemaciclib), PI3Ki inhibitor (Pictilisib, Pilaralisib, and Voxtalisib), pan-PI3K inhibitor (Buparlisib), TKI (Neratinib and Lapatinib), and mAb [<xref ref-type="bibr" rid="ref-47">47</xref>].</p>
</sec>
<sec id="s3">
<label>3</label>
<title>Methods</title>
<p>The present study follows the PRISMA guidelines [<xref ref-type="bibr" rid="ref-48">48</xref>]. The review methodologies herein are adopted and adapted from the previously published protocol/works [<xref ref-type="bibr" rid="ref-49">49</xref>].</p>
<sec id="s3_1">
<label>3.1</label>
<title>Information Sources and Search Strategy</title>
<p>The proposed search strategies are the output of collaborative discussion from a team comprised of engineering and medical experts. As the present study focuses on generative AI in breast cancer, the search strings included two elements: &#x201C;generative AI&#x201D; and &#x201C;breast cancer&#x201D;. These elements are intentionally formulated in a broad manner to ensure optimal inclusion of data from all aspects (including diagnosis and treatment) that primarily adopt/integrate generative AI in breast cancer. The search strategies included limiters, for example, English language and journal articles. No limiter is set on publication years to maximize the data retrieved. The &#x2018;&#x2018;AND&#x201D; and &#x2018;&#x2018;OR&#x201D; operators were used to formalize the search string in the present study (see <xref ref-type="table" rid="table-2">Table 2</xref>). The systematic literature searches were last performed in December 2024 in four core databases: Scopus, Web of Science Core Collection, and PubMed, in lieu of search engines provided by specific publishers, such as SpringerLink, ScienceDirect, Multidisciplinary Digital Publishing Institute (MDPI), and Frontiers. Mendeley reference management software was used for reference management and related purposes.</p>
<table-wrap id="table-2">
<label>Table 2</label>
<caption>
<title>Search string</title>
</caption>
<table>
<colgroup>
<col/>
<col/>
<col/>
</colgroup>
<thead>
<tr align="center">
<th>Operator</th>
<th>Broad elements</th>
<th>Keywords and alternative phrases</th>
</tr>
</thead>
<tbody>
<tr align="center">
<td>AND</td>
<td>GAI</td>
<td>Generative AND artificial AND intelligence OR generative AND ai</td>
</tr>
<tr align="center">
<td></td>
<td>Breast cancer</td>
<td>Breast AND cancer</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
<sec id="s3_2">
<label>3.2</label>
<title>Eligibility Criteria</title>
<sec id="s3_2_1">
<label>3.2.1</label>
<title>Inclusion Criteria</title>
<p>Eligible studies were English-language original peer-reviewed journal research articles. Once a relevant journal research article was retrieved, the references of the articles were screened to explore potential articles that had not been identified in the initial search. This procedure iterates until no further articles are found. In Phase 1, only original peer-reviewed journal research articles were considered eligible. In Phase 2, screening was done on the abstract of the articles. The eligible materials were then subjected to full-text screening. In the full-text screening phase, a dual-independent approach was adopted, such that all articles were screened by two independent reviewers where the reviewers were blinded to the other&#x2019;s decision. If necessary, a discussion is held between the independent reviewers for eligibility evaluation, especially when the articles partially fulfill the inclusion criteria. If required, a third reviewer was consulted to attain consensus. The main inclusion criteria are: (1) the journal articles were using generative AI and (2) the journal articles were focusing on breast cancer (or multiple cancers that must include breast cancer). The last search of this study was performed on 24 December 2024. <xref ref-type="fig" rid="fig-4">Fig. 4</xref> summarizes the flowchart of the systematic search process in accordance with the PRISMA guideline [<xref ref-type="bibr" rid="ref-48">48</xref>]. Based on the flowchart, using the search strings as in <xref ref-type="table" rid="table-2">Table 2</xref>, a total of 3827 articles were first identified. Implementation of exclusion criteria of Phases 1 and 2, resulting in 31 articles eligible for the subsequent synthesis stage. In Phase 1, a total of 39 articles were excluded, whereas in Phase 2, only 4 articles were excluded. The complete PRISMA checklist is detailed in <xref ref-type="table" rid="table-7">Tables A2</xref> and <xref ref-type="table" rid="table-8">A3</xref> in <xref ref-type="sec" rid="app-3">Appendix C.</xref></p>
<fig id="fig-4">
<label>Figure 4</label>
<caption>
<title>Flowchart of the systematic search in accordance with the PRISMA guideline [<xref ref-type="bibr" rid="ref-48">48</xref>]</title>
</caption>
<graphic mimetype="image" mime-subtype="tif" xlink:href="CMC_63407-fig-4.tif"/>
</fig>
</sec>
<sec id="s3_2_2">
<label>3.2.2</label>
<title>Exclusion Criteria</title>
<p>Articles published in non-English languages were excluded. Materials, for example, master&#x2019;s and doctoral theses or dissertations, books, book chapters, grey literature, conference papers, review articles, application notes, brief communications, tutorials, and duplicate works were excluded. Protocol articles were securitized separately for eligibility. Protocol articles that solely reported methodology and protocol in breast cancer, with no study outcomes, were excluded.</p>
</sec>
</sec>
<sec id="s3_3">
<label>3.3</label>
<title>Data Extraction</title>
<p>Qualitative and quantitative data from each included article were carefully distilled and systematized into a functional summary endpoint. Qualitative data, for example, type of modalities, dataset, methods, and findings were extracted, compiled, and tabulated using a table. Quantitative data, for example, statistical findings, co-occurrence analysis, and bibliometric information, were collated and systematized to offer a holistic view of the topic of interest. Charts, graphics, and tables were used as a medium to synthesize the mineable data. For all included articles, the affiliation and author name were manually disambiguated (for example, &#x201C;Harvard Medical School&#x201D; and &#x201C;HMS&#x201D; are both referring to the same affiliation) to avoid duplication in the analysis using software such as VOS Viewer [<xref ref-type="bibr" rid="ref-50">50</xref>].</p>
</sec>
<sec id="s3_4">
<label>3.4</label>
<title>Results Synthesis</title>
<p>Qualitative and quantitative findings from the included works were reported narratively via the descriptive approach, supported using charts, graphics, and tables. Statistical calculations and compilation of data were done using Microsoft Excel 2019. Co-occurrence analysis and bibliometric findings were generated using VOS Viewer 1.6.20 software for Windows [<xref ref-type="bibr" rid="ref-50">50</xref>]. Quantitative findings, for example, classification of included works was illustrated using a pie chart; geographical distribution was illustrated using a world map chart; distribution of most contributing journals and publishers using bar charts; temporal publication analysis using a line graph; subject profiling using a treemap; and keywords co-occurrence, co-authorship occurrence, and country-ship analysis using bibliometric networks.</p>
</sec>
<sec id="s3_5">
<label>3.5</label>
<title>Definition of Performance Metrics Used in the Literature</title>
<p>The confusion matrix is one of the most commonly used performance metrics from the body of the literature, which is specifically useful in summarizing the classification performance of a classifier with respect to the testing/validating data. Typically, the confusion matrix consists of a two-dimensional matrix, where one axis represents the true class of an object, and the other represents the class predicted by the classifier. <xref ref-type="table" rid="table-3">Table 3</xref> provides an example of a confusion matrix for a three-class classification task with classes A, B, and C. The first row of the matrix indicates that 15 objects belong to class A, with 12 correctly classified as A, one misclassified as B, and two as C.</p>
<table-wrap id="table-3">
<label>Table 3</label>
<caption>
<title>Confusion matrix for three-class classification task</title>
</caption>
<table>
<colgroup>
<col align="center"/>
<col align="center"/>
<col align="center"/>
<col align="center"/>
<col align="center"/>
</colgroup>
<thead>
<tr align="center">
<th></th>
<th></th>
<th colspan="3">Assigned class</th>
</tr>
<tr align="center">
<th></th>
<th></th>
<th>A</th>
<th>B</th>
<th>C</th>
</tr>
</thead>
<tbody>
<tr align="center">
<td rowspan="3"><bold>Actual class</bold></td>
<td>A</td>
<td>12</td>
<td>1</td>
<td>2</td>
</tr>
<tr align="center">
<td>B</td>
<td>1</td>
<td>9</td>
<td>0</td>
</tr>
<tr align="center">
<td>C</td>
<td>0</td>
<td>0</td>
<td>6</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>In binary classification tasks, a simplified version of the confusion matrix is often used, where one class is designated as positive and the other as negative. The four cells of the matrix represent true positives (TP), false positives (FP), true negatives (TN), and false negatives (FN), as shown in <xref ref-type="table" rid="table-4">Table 4</xref>. Here, TP refers to the correctly predicted positive events, TN refers to the correctly predicted negative events, FP indicates the incorrectly predicted positive events, and FN represents the incorrectly predicted negative events.</p>
<table-wrap id="table-4">
<label>Table 4</label>
<caption>
<title>Confusion matrix for two-class classification task, classification into positive and negative classes</title>
</caption>
<table>
<colgroup>
<col align="center"/>
<col align="center"/>
<col align="center"/>
<col align="center"/>
</colgroup>
<thead>
<tr align="center">
<th></th>
<th></th>
<th colspan="2">Assigned class</th>
</tr>
<tr align="center">
<th></th>
<th></th>
<th>Positive</th>
<th>Negative</th>
</tr>
</thead>
<tbody>
<tr align="center">
<td rowspan="2"><bold>Actual class</bold></td>
<td><bold>Positive</bold></td>
<td>TP</td>
<td>FN</td>
</tr>
<tr align="center">
<td><bold>Negative</bold></td>
<td>FP</td>
<td>TN</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>From the obtained TP, TN, FP, and FN, performance metrics, for example, Accuracy, Recall/Sensitivity, Precision, Specificity, F1-score, and Area under the curve (AUC) can be computed. High values denote a better performance and are preferable in the study. The equations for Accuracy, Recall/Sensitivity, Precision, Specificity, F1-score, and AUC are as follows (<xref ref-type="disp-formula" rid="eqn-1">Eqs. (1)</xref>&#x2013;<xref ref-type="disp-formula" rid="eqn-6">(6)</xref>), where <italic>d</italic> in <xref ref-type="disp-formula" rid="eqn-6">Eq. (6)</xref> denotes the differential element (the small change) in the false positive rate (i.e., 1-Specificity).
<disp-formula id="eqn-1"><label>(1)</label><mml:math id="mml-eqn-1" display="block"><mml:mi>A</mml:mi><mml:mi>c</mml:mi><mml:mi>c</mml:mi><mml:mi>u</mml:mi><mml:mi>r</mml:mi><mml:mi>a</mml:mi><mml:mi>c</mml:mi><mml:mi>y</mml:mi><mml:mo>=</mml:mo><mml:mfrac><mml:mrow><mml:mi>T</mml:mi><mml:mi>P</mml:mi><mml:mo>+</mml:mo><mml:mi>T</mml:mi><mml:mi>N</mml:mi></mml:mrow><mml:mrow><mml:mi>T</mml:mi><mml:mi>P</mml:mi><mml:mo>+</mml:mo><mml:mi>T</mml:mi><mml:mi>N</mml:mi><mml:mo>+</mml:mo><mml:mi>F</mml:mi><mml:mi>P</mml:mi><mml:mo>+</mml:mo><mml:mi>F</mml:mi><mml:mi>N</mml:mi></mml:mrow></mml:mfrac></mml:math></disp-formula>
<disp-formula id="eqn-2"><label>(2)</label><mml:math id="mml-eqn-2" display="block"><mml:mi>R</mml:mi><mml:mi>e</mml:mi><mml:mi>c</mml:mi><mml:mi>a</mml:mi><mml:mi>l</mml:mi><mml:mi>l</mml:mi><mml:mrow><mml:mo>/</mml:mo></mml:mrow><mml:mi>S</mml:mi><mml:mi>e</mml:mi><mml:mi>n</mml:mi><mml:mi>s</mml:mi><mml:mi>i</mml:mi><mml:mi>t</mml:mi><mml:mi>i</mml:mi><mml:mi>v</mml:mi><mml:mi>i</mml:mi><mml:mi>t</mml:mi><mml:mi>y</mml:mi><mml:mo>=</mml:mo><mml:mfrac><mml:mrow><mml:mi>T</mml:mi><mml:mi>P</mml:mi></mml:mrow><mml:mrow><mml:mi>T</mml:mi><mml:mi>P</mml:mi><mml:mo>+</mml:mo><mml:mi>F</mml:mi><mml:mi>N</mml:mi></mml:mrow></mml:mfrac></mml:math></disp-formula>
<disp-formula id="eqn-3"><label>(3)</label><mml:math id="mml-eqn-3" display="block"><mml:mi>P</mml:mi><mml:mi>r</mml:mi><mml:mi>e</mml:mi><mml:mi>c</mml:mi><mml:mi>i</mml:mi><mml:mi>s</mml:mi><mml:mi>i</mml:mi><mml:mi>o</mml:mi><mml:mi>n</mml:mi><mml:mo>=</mml:mo><mml:mfrac><mml:mrow><mml:mi>T</mml:mi><mml:mi>P</mml:mi></mml:mrow><mml:mrow><mml:mi>T</mml:mi><mml:mi>P</mml:mi><mml:mo>+</mml:mo><mml:mi>F</mml:mi><mml:mi>P</mml:mi></mml:mrow></mml:mfrac></mml:math></disp-formula>
<disp-formula id="eqn-4"><label>(4)</label><mml:math id="mml-eqn-4" display="block"><mml:mi>S</mml:mi><mml:mi>p</mml:mi><mml:mi>e</mml:mi><mml:mi>c</mml:mi><mml:mi>i</mml:mi><mml:mi>f</mml:mi><mml:mi>i</mml:mi><mml:mi>c</mml:mi><mml:mi>i</mml:mi><mml:mi>t</mml:mi><mml:mi>y</mml:mi><mml:mo>=</mml:mo><mml:mfrac><mml:mrow><mml:mi>T</mml:mi><mml:mi>N</mml:mi></mml:mrow><mml:mrow><mml:mi>T</mml:mi><mml:mi>N</mml:mi><mml:mo>+</mml:mo><mml:mi>F</mml:mi><mml:mi>P</mml:mi></mml:mrow></mml:mfrac></mml:math></disp-formula>
<disp-formula id="eqn-5"><label>(5)</label><mml:math id="mml-eqn-5" display="block"><mml:mi>F</mml:mi><mml:mn>1</mml:mn><mml:mo>&#x2212;</mml:mo><mml:mi>s</mml:mi><mml:mi>c</mml:mi><mml:mi>o</mml:mi><mml:mi>r</mml:mi><mml:mi>e</mml:mi><mml:mo>=</mml:mo><mml:mfrac><mml:mrow><mml:mn>2</mml:mn><mml:mspace width="thinmathspace" /><mml:mo>&#x2217;</mml:mo><mml:mspace width="thinmathspace" /><mml:mi>R</mml:mi><mml:mi>e</mml:mi><mml:mi>c</mml:mi><mml:mi>a</mml:mi><mml:mi>l</mml:mi><mml:mi>l</mml:mi><mml:mspace width="thinmathspace" /><mml:mo>&#x2217;</mml:mo><mml:mspace width="thinmathspace" /><mml:mi>P</mml:mi><mml:mi>r</mml:mi><mml:mi>e</mml:mi><mml:mi>c</mml:mi><mml:mi>i</mml:mi><mml:mi>s</mml:mi><mml:mi>i</mml:mi><mml:mi>o</mml:mi><mml:mi>n</mml:mi></mml:mrow><mml:mrow><mml:mi>R</mml:mi><mml:mi>e</mml:mi><mml:mi>c</mml:mi><mml:mi>a</mml:mi><mml:mi>l</mml:mi><mml:mi>l</mml:mi><mml:mo>+</mml:mo><mml:mi>P</mml:mi><mml:mi>r</mml:mi><mml:mi>e</mml:mi><mml:mi>c</mml:mi><mml:mi>i</mml:mi><mml:mi>s</mml:mi><mml:mi>i</mml:mi><mml:mi>o</mml:mi><mml:mi>n</mml:mi></mml:mrow></mml:mfrac></mml:math></disp-formula>
<disp-formula id="eqn-6"><label>(6)</label><mml:math id="mml-eqn-6" display="block"><mml:mi>A</mml:mi><mml:mi>U</mml:mi><mml:mi>C</mml:mi><mml:mo>=</mml:mo><mml:msubsup><mml:mo>&#x222B;</mml:mo><mml:mrow><mml:mn>0</mml:mn></mml:mrow><mml:mrow><mml:mn>1</mml:mn></mml:mrow></mml:msubsup><mml:mi>R</mml:mi><mml:mi>e</mml:mi><mml:mi>c</mml:mi><mml:mi>a</mml:mi><mml:mi>l</mml:mi><mml:mi>l</mml:mi><mml:mo stretchy="false">(</mml:mo><mml:mn>1</mml:mn><mml:mo>&#x2212;</mml:mo><mml:mi>S</mml:mi><mml:mi>p</mml:mi><mml:mi>e</mml:mi><mml:mi>c</mml:mi><mml:mi>i</mml:mi><mml:mi>f</mml:mi><mml:mi>i</mml:mi><mml:mi>c</mml:mi><mml:mi>i</mml:mi><mml:mi>t</mml:mi><mml:mi>y</mml:mi><mml:mo stretchy="false">)</mml:mo><mml:mi>d</mml:mi><mml:mo stretchy="false">(</mml:mo><mml:mn>1</mml:mn><mml:mo>&#x2212;</mml:mo><mml:mi>S</mml:mi><mml:mi>p</mml:mi><mml:mi>e</mml:mi><mml:mi>c</mml:mi><mml:mi>i</mml:mi><mml:mi>f</mml:mi><mml:mi>i</mml:mi><mml:mi>c</mml:mi><mml:mi>i</mml:mi><mml:mi>t</mml:mi><mml:mi>y</mml:mi><mml:mo stretchy="false">)</mml:mo></mml:math></disp-formula></p>
<p>The <italic>p</italic>-value is a metric used in hypothesis testing to assess the statistical significance of an observed effect or outcome. It represents the probability of obtaining a test statistic as extreme as the one observed, assuming that the null hypothesis is true. The formula for calculating the <italic>p</italic>-value depends on the statistical test being used (e.g., z-test, <italic>t</italic>-test, chi-squared test, etc.). <xref ref-type="disp-formula" rid="eqn-7">Eqs. (7)</xref>&#x2013;<xref ref-type="disp-formula" rid="eqn-9">(9)</xref> show the formula for calculation of the two-tailed test (commonly known as the z-test or <italic>t</italic>-test), one-tailed test, and chi-squared test, respectively.
<disp-formula id="eqn-7"><label>(7)</label><mml:math id="mml-eqn-7" display="block"><mml:mi>p</mml:mi><mml:mo>=</mml:mo><mml:mn>2</mml:mn><mml:mo>&#x00D7;</mml:mo><mml:mi>P</mml:mi><mml:mo stretchy="false">(</mml:mo><mml:mi>Z</mml:mi><mml:mo>&#x2265;&#x2223;</mml:mo><mml:msub><mml:mi>z</mml:mi><mml:mrow><mml:mi>o</mml:mi><mml:mi>b</mml:mi><mml:mi>s</mml:mi></mml:mrow></mml:msub><mml:mo>&#x2223;</mml:mo><mml:mo stretchy="false">)</mml:mo></mml:math></disp-formula>where <inline-formula id="ieqn-1"><mml:math id="mml-ieqn-1"><mml:msub><mml:mi>z</mml:mi><mml:mrow><mml:mi>o</mml:mi><mml:mi>b</mml:mi><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:math></inline-formula> is the observed test statistic; <inline-formula id="ieqn-2"><mml:math id="mml-ieqn-2"><mml:mi>P</mml:mi><mml:mo stretchy="false">(</mml:mo><mml:mi>Z</mml:mi><mml:mo>&#x2265;&#x2223;</mml:mo><mml:msub><mml:mi>z</mml:mi><mml:mrow><mml:mi>o</mml:mi><mml:mi>b</mml:mi><mml:mi>s</mml:mi></mml:mrow></mml:msub><mml:mo>&#x2223;</mml:mo><mml:mo stretchy="false">)</mml:mo></mml:math></inline-formula> is the probability that a standard normal random variable exceeds the absolute value of the observed z-score (area under the tail).
<disp-formula id="eqn-8"><label>(8)</label><mml:math id="mml-eqn-8" display="block"><mml:mi>p</mml:mi><mml:mo>=</mml:mo><mml:mi>P</mml:mi><mml:mo stretchy="false">(</mml:mo><mml:mi>Z</mml:mi><mml:mo>&#x2265;</mml:mo><mml:msub><mml:mi>z</mml:mi><mml:mrow><mml:mi>o</mml:mi><mml:mi>b</mml:mi><mml:mi>s</mml:mi></mml:mrow></mml:msub><mml:mo stretchy="false">)</mml:mo></mml:math></disp-formula>where <inline-formula id="ieqn-3"><mml:math id="mml-ieqn-3"><mml:msub><mml:mi>z</mml:mi><mml:mrow><mml:mi>o</mml:mi><mml:mi>b</mml:mi><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:math></inline-formula> is the observed test statistic; <inline-formula id="ieqn-4"><mml:math id="mml-ieqn-4"><mml:mi>P</mml:mi><mml:mo stretchy="false">(</mml:mo><mml:mi>Z</mml:mi><mml:mo>&#x2265;</mml:mo><mml:msub><mml:mi>z</mml:mi><mml:mrow><mml:mi>o</mml:mi><mml:mi>b</mml:mi><mml:mi>s</mml:mi></mml:mrow></mml:msub><mml:mo stretchy="false">)</mml:mo></mml:math></inline-formula> is the probability corresponding to the test statistic under the null hypothesis.
<disp-formula id="eqn-9"><label>(9)</label><mml:math id="mml-eqn-9" display="block"><mml:mi>p</mml:mi><mml:mo>=</mml:mo><mml:mi>P</mml:mi><mml:mo stretchy="false">(</mml:mo><mml:msup><mml:mi>x</mml:mi><mml:mrow><mml:mn>2</mml:mn></mml:mrow></mml:msup><mml:mo>&#x2265;</mml:mo><mml:msubsup><mml:mi>x</mml:mi><mml:mrow><mml:mi>o</mml:mi><mml:mi>b</mml:mi><mml:mi>s</mml:mi></mml:mrow><mml:mrow><mml:mn>2</mml:mn></mml:mrow></mml:msubsup><mml:mo stretchy="false">)</mml:mo></mml:math></disp-formula>where <inline-formula id="ieqn-5"><mml:math id="mml-ieqn-5"><mml:msubsup><mml:mi>x</mml:mi><mml:mrow><mml:mi>o</mml:mi><mml:mi>b</mml:mi><mml:mi>s</mml:mi></mml:mrow><mml:mrow><mml:mn>2</mml:mn></mml:mrow></mml:msubsup></mml:math></inline-formula> is the observed chi-squared statistic; <inline-formula id="ieqn-6"><mml:math id="mml-ieqn-6"><mml:mi>P</mml:mi><mml:mo stretchy="false">(</mml:mo><mml:msup><mml:mi>x</mml:mi><mml:mrow><mml:mn>2</mml:mn></mml:mrow></mml:msup><mml:mo>&#x2265;</mml:mo><mml:msubsup><mml:mi>x</mml:mi><mml:mrow><mml:mi>o</mml:mi><mml:mi>b</mml:mi><mml:mi>s</mml:mi></mml:mrow><mml:mrow><mml:mn>2</mml:mn></mml:mrow></mml:msubsup><mml:mo stretchy="false">)</mml:mo></mml:math></inline-formula> is the probability under the chi-squared distribution. The <italic>p</italic>-value test is commonly used to determine whether to reject the null hypothesis (i.e., <inline-formula id="ieqn-7"><mml:math id="mml-ieqn-7"><mml:msub><mml:mi>H</mml:mi><mml:mrow><mml:mn>0</mml:mn></mml:mrow></mml:msub></mml:math></inline-formula>) in favor of the alternative hypothesis (i.e., <inline-formula id="ieqn-8"><mml:math id="mml-ieqn-8"><mml:msub><mml:mi>H</mml:mi><mml:mrow><mml:mn>1</mml:mn></mml:mrow></mml:msub></mml:math></inline-formula>). A small <italic>p</italic>-value, typically &#x2264;0.05, indicates that the observed data is unlikely under the null hypothesis, suggesting that the null hypothesis may be false, and the alternative hypothesis may be more plausible. Whereas, a large <italic>p</italic>-value, typically &#x003E;0.05 suggests that the observed data is consistent with the null hypothesis, hence, lack of evidence to reject the hypothesis.</p>
<p>Mean Squared Error (MSE) is a widely used metric for assessing the performance of regression models. It calculates the average of the squared differences between the actual values and the predicted values from the model. The MSE gauges how accurately the predicted values align with the true data points. It is always non-negative, with lower values indicating a better fit of the model to the data. Conversely, a higher MSE implies that the model&#x2019;s predictions are further from the actual values. The formula for MSE is shown in <xref ref-type="disp-formula" rid="eqn-10">Eq. (10)</xref>.
<disp-formula id="eqn-10"><label>(10)</label><mml:math id="mml-eqn-10" display="block"><mml:mi>M</mml:mi><mml:mi>S</mml:mi><mml:mi>E</mml:mi><mml:mo>=</mml:mo><mml:mfrac><mml:mn>1</mml:mn><mml:mi>n</mml:mi></mml:mfrac><mml:msubsup><mml:mo movablelimits="false">&#x2211;</mml:mo><mml:mrow><mml:mi>i</mml:mi><mml:mo>=</mml:mo><mml:mn>1</mml:mn></mml:mrow><mml:mrow><mml:mi>n</mml:mi></mml:mrow></mml:msubsup><mml:mo stretchy="false">(</mml:mo><mml:mrow><mml:msub><mml:mi>y</mml:mi><mml:mrow><mml:mi>i</mml:mi></mml:mrow></mml:msub></mml:mrow><mml:mo>&#x2212;</mml:mo><mml:mrow><mml:msub><mml:mrow><mml:mover><mml:mi>y</mml:mi><mml:mo stretchy="false">&#x005E;</mml:mo></mml:mover></mml:mrow><mml:mrow><mml:mi>i</mml:mi></mml:mrow></mml:msub></mml:mrow><mml:msup><mml:mo stretchy="false">)</mml:mo><mml:mrow><mml:mn>2</mml:mn></mml:mrow></mml:msup></mml:math></disp-formula>where <italic>n</italic> denotes the number of data points (sample size); <inline-formula id="ieqn-9"><mml:math id="mml-ieqn-9"><mml:msub><mml:mi>y</mml:mi><mml:mrow><mml:mi>i</mml:mi></mml:mrow></mml:msub></mml:math></inline-formula> denotes the actual/true value for the <italic>i</italic>-th data point; <inline-formula id="ieqn-10"><mml:math id="mml-ieqn-10"><mml:msub><mml:mrow><mml:mover><mml:mi>y</mml:mi><mml:mo stretchy="false">&#x005E;</mml:mo></mml:mover></mml:mrow><mml:mrow><mml:mi>i</mml:mi></mml:mrow></mml:msub></mml:math></inline-formula> denotes the predicted value for the <italic>i</italic>-th data point; <inline-formula id="ieqn-11"><mml:math id="mml-ieqn-11"><mml:munderover><mml:mo>&#x2211;</mml:mo><mml:mrow><mml:mi>i</mml:mi><mml:mo>=</mml:mo><mml:mn>1</mml:mn></mml:mrow><mml:mrow><mml:mi>n</mml:mi></mml:mrow></mml:munderover><mml:mo stretchy="false">(</mml:mo><mml:mrow><mml:msub><mml:mi>y</mml:mi><mml:mrow><mml:mi>i</mml:mi></mml:mrow></mml:msub></mml:mrow><mml:mo>&#x2212;</mml:mo><mml:mrow><mml:msub><mml:mrow><mml:mover><mml:mi>y</mml:mi><mml:mo stretchy="false">&#x005E;</mml:mo></mml:mover></mml:mrow><mml:mrow><mml:mi>i</mml:mi></mml:mrow></mml:msub></mml:mrow><mml:msup><mml:mo stretchy="false">)</mml:mo><mml:mrow><mml:mn>2</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> denotes the sum of the squared differences between the actual/true and predicted values. The difference calculation is computed for each data point, <italic>i</italic>, by calculating the difference between the actual value, <inline-formula id="ieqn-12"><mml:math id="mml-ieqn-12"><mml:msub><mml:mi>y</mml:mi><mml:mrow><mml:mi>i</mml:mi></mml:mrow></mml:msub></mml:math></inline-formula>, and the predicted value, <inline-formula id="ieqn-13"><mml:math id="mml-ieqn-13"><mml:msub><mml:mrow><mml:mover><mml:mi>y</mml:mi><mml:mo stretchy="false">&#x005E;</mml:mo></mml:mover></mml:mrow><mml:mrow><mml:mi>i</mml:mi></mml:mrow></mml:msub></mml:math></inline-formula>. The difference value is then squared to eliminate negative values and to give more weight to larger errors. The sum of these squared differences is averaged by dividing by the total number of data points, <italic>n</italic>, giving the mean squared error. Because the MSE equation involves a square of the differences between actual/true and predicted values, the MSE is then sensitive to outliers. MSE is often used to compare different models or algorithms by seeing which has the lowest error. A smaller MSE indicates better performance, with 0 being the ideal value, denoting no difference between predicted and actual/true values.</p>
<p>Intersection over Union (IoU) is a metric frequently used to assess the performance of object detection, segmentation, and other tasks that require evaluating the spatial overlap between predicted and ground truth regions. It quantifies the overlap between two areas, such as the predicted bounding box (or segmentation mask) and the ground truth bounding box (or mask). <xref ref-type="disp-formula" rid="eqn-11">Eq. (11)</xref> presents the IoU formula, where the Area of Overlap represents the region where the predicted and ground truth areas intersect (i.e., the shared portion of both regions), and the Area of Union refers to the total area covered by both the predicted and ground truth regions, excluding the overlap (i.e., the combined area of both regions).
<disp-formula id="eqn-11"><label>(11)</label><mml:math id="mml-eqn-11" display="block"><mml:mi>I</mml:mi><mml:mi>o</mml:mi><mml:mi>U</mml:mi><mml:mo>=</mml:mo><mml:mfrac><mml:mrow><mml:mi>A</mml:mi><mml:mi>r</mml:mi><mml:mi>e</mml:mi><mml:mi>a</mml:mi><mml:mspace width="thinmathspace" /><mml:mi>o</mml:mi><mml:mi>f</mml:mi><mml:mspace width="thinmathspace" /><mml:mi>O</mml:mi><mml:mi>v</mml:mi><mml:mi>e</mml:mi><mml:mi>r</mml:mi><mml:mi>l</mml:mi><mml:mi>a</mml:mi><mml:mi>p</mml:mi></mml:mrow><mml:mrow><mml:mi>A</mml:mi><mml:mi>r</mml:mi><mml:mi>e</mml:mi><mml:mi>a</mml:mi><mml:mspace width="thinmathspace" /><mml:mi>o</mml:mi><mml:mi>f</mml:mi><mml:mspace width="thinmathspace" /><mml:mi>U</mml:mi><mml:mi>n</mml:mi><mml:mi>i</mml:mi><mml:mi>o</mml:mi><mml:mi>n</mml:mi></mml:mrow></mml:mfrac></mml:math></disp-formula></p>
<p>The ideal IoU value is 1, indicating that the predicted region exactly matches the ground truth. To the opposite extreme (IoU of 0), the equation implies no overlap between the predicted and ground truth regions. Higher IoU is preferable in all cases, indicating better alignment between the predicted and actual regions, with values closer to 1 being ideal.</p>
<p>Mean IoU is an extension of IoU, mainly used for multi-class segmentation tasks. The Mean IoU computes the IoU for each class in a dataset and then takes the average over all classes. This gives a more comprehensive evaluation metric when dealing with multiple objects or regions across several classes. <xref ref-type="disp-formula" rid="eqn-12">Eq. (12)</xref> shows the formula of Mean IoU, such that <italic>C</italic> denotes the number of classes; Area of Overlap for Class <italic>i</italic> and Area of Union for Class <italic>i</italic> denote the overlap and union areas for class <italic>i</italic> across all images or regions in the dataset.
<disp-formula id="eqn-12"><label>(12)</label><mml:math id="mml-eqn-12" display="block"><mml:mi>M</mml:mi><mml:mi>e</mml:mi><mml:mi>a</mml:mi><mml:mi>n</mml:mi><mml:mspace width="thinmathspace" /><mml:mi>I</mml:mi><mml:mi>o</mml:mi><mml:mi>U</mml:mi><mml:mo>=</mml:mo><mml:mfrac><mml:mn>1</mml:mn><mml:mi>C</mml:mi></mml:mfrac><mml:munderover><mml:mo>&#x2211;</mml:mo><mml:mrow><mml:mi>i</mml:mi><mml:mo>=</mml:mo><mml:mn>1</mml:mn></mml:mrow><mml:mrow><mml:mi>C</mml:mi></mml:mrow></mml:munderover><mml:mfrac><mml:mrow><mml:mi>A</mml:mi><mml:mi>r</mml:mi><mml:mi>e</mml:mi><mml:mi>a</mml:mi><mml:mspace width="thinmathspace" /><mml:mi>o</mml:mi><mml:mi>f</mml:mi><mml:mspace width="thinmathspace" /><mml:mi>O</mml:mi><mml:mi>v</mml:mi><mml:mi>e</mml:mi><mml:mi>r</mml:mi><mml:mi>l</mml:mi><mml:mi>a</mml:mi><mml:mi>p</mml:mi><mml:mspace width="thinmathspace" /><mml:mi>f</mml:mi><mml:mi>o</mml:mi><mml:mi>r</mml:mi><mml:mspace width="thinmathspace" /><mml:mi>C</mml:mi><mml:mi>l</mml:mi><mml:mi>a</mml:mi><mml:mi>s</mml:mi><mml:mi>s</mml:mi><mml:mspace width="thinmathspace" /><mml:mi>i</mml:mi></mml:mrow><mml:mrow><mml:mi>A</mml:mi><mml:mi>r</mml:mi><mml:mi>e</mml:mi><mml:mi>a</mml:mi><mml:mspace width="thinmathspace" /><mml:mi>o</mml:mi><mml:mi>f</mml:mi><mml:mspace width="thinmathspace" /><mml:mi>U</mml:mi><mml:mi>n</mml:mi><mml:mi>i</mml:mi><mml:mi>o</mml:mi><mml:mi>n</mml:mi><mml:mspace width="thinmathspace" /><mml:mi>f</mml:mi><mml:mi>o</mml:mi><mml:mi>r</mml:mi><mml:mspace width="thinmathspace" /><mml:mi>C</mml:mi><mml:mi>l</mml:mi><mml:mi>a</mml:mi><mml:mi>s</mml:mi><mml:mi>s</mml:mi><mml:mspace width="thinmathspace" /><mml:mi>i</mml:mi></mml:mrow></mml:mfrac></mml:math></disp-formula></p>
<p>The Mean IoU calculates the IoU for each class independently and then averages the results across all classes. The equation is particularly useful in semantic segmentation, where you need to evaluate how well the model predicts boundaries across multiple classes. Higher Mean IoU indicates better segmentation performance, with values closer to 1 indicating near-perfect segmentation.</p>
<p>The Intraclass Correlation Coefficient (ICC) is a statistic used to assess the reliability or agreement between measurements made by different observers, instruments, or measurement methods. ICC is especially useful when the measurements are made on the same subjects or items and can be used to evaluate consistency or conformity within groups of measurements. The ICC is commonly used in domains, for example, medicine, psychology, and medical image analysis, where multiple measurements or ratings are obtained for the same subjects under different conditions.</p>
<p><xref ref-type="disp-formula" rid="eqn-13">Eq. (13)</xref> shows the general form of the ICC formula, such that ICC (1,1) assesses absolute agreement between raters or measurements; ICC (2,1) assesses consistency across raters when raters are considered interchangeable; and ICC (3,1) assesses reliability when specific raters or instruments are used and generalization to other raters is not desired.
<disp-formula id="eqn-13"><label>(13)</label><mml:math id="mml-eqn-13" display="block"><mml:mi>I</mml:mi><mml:mi>C</mml:mi><mml:mi>C</mml:mi><mml:mo>=</mml:mo><mml:mfrac><mml:mrow><mml:mi>B</mml:mi><mml:mi>e</mml:mi><mml:mi>t</mml:mi><mml:mi>w</mml:mi><mml:mi>e</mml:mi><mml:mi>e</mml:mi><mml:mi>n</mml:mi><mml:mspace width="thinmathspace" /><mml:mi>s</mml:mi><mml:mi>u</mml:mi><mml:mi>b</mml:mi><mml:mi>j</mml:mi><mml:mi>e</mml:mi><mml:mi>c</mml:mi><mml:mi>t</mml:mi><mml:mspace width="thinmathspace" /><mml:mi>v</mml:mi><mml:mi>a</mml:mi><mml:mi>r</mml:mi><mml:mi>i</mml:mi><mml:mi>a</mml:mi><mml:mi>n</mml:mi><mml:mi>c</mml:mi><mml:mi>e</mml:mi></mml:mrow><mml:mrow><mml:mi>B</mml:mi><mml:mi>e</mml:mi><mml:mi>t</mml:mi><mml:mi>w</mml:mi><mml:mi>e</mml:mi><mml:mi>e</mml:mi><mml:mi>n</mml:mi><mml:mspace width="thinmathspace" /><mml:mi>s</mml:mi><mml:mi>u</mml:mi><mml:mi>b</mml:mi><mml:mi>j</mml:mi><mml:mi>e</mml:mi><mml:mi>c</mml:mi><mml:mi>t</mml:mi><mml:mspace width="thinmathspace" /><mml:mi>v</mml:mi><mml:mi>a</mml:mi><mml:mi>r</mml:mi><mml:mi>i</mml:mi><mml:mi>a</mml:mi><mml:mi>n</mml:mi><mml:mi>c</mml:mi><mml:mi>e</mml:mi><mml:mo>+</mml:mo><mml:mi>W</mml:mi><mml:mi>i</mml:mi><mml:mi>t</mml:mi><mml:mi>h</mml:mi><mml:mi>i</mml:mi><mml:mi>n</mml:mi><mml:mspace width="thinmathspace" /><mml:mi>s</mml:mi><mml:mi>u</mml:mi><mml:mi>b</mml:mi><mml:mi>j</mml:mi><mml:mi>e</mml:mi><mml:mi>c</mml:mi><mml:mi>t</mml:mi><mml:mspace width="thinmathspace" /><mml:mi>v</mml:mi><mml:mi>a</mml:mi><mml:mi>r</mml:mi><mml:mi>i</mml:mi><mml:mi>a</mml:mi><mml:mi>n</mml:mi><mml:mi>c</mml:mi><mml:mi>e</mml:mi></mml:mrow></mml:mfrac></mml:math></disp-formula>where &#x201C;<italic>Between subject variance</italic>&#x201D; denotes the variation between different subjects or items being measured, and &#x201C;<italic>Within subject variance</italic>&#x201D; denotes the variation between repeated measurements or raters for the same subject. ICC is mainly used in measuring the consistency or reliability of a measurement across different raters or instruments or to determine the level of agreement across two or more raters who provide ratings or scores for the same subjects.</p>
<p>The Peak Signal-to-Noise Ratio (PSNR) is a commonly used metric in image processing to assess the quality of a reconstructed or compressed image in relation to its original version. It measures the degree of distortion caused by lossy compression or other image processing methods by comparing the original and modified images. PSNR is particularly valuable for evaluating image compression algorithms, such as those used for image restoration through denoising or super-resolution techniques. The formula for PSNR is shown in <xref ref-type="disp-formula" rid="eqn-14">Eq. (14)</xref>.
<disp-formula id="eqn-14"><label>(14)</label><mml:math id="mml-eqn-14" display="block"><mml:mi>P</mml:mi><mml:mi>S</mml:mi><mml:mi>N</mml:mi><mml:mi>R</mml:mi><mml:mo>=</mml:mo><mml:mn>10</mml:mn><mml:mo>&#x22C5;</mml:mo><mml:mi>l</mml:mi><mml:mi>o</mml:mi><mml:msub><mml:mi>g</mml:mi><mml:mrow><mml:mn>10</mml:mn></mml:mrow></mml:msub><mml:mfrac><mml:mrow><mml:mi>M</mml:mi><mml:mi>A</mml:mi><mml:msup><mml:mi>X</mml:mi><mml:mrow><mml:mn>2</mml:mn></mml:mrow></mml:msup></mml:mrow><mml:mrow><mml:mi>M</mml:mi><mml:mi>S</mml:mi><mml:mi>E</mml:mi></mml:mrow></mml:mfrac></mml:math></disp-formula>where <italic>MAX</italic> denotes the maximum possible pixel value of the image. PSNR helps determine how much distortion or noise is introduced when compressing an image and is extremely useful in measuring the effectiveness of methods, for example, denoising, deblurring, and other image reconstruction techniques. A high PSNR value indicates that the processed image is closer to the original image, with less noise or distortion, whereas a low PSNR value implies that the processed image has higher distortion/noise, making it less similar to the original.</p>
<p>The Structural Similarity Index (SSIM) is a metric used to evaluate the similarity between two images. Unlike traditional methods, for example, MSE or PSNR, which focus on pixel-level differences, SSIM assesses image quality by considering structural information, resembling human visual perception. It compares the luminance, contrast, and structure of the images to determine their similarity. SSIM is especially beneficial in image processing tasks like compression, denoising, and enhancement, where preserving structural integrity is essential. The formula for SSIM is presented in <xref ref-type="disp-formula" rid="eqn-15">Eq. (15)</xref>.
<disp-formula id="eqn-15"><label>(15)</label><mml:math id="mml-eqn-15" display="block"><mml:mi>S</mml:mi><mml:mi>S</mml:mi><mml:mi>I</mml:mi><mml:mi>M</mml:mi><mml:mrow><mml:mo>(</mml:mo><mml:mi>x</mml:mi><mml:mo>,</mml:mo><mml:mi>y</mml:mi><mml:mo>)</mml:mo></mml:mrow><mml:mo>=</mml:mo><mml:mfrac><mml:mrow><mml:mo stretchy="false">(</mml:mo><mml:mn>2</mml:mn><mml:msub><mml:mi>&#x03BC;</mml:mi><mml:mrow><mml:mi>x</mml:mi></mml:mrow></mml:msub><mml:msub><mml:mi>&#x03BC;</mml:mi><mml:mrow><mml:mi>y</mml:mi></mml:mrow></mml:msub><mml:mo>+</mml:mo><mml:msub><mml:mi>C</mml:mi><mml:mrow><mml:mn>1</mml:mn></mml:mrow></mml:msub><mml:mo stretchy="false">)</mml:mo><mml:mo stretchy="false">(</mml:mo><mml:mn>2</mml:mn><mml:msub><mml:mi>&#x03C3;</mml:mi><mml:mrow><mml:mi>x</mml:mi><mml:mi>y</mml:mi></mml:mrow></mml:msub><mml:mo>+</mml:mo><mml:msub><mml:mi>C</mml:mi><mml:mrow><mml:mn>2</mml:mn></mml:mrow></mml:msub><mml:mo stretchy="false">)</mml:mo></mml:mrow><mml:mrow><mml:mo stretchy="false">(</mml:mo><mml:msubsup><mml:mi>&#x03BC;</mml:mi><mml:mrow><mml:mi>x</mml:mi></mml:mrow><mml:mrow><mml:mn>2</mml:mn></mml:mrow></mml:msubsup><mml:mo>+</mml:mo><mml:msubsup><mml:mi>&#x03BC;</mml:mi><mml:mrow><mml:mi>y</mml:mi></mml:mrow><mml:mrow><mml:mn>2</mml:mn></mml:mrow></mml:msubsup><mml:mo>+</mml:mo><mml:msub><mml:mi>C</mml:mi><mml:mrow><mml:mn>1</mml:mn></mml:mrow></mml:msub><mml:mo stretchy="false">)</mml:mo><mml:mo stretchy="false">(</mml:mo><mml:msubsup><mml:mi>&#x03C3;</mml:mi><mml:mrow><mml:mi>x</mml:mi></mml:mrow><mml:mrow><mml:mn>2</mml:mn></mml:mrow></mml:msubsup><mml:mo>+</mml:mo><mml:msubsup><mml:mi>&#x03C3;</mml:mi><mml:mrow><mml:mi>y</mml:mi></mml:mrow><mml:mrow><mml:mn>2</mml:mn></mml:mrow></mml:msubsup><mml:mo>+</mml:mo><mml:msub><mml:mi>C</mml:mi><mml:mrow><mml:mn>2</mml:mn></mml:mrow></mml:msub><mml:mo stretchy="false">)</mml:mo></mml:mrow></mml:mfrac></mml:math></disp-formula>where <inline-formula id="ieqn-14"><mml:math id="mml-ieqn-14"><mml:msub><mml:mi>&#x03BC;</mml:mi><mml:mrow><mml:mi>x</mml:mi></mml:mrow></mml:msub></mml:math></inline-formula> and <inline-formula id="ieqn-15"><mml:math id="mml-ieqn-15"><mml:msub><mml:mi>&#x03BC;</mml:mi><mml:mrow><mml:mi>y</mml:mi></mml:mrow></mml:msub></mml:math></inline-formula> denote the means (average pixel intensity) of images <italic>x</italic> and <italic>y</italic>, representing luminance; <inline-formula id="ieqn-16"><mml:math id="mml-ieqn-16"><mml:msubsup><mml:mi>&#x03C3;</mml:mi><mml:mrow><mml:mi>x</mml:mi></mml:mrow><mml:mrow><mml:mn>2</mml:mn></mml:mrow></mml:msubsup></mml:math></inline-formula> and <inline-formula id="ieqn-17"><mml:math id="mml-ieqn-17"><mml:msubsup><mml:mi>&#x03C3;</mml:mi><mml:mrow><mml:mi>y</mml:mi></mml:mrow><mml:mrow><mml:mn>2</mml:mn></mml:mrow></mml:msubsup></mml:math></inline-formula> denote the variances of <italic>x</italic> and <italic>y</italic>, representing the contrast; <inline-formula id="ieqn-18"><mml:math id="mml-ieqn-18"><mml:msub><mml:mi>&#x03C3;</mml:mi><mml:mrow><mml:mi>x</mml:mi><mml:mi>y</mml:mi></mml:mrow></mml:msub></mml:math></inline-formula> denotes the covariance between <italic>x</italic> and <italic>y</italic>, representing the correlation in structure between the images. When the SSIM equals to 1, the images are identical in terms of luminance, contrast, and structure; when the SSIM equals to 0, no structural similarity between the images. Thus, an SSIM value closer to 1 implies higher structural similarity, denoting that the processed image retains more of the original&#x2019;s structural features.</p>
<p>The Kappa Value, also known as Cohen&#x2019;s Kappa, is a statistical metric used to measure the degree of agreement between two raters or evaluators who categorize items into distinct groups. It is particularly valuable when assessing how well two different observers align in classifying the same items while accounting for the likelihood of agreement occurring by chance. Cohen&#x2019;s Kappa quantifies the level of agreement between the two classifications, offering insight into whether the observed agreement surpasses what would be expected randomly. This metric is widely used in fields like psychology, medicine, and social sciences to assess the reliability of observers or raters. The formula for Cohen&#x2019;s Kappa is shown in <xref ref-type="disp-formula" rid="eqn-16">Eq. (16)</xref>.
<disp-formula id="eqn-16"><label>(16)</label><mml:math id="mml-eqn-16" display="block"><mml:mi>C</mml:mi><mml:mi>o</mml:mi><mml:mi>h</mml:mi><mml:mi>e</mml:mi><mml:msup><mml:mi>n</mml:mi><mml:mrow><mml:mi mathvariant="normal">&#x2032;</mml:mi></mml:mrow></mml:msup><mml:mi>s</mml:mi><mml:mspace width="thinmathspace" /><mml:mi>K</mml:mi><mml:mi>a</mml:mi><mml:mi>p</mml:mi><mml:mi>p</mml:mi><mml:mi>a</mml:mi><mml:mo>=</mml:mo><mml:mfrac><mml:mrow><mml:msub><mml:mi>P</mml:mi><mml:mrow><mml:mn>0</mml:mn></mml:mrow></mml:msub><mml:mo>&#x2212;</mml:mo><mml:msub><mml:mi>P</mml:mi><mml:mrow><mml:mi>e</mml:mi></mml:mrow></mml:msub></mml:mrow><mml:mrow><mml:mn>1</mml:mn><mml:mo>&#x2212;</mml:mo><mml:msub><mml:mi>P</mml:mi><mml:mrow><mml:mi>e</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mfrac></mml:math></disp-formula>where <inline-formula id="ieqn-19"><mml:math id="mml-ieqn-19"><mml:msub><mml:mi>P</mml:mi><mml:mrow><mml:mn>0</mml:mn></mml:mrow></mml:msub></mml:math></inline-formula> denotes the observed agreement, computed based on the proportion of times the raters agree (the total number of agreements divided by the total number of observations); <inline-formula id="ieqn-20"><mml:math id="mml-ieqn-20"><mml:msub><mml:mi>P</mml:mi><mml:mrow><mml:mi>e</mml:mi></mml:mrow></mml:msub></mml:math></inline-formula> denotes the expected agreement, computed based on the proportion of times the raters would be expected to agree by chance. The <inline-formula id="ieqn-21"><mml:math id="mml-ieqn-21"><mml:msub><mml:mi>P</mml:mi><mml:mrow><mml:mi>e</mml:mi></mml:mrow></mml:msub></mml:math></inline-formula> is calculated based on the relative probabilities of each category being assigned by the raters. Cohen&#x2019;s Kappa commonly falls within the range of [0, 1], such that a value close to 1 is preferable, denoting perfect agreement between raters.</p>
<p>The Dice Coefficient, or Sorensen-Dice Index, is a statistical metric used to evaluate the similarity between two sets. It is widely used in image analysis and medical imaging to assess the accuracy of image segmentation and classification. The Dice Coefficient ranges from 0 to 1, where 0 signifies no overlap between the sets, and 1 denotes perfect overlap. The formula for the Dice Coefficient is shown in <xref ref-type="disp-formula" rid="eqn-17">Eq. (17)</xref>.
<disp-formula id="eqn-17"><label>(17)</label><mml:math id="mml-eqn-17" display="block"><mml:mi>D</mml:mi><mml:mi>i</mml:mi><mml:mi>c</mml:mi><mml:mi>e</mml:mi><mml:mspace width="thinmathspace" /><mml:mi>C</mml:mi><mml:mi>o</mml:mi><mml:mi>e</mml:mi><mml:mi>f</mml:mi><mml:mi>f</mml:mi><mml:mi>i</mml:mi><mml:mi>c</mml:mi><mml:mi>i</mml:mi><mml:mi>e</mml:mi><mml:mi>n</mml:mi><mml:mi>t</mml:mi><mml:mo>=</mml:mo><mml:mfrac><mml:mrow><mml:mn>2</mml:mn><mml:mrow><mml:mo stretchy="false">|</mml:mo></mml:mrow><mml:mi>A</mml:mi><mml:mo>&#x2229;</mml:mo><mml:mi>B</mml:mi><mml:mrow><mml:mo stretchy="false">|</mml:mo></mml:mrow></mml:mrow><mml:mrow><mml:mrow><mml:mo>|</mml:mo><mml:mi>A</mml:mi><mml:mo>|</mml:mo></mml:mrow><mml:mo>+</mml:mo><mml:mrow><mml:mo stretchy="false">|</mml:mo></mml:mrow><mml:mi>B</mml:mi><mml:mrow><mml:mo stretchy="false">|</mml:mo></mml:mrow></mml:mrow></mml:mfrac></mml:math></disp-formula>where <italic>A</italic> denotes the set of predicted positive samples; <italic>B</italic> denotes the set of ground truth positive samples; <inline-formula id="ieqn-22"><mml:math id="mml-ieqn-22"><mml:mrow><mml:mo>|</mml:mo><mml:mi>A</mml:mi><mml:mo>|</mml:mo></mml:mrow></mml:math></inline-formula> denotes the number of elements (or pixels) in set <italic>A</italic>; <inline-formula id="ieqn-23"><mml:math id="mml-ieqn-23"><mml:mrow><mml:mo>|</mml:mo><mml:mi>B</mml:mi><mml:mo>|</mml:mo></mml:mrow></mml:math></inline-formula> denotes the number of elements (or pixels) in set <italic>B</italic>; and <inline-formula id="ieqn-24"><mml:math id="mml-ieqn-24"><mml:mrow><mml:mo stretchy="false">|</mml:mo></mml:mrow><mml:mi>A</mml:mi><mml:mo>&#x2229;</mml:mo><mml:mi>B</mml:mi><mml:mrow><mml:mo stretchy="false">|</mml:mo></mml:mrow></mml:math></inline-formula> denotes the number of elements (or pixels) that are common to both sets <italic>A</italic> and <italic>B</italic>.</p>
<p>Fr&#x00E9;chet Inception Distance (FID) is a metric used to assess the quality of images produced by generative models, such as GANs. It calculates the distance between the distributions of real and generated images in a feature space, which is derived from a pre-trained Inception network, a specific type of convolutional neural network. The FID score evaluates both the quality and diversity of the generated images, making it a commonly used metric for evaluating generative models. The formula for FID is shown in <xref ref-type="disp-formula" rid="eqn-18">Eq. (18)</xref>.
<disp-formula id="eqn-18"><label>(18)</label><mml:math id="mml-eqn-18" display="block"><mml:mi>F</mml:mi><mml:mi>I</mml:mi><mml:mi>D</mml:mi><mml:mo>=</mml:mo><mml:msup><mml:mrow><mml:mo symmetric="true">&#x2016;</mml:mo><mml:msub><mml:mi>&#x03BC;</mml:mi><mml:mrow><mml:mi>r</mml:mi></mml:mrow></mml:msub><mml:mo>&#x2212;</mml:mo><mml:msub><mml:mi>&#x03BC;</mml:mi><mml:mrow><mml:mi>g</mml:mi></mml:mrow></mml:msub><mml:mo symmetric="true">&#x2016;</mml:mo></mml:mrow><mml:mrow><mml:mn>2</mml:mn></mml:mrow></mml:msup><mml:mo>+</mml:mo><mml:mi>T</mml:mi><mml:mi>r</mml:mi><mml:mo stretchy="false">(</mml:mo><mml:msub><mml:mi mathvariant="normal">&#x03A3;</mml:mi><mml:mrow><mml:mi>r</mml:mi></mml:mrow></mml:msub><mml:mo>+</mml:mo><mml:msub><mml:mi mathvariant="normal">&#x03A3;</mml:mi><mml:mrow><mml:mi>g</mml:mi></mml:mrow></mml:msub><mml:mo>&#x2212;</mml:mo><mml:mn>2</mml:mn><mml:mo stretchy="false">(</mml:mo><mml:mrow><mml:msub><mml:mi mathvariant="normal">&#x03A3;</mml:mi><mml:mrow><mml:mi>r</mml:mi></mml:mrow></mml:msub></mml:mrow><mml:mrow><mml:msub><mml:mi mathvariant="normal">&#x03A3;</mml:mi><mml:mrow><mml:mi>g</mml:mi></mml:mrow></mml:msub></mml:mrow><mml:msup><mml:mo stretchy="false">)</mml:mo><mml:mrow><mml:mn>1</mml:mn><mml:mrow><mml:mo>/</mml:mo></mml:mrow><mml:mn>2</mml:mn></mml:mrow></mml:msup><mml:mo stretchy="false">)</mml:mo></mml:math></disp-formula>where <inline-formula id="ieqn-25"><mml:math id="mml-ieqn-25"><mml:msub><mml:mi>&#x03BC;</mml:mi><mml:mrow><mml:mi>r</mml:mi></mml:mrow></mml:msub></mml:math></inline-formula> and <inline-formula id="ieqn-26"><mml:math id="mml-ieqn-26"><mml:msub><mml:mi>&#x03BC;</mml:mi><mml:mrow><mml:mi>g</mml:mi></mml:mrow></mml:msub></mml:math></inline-formula> denote the mean vectors of the features extracted from the real images and generated images, respectively; <inline-formula id="ieqn-27"><mml:math id="mml-ieqn-27"><mml:msub><mml:mi mathvariant="normal">&#x03A3;</mml:mi><mml:mrow><mml:mi>r</mml:mi></mml:mrow></mml:msub></mml:math></inline-formula> and <inline-formula id="ieqn-28"><mml:math id="mml-ieqn-28"><mml:msub><mml:mi mathvariant="normal">&#x03A3;</mml:mi><mml:mrow><mml:mi>g</mml:mi></mml:mrow></mml:msub></mml:math></inline-formula> denote the covariance matrices of the feature representations for the real and generated images, respectively; Tr denotes the trace of a matrix, which is the sum of the diagonal elements. The FID score can be ranged from 0 to infinity, where lower values indicate better performance. A score of 0 means that the generated images perfectly match the real images in the feature space. It is important to remark that the FID is sensitive to both the quality of generated images and the respective diversity. The FID can effectively capture mode collapse scenarios, where a model generates limited variations of images, leading to a higher FID score.</p>
</sec>
</sec>
<sec id="s4">
<label>4</label>
<title>Results</title>
<sec id="s4_1">
<label>4.1</label>
<title>Classification of the Articles in Terms of Generic Categories</title>
<p>Based on <xref ref-type="fig" rid="fig-4">Fig. 4</xref>, the search string, as formalized in <xref ref-type="table" rid="table-2">Table 2</xref>, resulted in 31 included articles. These articles were then characterized into two generic categories, namely diagnosis and treatment. Notice that one included article reported findings using GAI in both the categories. Henceforth, a new category, namely Diagnosis &#x0026; Treatment (i.e., hybrid category) is created. <xref ref-type="fig" rid="fig-5">Fig. 5</xref> shows the classification of the 31 included articles. According to <xref ref-type="fig" rid="fig-5">Fig. 5</xref>, the diagnosis category formalized the main body of the literature, accounting for 90.3% (28 articles) of the included articles. This is followed by articles in treatment and hybrid categories, respectively accounted for 6.5% (2 articles) and 3.2% (1 article). This could be attributed to the superiority of GAI in accomplishing task-specific events [<xref ref-type="bibr" rid="ref-8">8</xref>], for example, data generation and augmentation [<xref ref-type="bibr" rid="ref-22">22</xref>], abnormalities detection [<xref ref-type="bibr" rid="ref-51">51</xref>,<xref ref-type="bibr" rid="ref-52">52</xref>], image-to-image translation [<xref ref-type="bibr" rid="ref-53">53</xref>,<xref ref-type="bibr" rid="ref-54">54</xref>], which formalized the core foundation in computer-aided diagnostics.</p>
<fig id="fig-5">
<label>Figure 5</label>
<caption>
<title>Analysis on the generic categories</title>
</caption>
<graphic mimetype="image" mime-subtype="tif" xlink:href="CMC_63407-fig-5.tif"/>
</fig>
<p>In the treatment domain, personalized regimens may be required most of the time. The capability of GAI in the detection of non-clinical significance can result in overtreatment [<xref ref-type="bibr" rid="ref-12">12</xref>], subsequently leading to unnecessary clinical procedures and associated to morbidity [<xref ref-type="bibr" rid="ref-55">55</xref>], leading to lower interest in using GAI for breast cancer treatment purposes. <xref ref-type="table" rid="table-6">Table A1</xref> in <xref ref-type="sec" rid="app-2">Appendix B</xref> summarizes the details of the 31 included articles, comprised of useful information, for example, the generic category, modalities, dataset, methods, and core findings.</p>

</sec>
<sec id="s4_2">
<label>4.2</label>
<title>Geographical Scientometric Analysis</title>
<p><xref ref-type="fig" rid="fig-6">Fig. 6</xref> shows the geographical scientometric analysis of the included articles. The geographical distribution of the contributing organizations in GAI in breast cancer research demonstrates a wide global engagement, with notable concentrations in certain regions. The USA leads with 8 contributions, highlighting its dominant role in AI-driven breast cancer research. China and India each follow with 4 contributions, indicating strong research activity in Asia. Other Asian countries such as Japan and Korea also show significant participation, with 3 and 2 contributions, respectively. European countries like Germany, Spain, Switzerland, and France collectively contribute 7 works, showcasing the region&#x2019;s involvement in integrating AI with medical research. While Australia, Bangladesh, and the Netherlands each contribute 1 study, this distribution indicates active participation from both developed and developing nations. This wide geographical spread underscore the global importance and collaboration in leveraging AI for breast cancer diagnosis and treatment across diverse healthcare systems. To better illustrate the collaboration between different countries, a co-country-ship network analysis is generated, as in <xref ref-type="fig" rid="fig-7">Fig. 7</xref>. Because of small number of included articles in this study, the co-country-ship network may look scatted. The network provided however remain valid in illustrating the collaborative relationship between the countries as aforementioned. The network reveals three distinct clusters, dominated by the USA, China, and Italy, with the USA at the core of the contributions. This is followed by China, establishing a close network with the United Kingdom. The third cluster features Italy, collaborating with Switzerland, forming the third strong partnership in the network.</p>
<fig id="fig-6">
<label>Figure 6</label>
<caption>
<title>Geographical scientometric analysis of the included review works</title>
</caption>
<graphic mimetype="image" mime-subtype="tif" xlink:href="CMC_63407-fig-6.tif"/>
</fig><fig id="fig-7">
<label>Figure 7</label>
<caption>
<title>Co-country-ship network analysis</title>
</caption>
<graphic mimetype="image" mime-subtype="tif" xlink:href="CMC_63407-fig-7.tif"/>
</fig>
</sec>
<sec id="s4_3">
<label>4.3</label>
<title>Distribution of the Most Contributing Journals</title>
<p><xref ref-type="fig" rid="fig-8">Fig. 8</xref> shows the most contributing journals in reporting findings using GAI in breast cancer. Overall, a total of 29 journals were collated from the 31 included articles. Based on <xref ref-type="fig" rid="fig-8">Fig. 8</xref>, insufficient evidences were found to substantiate or to support the argument on the most contributing journals herein. This is because the distribution of journals is found relatively scarce corresponding to the entire body of the literature. From the collected data, the journal, namely <italic>Journal of Medical Imaging</italic> and <italic>Dignostics</italic>, both ranked as the most contributing journals, but accounted only 6.5% (two articles), respectively, from the included articles. The scattered distribution may be due to the broad applicability of &#x201C;diagnosis,&#x201D; which aligns with the aims and scopes of various journals, for example, those shown in <xref ref-type="fig" rid="fig-8">Fig. 8</xref>. It is important to note that diagnosis in breast cancer occurs at multiple stages, for example, during the examination phase using mammograms or during grading using histopathology images. These diverse diagnostic processes fit within the scope of numerous journals, leading to their widespread inclusion.</p>
<fig id="fig-8">
<label>Figure 8</label>
<caption>
<title>Analysis of most contributing journals</title>
</caption>
<graphic mimetype="image" mime-subtype="tif" xlink:href="CMC_63407-fig-8.tif"/>
</fig>
</sec>
<sec id="s4_4">
<label>4.4</label>
<title>Distribution of the Most Contributing Publishers</title>
<p>As mentioned in <xref ref-type="sec" rid="s3_1">Section 3.1</xref>, general databases, for example, Scopus, Web of Science Core Collection, and PubMed, were used for the literature search process. From all the included articles, 14 publishers were retrieved, such that the top five most contributing publishers are Springer, Elsevier, MDPI, SPIE, and Wolters Kluwer. <xref ref-type="fig" rid="fig-9">Fig. 9</xref> summarises the contributing publishers retrieved from the included articles. From the figure, Springer appeared to be the most contributing publisher, accounted 22.6% (7 articles) in total. This is followed by Elsevier (19.3%, 6 articles), MDPI (12.9%, 4 articles), SPIE (9.6%, 3 articles), and Wolters Kluwer (6.5%, 2 articles). In general, publishers maintain an oligopolistic hold on the publishing industry, a trend consistent with previous findings from an analysis spanning four decades (1973&#x2013;2013). This analysis identified Elsevier, Taylor &#x0026; Francis, and Springer as leading publishers across various topics. The same trend as well can be observed from some of the recent reviews in various fields, for example, agriculture, engineering, applied mathematics, and medicine. The oligopolistic structure of the publishing industry is likely to persist, as building a reputable publishing company requires significant time and resources. Furthermore, researchers may hesitate to submit their work to newer publishers to avoid the risks associated with potential predatory publishers.</p>
<fig id="fig-9">
<label>Figure 9</label>
<caption>
<title>Analysis of most contributing publishers</title>
</caption>
<graphic mimetype="image" mime-subtype="tif" xlink:href="CMC_63407-fig-9.tif"/>
</fig>
</sec>
<sec id="s4_5">
<label>4.5</label>
<title>Temporal Scientometric Analysis</title>
<p><xref ref-type="fig" rid="fig-10">Fig. 10</xref> shows the temporal scientometric analysis for the included articles. In order to maximize the data retrieved pertaining to the proposed search string, no limiter is implemented on the publication year. Based on the figure, the temporal distribution demonstrates a continual increment in the topic of interest, with the first relevant publication in the year 2007. Relevant publication in GAI, specifically in breast cancer was not evident from the years 2008 to 2015, with limited growth observed. This slow start can be attributed to the early stage of AI development, where machine learning and AI applications in healthcare were still nascent, and there was limited access to large datasets, computing power, and expertise. However, from 2018 to 2022, there was a gradual increase in publications, reflecting the rise of deep learning techniques, particularly with the introduction of GAI in 2014. These advancements allowed for greater exploration in medical imaging, including tasks like cancer diagnosis, image segmentation, and data augmentation. The availability of better computational resources, such as GPUs, and the development of pre-trained models further fueled research efforts, leading to an increase in publications. The most significant surge occurred in 2023 and 2024, with the number of publications rising sharply to 11 and 9, respectively. This dramatic increase is likely due to the growing adoption of advanced generative AI models, such as YOLO and transformer-based architectures, which have proven highly effective in medical imaging applications. Researchers are increasingly recognizing the potential of AI in enhancing breast cancer diagnosis, classification, and even generating synthetic datasets for training purposes. This surge also reflects the broader trend of AI integration in healthcare, as interdisciplinary collaborations between AI researchers and medical professionals become more common, leading to more impactful studies and publications. Overall, the trend indicates that GAI&#x2019;s role in breast cancer research is rapidly expanding, with further growth expected as AI technologies continue to evolve and find new applications in the medical field.</p>
<fig id="fig-10">
<label>Figure 10</label>
<caption>
<title>Temporal scientometric analysis of the included review works</title>
</caption>
<graphic mimetype="image" mime-subtype="tif" xlink:href="CMC_63407-fig-10.tif"/>
</fig>
</sec>
<sec id="s4_6">
<label>4.6</label>
<title>Subject Areas Profiling</title>
<p><xref ref-type="fig" rid="fig-11">Fig. 11</xref> shows the subject areas profiling retrieved from the included articles in this study. Based on the figure, the subject area profiling for the 31 included works in GAI applied to breast cancer reveals a multidisciplinary research trend. Medicine is as the most dominant field, particularly in Radiology, Nuclear Medicine, and Imaging. This is then followed by Oncology, a sub-field of Medicine, reflecting the critical role of AI in medical imaging and cancer diagnosis. The presence of Computer Science areas, for example, AI Applications, Computer Vision, and Pattern Recognition highlights the use of computational methods in image analysis and diagnostics. Engineering fields, for example, Biomedical Engineering and Electrical Engineering underscore the integration of technology for enhanced healthcare solutions. Biochemistry, Genetics, and Molecular Biology, with emphasis on Cancer Research, and Materials Science also play crucial roles, pointing to advancements in the understanding and treatment of breast cancer through biomaterials and molecular studies. This multidisciplinary approach showcases the convergence of medicine, computer science, and engineering in leveraging AI to improve breast cancer diagnosis and treatment.</p>
<fig id="fig-11">
<label>Figure 11</label>
<caption>
<title>Subject area profiling</title>
</caption>
<graphic mimetype="image" mime-subtype="tif" xlink:href="CMC_63407-fig-11.tif"/>
</fig>
</sec>
<sec id="s4_7">
<label>4.7</label>
<title>Keywords Co-Occurrence Mapping</title>
<p><xref ref-type="fig" rid="fig-12">Fig. 12</xref> shows the thematic landscape of the included articles, focusing on GAI in breast cancer. The co-occurrence mapping of keywords reveals three distinct clusters, categorized by objects of interest, methodologies, and relevant sub-field approaches. The objects of interest cluster appear to be the most prominent cluster, indicated by the prevalence of keywords, for example, &#x201C;breast,&#x201D; &#x201C;breast neoplasms,&#x201D; and &#x201C;breast tumour.&#x201D; This is followed by the methodology cluster, characterized by keywords, for example, &#x201C;artificial intelligence&#x201D; and &#x201C;controlled study.&#x201D; The third cluster comprises keywords, for example, &#x201C;image processing&#x201D; and &#x201C;machine learning&#x201D;. Notably, the keyword &#x201C;artificial intelligence&#x201D; appears as the largest dot on the map, highlighting its widespread adoption across the included articles. This prominence is justifiable, given the literature search focuses on GAI in breast cancer. Additionally, the sub-field approaches, including &#x201C;deep learning&#x201D;, &#x201C;generative adversarial networks&#x201D;, and advancements in algorithms, signify significant innovations within the realm of artificial intelligence. From the perspective of objects of interest, the mapping indicates that topics such as &#x201C;diagnostic imaging&#x201D;, &#x201C;mammography&#x201D;, &#x201C;breast neoplasms&#x201D;, and &#x201C;breast tumours&#x201D; have garnered considerable attention from researchers over the past decades.</p>
<fig id="fig-12">
<label>Figure 12</label>
<caption>
<title>Keywords co-occurrence mapping</title>
</caption>
<graphic mimetype="image" mime-subtype="tif" xlink:href="CMC_63407-fig-12.tif"/>
</fig>
</sec>
</sec>
<sec id="s5">
<label>5</label>
<title>Self-Assessment, Limitations, Challenges, and Future Direction</title>
<sec id="s5_1">
<label>5.1</label>
<title>Self-Assessment</title>
<p>The present study is a systematic review that focuses on the diagnosis and treatment of breast cancer. To maximize the data retrieved, no limiter is set on publication years. Here, a structured review methodology was used to collate, analyze, and synthesize the findings, highlighting patterns, trends, and the contents of included works in the topic of interest. A structured search strategy was proposed in compliance with the PRISMA guideline as detailed in <xref ref-type="sec" rid="s3_2">Section 3.2</xref>. To affirm the quality of this study, an appraisal tool, namely A Measurement Tool to Assess Systematic Review (AMSTAR) is used to assess the quality of the present study in view of the content validity (see <xref ref-type="table" rid="table-5">Table 5</xref>). AMSTAR is a self-appraisal tool that is commonly used to assess the quality of a systematic review, specifically to determine if the systematic reviews are comprehensive, have proper referencing, and are equipped with added value to the readers. The AMSTAR comprises 11 components for content validity. According to <xref ref-type="table" rid="table-5">Table 5</xref>, the present study obtained one &#x201C;no&#x201D;, 10 &#x201C;yes&#x201D;, and one &#x201C;NA&#x201D;. Justifications were provided for each component to better support the evaluation outputs, as recommended by [<xref ref-type="bibr" rid="ref-8">8</xref>].</p>
<table-wrap id="table-5">
<label>Table 5</label>
<caption>
<title>Quality assessment on this study using AMSTAR appraisal tool. Note: &#x002B;, &#x2212;, and NA denote yes, no, and not applicable, respectively</title>
</caption>
<table>
<colgroup>
<col align="center"/>
<col align="center"/>
<col align="center"/>
<col align="center"/>
</colgroup>
<thead>
<tr align="center">
<th>Item</th>
<th>Description</th>
<th>Rating</th>
<th>Justification</th>
</tr>
</thead>
<tbody>
<tr align="center">
<td>1</td>
<td>Was an &#x2018;a priori&#x2019; design provided?</td>
<td>&#x002B;</td>
<td>Yes, the eligible criteria are provided in <xref ref-type="sec" rid="s3_2">Section 3.2</xref></td>
</tr>
<tr align="center">
<td>2</td>
<td>Was there duplicate study selection and data extraction?</td>
<td>&#x002B;</td>
<td>Yes, excluded as detailed in <xref ref-type="fig" rid="fig-2">Fig. 2</xref></td>
</tr>
<tr align="center">
<td>3</td>
<td>Was a comprehensive literature search performed?</td>
<td>&#x002B;</td>
<td>Yes, as detailed in <xref ref-type="sec" rid="s3_1">Section 3.1</xref></td>
</tr>
<tr align="center">
<td>4</td>
<td>Was the status of publication (i.e., grey literature) used as an inclusion criterion?</td>
<td>&#x2013;</td>
<td>No, inclusion criteria are provided in <xref ref-type="sec" rid="s3_2_1">Section 3.2.1</xref></td>
</tr>
<tr align="center">
<td>5</td>
<td>Was a list of studies (included and excluded) provided?</td>
<td>&#x002B;</td>
<td>Yes, provided in <xref ref-type="sec" rid="app-2">Appendix B</xref></td>
</tr>
<tr align="center">
<td>6</td>
<td>Were the characteristics of the included studies provided?</td>
<td>&#x002B;</td>
<td>Yes, provided in <xref ref-type="sec" rid="app-2">Appendix B</xref></td>
</tr>
<tr align="center">
<td>7</td>
<td>Was the scientific quality of the included studies assessed and documented?</td>
<td>NA</td>
<td>NA</td>
</tr>
<tr align="center">
<td>8</td>
<td>Was the scientific quality of the included studies used appropriately in formulating conclusions?</td>
<td>&#x002B;</td>
<td>Yes, the scientific quality of the included review works from different perspectives were considered (<xref ref-type="sec" rid="s4">Section 4</xref>). Challenges in GAI adoption in clinical settings are provided in <xref ref-type="sec" rid="s5_3">Section 5.3</xref></td>
</tr>
<tr align="center">
<td>9</td>
<td>Were the methods used to combine the findings of studies appropriate?</td>
<td>&#x002B;</td>
<td>Yes, as detailed in <xref ref-type="sec" rid="s3_3">Sections 3.3</xref> and <xref ref-type="sec" rid="s3_4">3.4</xref></td>
</tr>
<tr align="center">
<td>10</td>
<td>Was the likelihood of publication bias assessed?</td>
<td>&#x002B;</td>
<td>Yes, as detailed in <xref ref-type="sec" rid="s5_2">Sections 5.2</xref></td>
</tr>
<tr align="center">
<td>11</td>
<td>Was the conflict of interest stated?</td>
<td>&#x002B;</td>
<td>Yes, as detailed in the Conflicts of Interest Section</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
<sec id="s5_2">
<label>5.2</label>
<title>Limitations</title>
<p>The findings of this study are subjected to several limitations. First, only full-text articles available in the English language are included in the synthesis process in accordance with the PRISMA guideline. Non-English material and/or articles without full text would be excluded in Phase 1 of the exclusion criteria. This may potentially introduce bias into the analysis, affecting the description of patterns and trends of the included articles in the topic of interest. Second, based on the proposed search string (<xref ref-type="table" rid="table-2">Table 2</xref>), only articles utilizing GAI in breast cancer are retrieved. Therefore, emerging GAI models that are reported in other cancer types that potentially offer useful insight and utility in breast cancer may be excluded. Third, articles that were not indexed and populated by Scopus, Web of Science Core Collection, and PubMed databases were not included in the synthesis process. Lastly, grey literature is not included in the synthesis activities. This is mainly because the grey literature may lack rigorous peer review, subsequently resulting in inconsistent quality, associated with risk of bias, and challenging for reproducibility. However, considering the diversity and structured search methodology (in compliance with the PRISMA guideline) adopted here in retrieving articles within the topic of interest, the present study is confident with the findings synthesized from the included articles, such that the majority of the relevant literature has been included, and the findings accurately represent the current state of research.</p>

</sec>
<sec id="s5_3">
<label>5.3</label>
<title>Challenges in GAI Adoption in Clinical Settings</title>
<p>While recognizing GAI as the potential game-changer to meet the ever-increasing demand for quality healthcare in breast cancer, typically in the era of precision medicine, the technology is inevitable to inherit challenges in various spectrums for widespread clinical adoption. Awareness of the constraints of the current GAI-based systems and concerted efforts (from researchers and industry experts) are essential in pushing GAI technology to impact the future direction of breast cancer research.</p>
<p>Similar to all the discriminative models, the nature of data-driven in GAI-based systems is inevitable to bias [<xref ref-type="bibr" rid="ref-56">56</xref>,<xref ref-type="bibr" rid="ref-57">57</xref>], as this serves as the foundation for the generative models. Here, two biases are identified: data bias and algorithm bias. Data bias could potentially occur in the training phase when the training data comprises information from a specific cohort, while under-represented cohorts may be afflicted by the GAI outputs, assuming the output solutions fulfill the input prompts. For example, a GAI falsely identifies black patients as being healthier than white patients who suffered from the same illness when the cost of healthcare is used as the proxy. This is inaccurate as black patients receive less medical cost attention. Thus, injecting faulty perception into the training data, which subsequently reflects in the output solutions [<xref ref-type="bibr" rid="ref-58">58</xref>]. Likewise, countries with poor data registries, especially low-resource countries, are at risk of being under-represented in GAI-based systems, leading to skewed or inaccurate diagnostic and treatment recommendations [<xref ref-type="bibr" rid="ref-59">59</xref>,<xref ref-type="bibr" rid="ref-60">60</xref>]. If the generative model training data disproportionately reflects healthcare practices and/or patient demographics from high-resource countries, the GAI-based system may fail to adequately address the unique needs and/or health profiles of populations in low-resource regions. This can exacerbate existing healthcare disparities, as the outputs generated by such GAI models might misinterpret conditions prevalent in these under-represented cohorts. Consequently, bias in training data not only compromises the fairness and accuracy of GAI outputs but also raises ethical concerns about its application in global healthcare systems, particularly for vulnerable populations. Algorithm bias or mode collapse is defined as a situation where a GAI fails to capture the full diversity of the training data, resulting in repetitive or limited variations in the generated outputs [<xref ref-type="bibr" rid="ref-61">61</xref>]. Often, this bias originates from overfitting, where the generative models fail to accurately learn the underlying distribution of the training data, producing identical outputs with no variation [<xref ref-type="bibr" rid="ref-62">62</xref>].</p>
<p>Generalization and adaptation of GAI denote the model capability to produce a new and diverse output that is not directly replicated from the training data, implying the superiority of GAI in capturing the underpinning patterns and distributions of the training data and reflected in the output solution [<xref ref-type="bibr" rid="ref-63">63</xref>&#x2013;<xref ref-type="bibr" rid="ref-66">66</xref>]. For example, a robust GAI shall demonstrate promising performance even when the input prompts are pertaining to breast histopathology images that are not presented in the training data. A well-generalized GAI can generate realistic and meaningful data across various scenarios, even when presented with inputs or conditions that have not been explicitly encountered during training. Generalization is crucial to avoid overfitting, ensuring that the model can generalize the patterns (from the training data) and adapt to unseen data while maintaining high performance in real-world applications. Considering the diversity of incoming patients (i.e., wide variety of races, ethnicity, nationality, and dietary backgrounds), GAIs that lack generalization are not reliable, increasing the risk associated, afflicting the diagnostic and treatment recommendations, ultimately, fragmenting the quality of healthcare service and exacerbate trust in GAI for clinical adoption. Adapting the GAI models to a new domain is now an ongoing challenge, where techniques, for example, fine-tuning, domain adaptation, and transfer learning are continued to be explored to address the present challenge.</p>
<p>Because of the generative nature of GAI, the model is susceptible to hallucination or confabulation, where the model itself expects a plausible output solution. In fact, the solution generated is unreasonable with respect to the training data [<xref ref-type="bibr" rid="ref-67">67</xref>,<xref ref-type="bibr" rid="ref-68">68</xref>]. The erroneous and/or misleading output solutions are not a result of bias, but the output solutions are factually incorrect, unrealistic, and/or completely unrelated to the training data. To date, the core reasons underpinning hallucination or confabulation are still mysterious, with early inference that training data embedded with fictional or contradictory content besides factual information may further promote the risk of hallucination [<xref ref-type="bibr" rid="ref-69">69</xref>]. This may suggest the importance of data cleaning (i.e., removal of outliers) in the training phase, to avoid skewed models due to disproportionate influence, distorted learning, and random noise resulting from the outliers. Considering the rich amount of training data in GAI, data cleaning is tedious and cumbersome however, especially for medical experts with mediocre knowledge of computational engineering and data analytics. Concerted efforts in data cleaning, data transparency, and algorithm error-checking mechanisms may be required to mitigate the aforementioned problem.</p>
<p>Transparency, explainability, and interpretability of an AI system in clinical settings are crucial, as medical decisions cannot be adopted solely from a &#x201C;black box&#x201D; model, which lacks sophisticated reasonings and justifications, with output solutions that are challenging to verify [<xref ref-type="bibr" rid="ref-70">70</xref>]. Unlike the discriminative model, the explainable model, for example, Explainable Artificial Intelligence (XAI) [<xref ref-type="bibr" rid="ref-71">71</xref>] in the generative model is still in its infancy with robust models yet to surface. Additionally, a recent study argues that the GAI (i.e., typically LLM) that gained interest across multiple spectrums due to its formal reasoning capabilities, particularly in mathematics may not be accurate. The findings argue the hypothesis with evidence proving the LLMs may not be capable of genuine local reasoning but, in fact, replicating the reasoning steps based on the observation in the training phase [<xref ref-type="bibr" rid="ref-72">72</xref>]. Transparency in GAI holds an important role, especially when multiple output solutions could be produced toward the same input prompts. Thus, sensemaking in fulfilling the input prompts is essential. To date, most of the GAIs are trained on a pre-trained model with respective fine-tuning performed in accordance with different circumstances or applications for local adaptation.</p>
<p>From a regulatory standpoint, the use of GAI-generated medical data introduces complex issues related to data privacy, intellectual property, and legal responsibilities, specifically, in the context of cross-border healthcare collaboration. Data privacy is a primary concern, as aforementioned, the data-driven GAI models often rely on large datasets, which may comprise sensitive patient information. Ensuring compliance with data protection regulations such as the General Data Protection Regulation (GDPR) in the European Union or the Health Insurance Portability and Accountability Act (HIPAA) in the United States becomes challenging in cross-border settings, where differing privacy standards may conflict. Additionally, the origins and handling of data used to train pre-trained models may lack transparency (i.e., black-box), raising ethical concerns about patient consent and data provenance. Intellectual property issues further complicate the landscape, as questions arise over the ownership of GAI-generated content, the rights to the original training data, and liability for errors or misuse of model outputs [<xref ref-type="bibr" rid="ref-73">73</xref>]. Events involving cross-border collaborations further exacerbate the situation, where intellectual property laws vary significantly between countries [<xref ref-type="bibr" rid="ref-74">74</xref>,<xref ref-type="bibr" rid="ref-75">75</xref>]. Legal responsibilities also present challenges, as determining accountability for adverse outcomes or misdiagnoses stemming from GAI-generated recommendations can be difficult, especially when models are developed in one jurisdiction and deployed in another. Differing healthcare regulations and liability frameworks across borders further complicate the establishment of clear accountability. Addressing these issues requires robust international frameworks to harmonize data privacy standards, clarify intellectual property rights, and establish legal accountability, ensuring the ethical and responsible use of GAI in global healthcare collaborations.</p>
<p>The adoption of GAI in clinical settings requires comprehensive technical support, planned preventive maintenance, and robust infrastructure readiness. This includes ensuring the availability of high-performance workstations and sufficient energy supply to handle the intensive computational demands of GAI models. Additionally, having skilled experts on hand is crucial to address daily technical difficulties and to provide manpower for routine maintenance and system checks. Cybersecurity is another critical aspect, as the integrity of GAI models must be safeguarded against potential hacking attempts that could compromise GAI accuracy and reliability [<xref ref-type="bibr" rid="ref-76">76</xref>]. Mitigation measures must also be in place to prevent malicious interference, for example, the introduction of noise or unauthorized alterations to the models, which could jeopardize healthcare services, afflicting the generative recommendations. Ensuring both technical and cybersecurity readiness is key to the safe and effective implementation of GAI in clinical environments. Considering all these requirements, ranging from infrastructure and energy to expert manpower and cybersecurity, the associated cost becomes a significant factor in the adoption process [<xref ref-type="bibr" rid="ref-77">77</xref>]. To keep healthcare affordable, GAI should not solely aim to eliminate occasional errors made by medical experts but should instead focus on fully automating specific procedures currently performed by experts. The primary goal of GAI in breast cancer research shall focus on enhancing clinical efficiency while avoiding unnecessary healthcare costs.</p>
<p>Misuse of GAI is not new, especially in domains involving entertainment and social media using techniques, for example, deepfakes. Considering the ease and robustness of the deepfake techniques in this era, the low cost of implementation, as well as sub-optimal legal boundaries, it is challenging to affirm a GAI is free from malicious actions if a comprehensive adversarial monitoring system is not in place [<xref ref-type="bibr" rid="ref-78">78</xref>]. Factors contributing to misuse of GAI in breast cancer, especially in diagnosis and treatment can be multi-factorial, especially involving enormous personal interests that may arise from conflicts, for example, malicious incidences involving insurance claims and tension between opting for optimal healthcare or medical profit. These underscore the vulnerability of GAI to malicious actions and exploitation, with potential threats that collectively hinder trust in GAI in clinical settings.</p>
<p>While GAI poses significant advancement and revolutionizes breast cancer research, typically in diagnosis and treatment stages, offering enhanced efficiency and productivity in clinical operations, awareness of the challenges of GAI adoption is important. The far-reaching risks of GAI, typically in bias, hallucination or confabulation, and misuse required concerted and sustained efforts from researchers and industry experts in developing comprehensive mitigation mechanisms and solutions to ensure responsible AI usage. The adoption of GAI can be performed in multiple stages, where continuous temporal assessment and quality improvement are implemented at different checkpoints [<xref ref-type="bibr" rid="ref-25">25</xref>], and allows interrogation and feedback from experts at different levels as well as consumers and the public, aiming for robust and reliable GAI adoption.</p>
</sec>
<sec id="s5_4">
<label>5.4</label>
<title>Future Direction</title>
<p>As GAI continues to evolve, its integration into clinical practice requires a multidisciplinary approach, addressing technical, ethical, legal, and practical considerations. Ensuring the successful deployment of GAI in breast cancer diagnosis and treatment will depend on collaborative efforts among researchers, policymakers, healthcare institutions, and clinical practitioners. This section outlines key focus areas and strategies for advancing GAI in healthcare.</p>
<p>From a researcher&#x2019;s standpoint, the primary focus should be on developing GAI models that are robust against bias and capable of generalizing across diverse patient populations. This necessitates the creation of inclusive and representative training datasets, particularly from underrepresented cohorts and low-resource regions. Techniques such as domain adaptation, transfer learning, and federated learning should be explored to ensure GAI models perform reliably across varied demographics and healthcare settings. Additionally, XAI for generative models must be advanced to enhance clinicians&#x2019; trust in GAI-generated outputs. Developing interpretable models that provide clear justifications for their recommendations, along with visualization tools for decision-making processes, will be crucial for bridging the gap between AI and clinical practice. Furthermore, reducing hallucinations in GAI models is essential for improving reliability. This can be achieved through robust data-cleaning pipelines, outlier detection mechanisms, and error-checking algorithms that ensure the accuracy and consistency of generated solutions. Collaboration between AI developers and medical experts is critical to refining these processes and maintaining clinical relevance.</p>
<p>From a policymaker&#x2019;s standpoint, establishing legal and ethical frameworks is essential for facilitating cross-border collaboration in GAI research and deployment. Regional and international alliances are necessary to create standardized regulations for data privacy, intellectual property, and legal accountability, ensuring the global adoption of GAI in healthcare. Open-access initiatives, such as DeepSeek, can serve as models for promoting transparency and equitable access to GAI technologies. Policymakers should also develop guidelines for data sharing, model ownership, and liability, ensuring that GAI systems are deployed responsibly and ethically. Effective collaboration among policymakers, researchers, and industry stakeholders is necessary to establish harmonized frameworks that balance technological innovation with patient rights and ethical considerations.</p>
<p>From a healthcare institution&#x2019;s standpoint, a phased approach to GAI adoption should be considered for seamless integration into clinical workflows. Initially, GAI can be implemented in low-risk applications such as data augmentation, image synthesis, and preliminary diagnostic support, allowing healthcare providers to build confidence in the technology while minimizing risks to patient care. Establishing scalable and secure computational infrastructure is crucial for supporting the demands of GAI in clinical settings. This includes high-performance workstations, energy-efficient systems, and robust cybersecurity measures to protect sensitive patient data and maintain the integrity of GAI models. Additionally, comprehensive training programs and workshops should be provided to clinical practitioners to equip them with the necessary knowledge for effectively utilizing GAI technologies in medical practice.</p>
<p>From a clinical practitioner&#x2019;s standpoint, collaboration with healthcare institutions is crucial in establishing strong data governance frameworks that comply with data privacy regulations such as GDPR and HIPAA. This includes verifying the provenance of training data used in GAI models and obtaining informed patient consent for data usage. Before fully integrating GAI into clinical workflows, clinicians should treat GAI-generated recommendations as supplementary tools, rather than definitive solutions. Rigorous validation of AI-generated outputs against clinical expertise and established guidelines is necessary to ensure patient safety and prevent over-reliance on AI systems. Clinical practitioners also play a vital role in advocating for the ethical use of AI by participating in policy discussions, addressing biases in AI models, and ensuring that GAI technologies prioritize patient welfare and equity. Continuous research and collaboration between clinicians and AI researchers are essential to refine GAI models and ensure their practical applicability in real-world healthcare settings.</p>
<p>Achieving full integration of GAI in clinical practice will require a multidisciplinary effort. Experts from various fields must exchange knowledge, break down research silos, and complement each other&#x2019;s expertise to foster the development of innovative solutions. By addressing the technical, legal, and practical challenges, GAI has the potential to revolutionize breast cancer diagnosis and treatment, ultimately improving patient outcomes and advancing precision medicine.</p>
</sec>
</sec>
<sec id="s6">
<label>6</label>
<title>Conclusion</title>
<p>In this study, a holistic birds-eye view of the research reviewing past literature with GAI in breast cancer is presented. Here, a thorough search string in compliance with the PRISMA guideline is proposed. The findings of the systematic review provide useful insight into the holistic view of how research communities contribute, the primary methods employed, the findings of included works, the publications trend, and the development of collaborative networks over time. Based on the analysis outcomes, this study highlighted: (1) the main research domain in GAI in breast cancer research fall within the diagnosis category, accounting for 90.3% (28 articles) of the included articles; (2) geographical scientometric analysis shows that USA leads the AI-driven breast cancer research with 8 contributions in the body of the literature; (3) the <italic>Journal of Medical Imaging</italic> and <italic>Dignostics</italic> are both ranked as the most contributing journals; (4) the publisher, namely Springer is found to be the most contributing publisher, accounted 22.6% (7 articles) in total; (5) based on the temporal scientometric analysis, from 2018 to 2022, there was a gradual increase in publications with the highest publications of 11 and 9 in 2023 and 2024, respectively; (6) in subject area profiling, the subject area of Medicine appears to be the most dominant field, specifically in Radiology, Nuclear Medicine, and Imaging; and (7) three broad thematic clusters found in keyword co-occurrence analysis, namely objects of interest, methodologies, and relevant sub-field approaches. The systematic review serves as a scientific communication, highlighting the research gap and challenges in the topic of interest. For newcomers to the field, this systematic review offers a comprehensive and timely overview, providing valuable insights into the intellectual landscape, understanding literature development, and outlining the potential challenges. For experienced researchers, it serves as a resource to stay updated, particularly in identifying relevant research areas that extend beyond their primary focus. For stakeholders, this systematic review can help prioritize research and funding to support impactful and urgent solutions through GAI integration in breast cancer research, typically in supporting diagnosis and treatment purposes.</p>
</sec>
</body>
<back>
<ack>
<p>The authors are grateful to all the editors and anonymous reviewers for their comments and suggestions.</p>
</ack>
<sec>
<title>Funding Statement</title>
<p>This study received financial support from the Fundamental Research Grant Scheme (FRGS) under grant number: FRGS/1/2024/ICT02/TARUMT/02/1, from the Ministry of Higher Education Malaysia. The Article Processing Charge (APC) was funded in part by the internal grant from the Tunku Abdul Rahman University of Management and Technology (TAR UMT) with grant number: UC/I/G2024-00129.</p>
</sec>
<sec>
<title>Author Contributions</title>
<p>Concept and design: Xiao Jian Tan, Wai Loon Cheor, and Khairul Shakir Ab Rahman. Acquisition of data: Xiao Jian Tan and Wai Loon Cheor. Analysis and interpretation of data: Xiao Jian Tan, Ee Meng Cheng, and Chee Chin Lim. Drafting the manuscript: Xiao Jian Tan. Statistical analysis: Xiao Jian Tan and Wai Loon Cheor. All authors reviewed the results and approved the final version of the manuscript.</p>
</sec>
<sec sec-type="data-availability">
<title>Availability of Data and Materials</title>
<p>Not applicable.</p>
</sec>
<sec>
<title>Ethics Approval</title>
<p>Not applicable.</p>
</sec>
<sec sec-type="COI-statement">
<title>Conflicts of Interest</title>
<p>The authors declare no conflicts of interest to report regarding the present study.</p>
</sec>
<app-group id="apg-1">
<app id="app-1">
<title>Appendix A</title>
<fig id="fig-13">
<label>Figure A1</label>
<caption>
<title>Brief timeline of AI advancement. Note: SHRDLU is an early natural-language understanding computer program</title>
</caption>
<graphic mimetype="image" mime-subtype="tif" xlink:href="CMC_63407-fig-13.tif"/>
</fig>
</app>
<app id="app-2"><title>Appendix B</title>
<table-wrap id="table-6">
<label>Table A1</label>
<caption>
<title>Summary of the included articles</title>
</caption>
<table>
<colgroup>
<col align="center"/>
<col align="center"/>
<col align="center"/>
<col align="center"/>
<col align="center"/>
<col align="center"/>
<col align="center"/>
</colgroup>
<thead>
<tr align="center">
<th align="center">Reference</th>
<th align="center">Year</th>
<th align="center">Category</th>
<th align="center">Modalities</th>
<th align="center">Dataset</th>
<th align="center">Methods</th>
<th align="center">Findings</th>
</tr>
</thead>
<tbody>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-79">79</xref>]</td>
<td>2024</td>
<td>Diagnosis</td>
<td>MRI</td>
<td>Custom</td>
<td>Diffusion probabilistic models (DDPM) and generative adversarial networks (GAN)</td>
<td><list list-type="order">
<list-item>
<p>The GAN-generated images were favored by both radiologists at the 5% dose level.</p></list-item>
<list-item>
<p>At the 25% dose level, both radiologists showed a preference for the DDPM-generated images.</p></list-item>
<list-item>
<p>Both GAN and DDPM demonstrated encouraging performance in reconstructing low-dose images.</p></list-item>
<list-item>
<p>Neither model consistently outperformed the other across all dose levels and evaluation metrics.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-21">21</xref>]</td>
<td>2024</td>
<td>Diagnosis</td>
<td>Mammogram</td>
<td>Custom</td>
<td>Cycle-GAN based Lesion Remover</td>
<td><list list-type="order">
<list-item>
<p>The integrated model combining all networks achieved AUC values between 0.963 and 0.974 for distinguishing images containing recalled lesions from those of normal breast tissue.</p></list-item>
<list-item>
<p>A significant improvement was observed (<italic>p</italic>-value &#x003C; 0.001) compared to the baseline models, with AUCs ranging from 0.914 to 0.967.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-25">25</xref>]</td>
<td>2024</td>
<td>Diagnosis</td>
<td>NA</td>
<td>NA</td>
<td>ChatGPT version 3.5 (ChatGPT3.5)</td>
<td><list list-type="order">
<list-item>
<p>In this experiment, ChatGPT should not be regarded as a dependable resource for radiation oncology information, either for patients or healthcare providers, as it often produces inaccurate or incomplete responses.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-80">80</xref>]</td>
<td>2024</td>
<td>Diagnosis</td>
<td>Histopathology</td>
<td>Custom</td>
<td>High-resolution prediction network (HRPN)</td>
<td><list list-type="order">
<list-item>
<p>The proposed method demonstrates low error rates (mean squared error &#x003D; 1.434, root mean squared error &#x003D; 1.198), a high goodness of fit (R&#x00B2; &#x003D; 0.891), and enhanced image quality (peak signal-to-noise ratio &#x003D; 44.548) compared to a model based on a generative adversarial network structure.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-51">51</xref>]</td>
<td>2024</td>
<td>Diagnosis</td>
<td>Ultrasonography</td>
<td>Kaggle database</td>
<td>Multi Disease Visual Attention Condenser Network (MD-VACNet)</td>
<td><list list-type="order">
<list-item>
<p>The model achieved promising results in classifying breast cancer as benign or malignant, with accuracy, sensitivity, and specificity scores of 98.47%, 98.42%, and 98.31%, respectively.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-81">81</xref>]</td>
<td>2024</td>
<td>Treatment</td>
<td>NA</td>
<td>NA</td>
<td>Generative pre-trained transformer 4 (GPT-4)</td>
<td><list list-type="order">
<list-item>
<p>In this experiment, GPT-4 was unable to recommend initial medication dosages in response to the first prompt and failed to offer a more compassionate, non-pharmacological approach to managing anorexia, even after receiving a follow-up prompt.</p></list-item>
<list-item>
<p>GPT-4 could serve as a preliminary screening tool by offering basic management suggestions, which should be reviewed and validated by healthcare professionals prior to any formal consultation.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-56">56</xref>]</td>
<td>2024</td>
<td>Diagnosis; Treatment</td>
<td>NA</td>
<td>NA</td>
<td>Large language models (LLMs)</td>
<td><list list-type="order">
<list-item><p>Radiologists aiming to enhance productivity should become acquainted with modern large language models (LLMs) and their various versions.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-53">53</xref>]</td>
<td>2024</td>
<td>Diagnosis</td>
<td>Ultrasonography</td>
<td>Custom</td>
<td>Deep convolutional GAN (DCGAN) image</td>
<td><list list-type="order">
<list-item>
<p>The diagnostic accuracy from synthetic images was 86.0% for Reader 1 and 78.0% for Reader 2, compared to 88.0% and 78.0%, respectively, when using original images.</p></list-item>
<list-item>
<p>The kappa coefficients were 0.625 for synthetic images and 0.650 for original images.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-26">26</xref>]</td>
<td>2024</td>
<td>Diagnosis</td>
<td>NA</td>
<td>NA</td>
<td>Chat generative pretrained transformer (ChatGPT) and Bing AI</td>
<td><list list-type="order">
<list-item>
<p>Out of the 117 questions assessed, ChatGPT and Bing achieved average scores of 3.9 and 3.2, respectively (<italic>p</italic> &#x003C; 0.001), with corresponding overall DISCERN scores of 4.1 and 4.4.</p></list-item>
<list-item>
<p>When analyzed by disease type, ChatGPT and Bing scored 3.9 and 3.6 for prostate cancer (<italic>p</italic> &#x003D; 0.02), 3.7 and 3.3 for lung cancer (<italic>p</italic> &#x003C; 0.001), 4.1 and 2.9 for breast cancer (<italic>p</italic> &#x003C; 0.001), and 3.8 and 3.0 for colorectal cancer (<italic>p</italic> &#x003C; 0.001).</p></list-item>
<list-item>
<p>Based on question type, the average scores for ChatGPT and Bing were 3.6 and 3.4 for prognostic questions (<italic>p</italic> &#x003D; 0.12), 3.9 and 3.1 for treatment-related questions (<italic>p</italic> &#x003C; 0.001), and 4.2 and 3.3 for miscellaneous queries (<italic>p</italic> &#x003D; 0.001).</p></list-item>
<list-item>
<p>At least one panelist identified serious or significant flaws in 3% of ChatGPT&#x2019;s responses and 15% of Bing&#x2019;s responses.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-28">28</xref>]</td>
<td>2023</td>
<td>Treatment</td>
<td>NA</td>
<td>NA</td>
<td>Virtual Screening with Generative Neural Network (GNN) via MolAICal (ZINCMol) software</td>
<td><list list-type="order">
<list-item>
<p>The research investigated a systematic approach for accurately determining a drug&#x2019;s structure and validated the method through the results obtained.</p></list-item>
<list-item>
<p>This lays the groundwork for experimentally synthesizing the inhibitor and conducting <italic>in-vitro</italic> and <italic>in-vivo</italic> studies against the MCF7 breast cancer cell line.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-54">54</xref>]</td>
<td>2023</td>
<td>Diagnosis</td>
<td>Mammogram</td>
<td>INbreast,81 OPTIMAM,82 BCDR,83 CBIS-DDSM,86 and CSAW.88</td>
<td>Medigan, a comprehensive platform for pretrained generative models, implemented as an open-source, framework-independent Python library</td>
<td><list list-type="order">
<list-item>
<p>The study of Medigan was conducted across three areas: (a) facilitating community-wide sharing of restricted data, (b) exploring evaluation metrics for generative models, and (c) enhancing clinical downstream tasks.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-82">82</xref>]</td>
<td>2023</td>
<td>Diagnosis</td>
<td>NA</td>
<td>NA</td>
<td>LLM ChatGPT 3.5</td>
<td><list list-type="order">
<list-item>
<p>The concordance rate in evaluating invasive breast cancer profiles is 58.8%.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-83">83</xref>]</td>
<td>2023</td>
<td>Diagnosis</td>
<td>NA</td>
<td>NA</td>
<td>ChatGPT (Generative Pre-trained Transformer)-3.5 and GPT-4&#x2019;s (OpenAI, San Francisco, California)</td>
<td><list list-type="order">
<list-item>
<p>Both ChatGPT-3.5 and ChatGPT-4 attained an average OE score of 1.830 (out of 2) for breast cancer screening prompts. ChatGPT-3.5 demonstrated an average SATA accuracy of 88.9%, while ChatGPT-4 showed a higher average accuracy of 98.4% for these prompts.</p></list-item>
<list-item>
<p>For breast pain prompts, ChatGPT-3.5 scored an average OE of 1.125 (out of 2) and an average SATA accuracy of 58.3%, whereas ChatGPT-4 achieved an average OE score of 1.666 (out of 2) and a SATA accuracy of 77.7%.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-84">84</xref>]</td>
<td>2023</td>
<td>Diagnosis</td>
<td>Mammogram</td>
<td>Custom</td>
<td>Conditional GAN (CGAN)</td>
<td><list list-type="order">
<list-item>
<p>Four types of artifacts were identified, including checkerboard, breast boundary, nipple-areola complex, and black spots around calcification artifacts, with an overall incidence rate exceeding 69%. The individual incident rates varied between 9% and 53% across both normal and mammographically-occult cancer samples.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-85">85</xref>]</td>
<td>2023</td>
<td>Diagnosis</td>
<td>CT, MRI, PET, and digital X-ray images</td>
<td>DICOM datasets</td>
<td>Multi-class 3D U-Net with a pre-trained ResNet(2&#x002B;1)D-18 encoder branch, cascaded with a 2D PatchGAN</td>
<td><list list-type="order">
<list-item>
<p>The proposed method achieved mean Dice similarity coefficient values between 0.89 and 0.98, Hausdorff distance values ranging from 2.25 to 8.68 mm, and mean surface distance values varying from 0.62 to 2.79 mm.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-78">78</xref>]</td>
<td>2023</td>
<td>Diagnosis</td>
<td>Thermal imaging, mammography, MRI and ultrasonography</td>
<td>DMR dataset</td>
<td>Infrared-GAN</td>
<td><list list-type="order">
<list-item>
<p>The proposed model was assessed using three distinct datasets, resulting in a Dice score of 0.94 and a mean intersection over union of 0.932.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-86">86</xref>]</td>
<td>2023</td>
<td>Diagnosis</td>
<td>Digital X-ray images</td>
<td>Digital Database for Screening Mammography (DDSM) dataset</td>
<td>Multi-latent code inversion enhanced Generative Adversarial Network (dm-GAN)</td>
<td><list list-type="order">
<list-item>
<p>The proposed dm-GAN generates breast images with improved accuracy, achieving a 1.84 dB increase in Peak Signal-to-Noise Ratio (PSNR) and a 5.61% reduction in Fr&#x00E9;chet Inception Distance (FID).</p></list-item>
<list-item>
<p>It also produces images 1.38 times faster than the current state-of-the-art methods.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-24">24</xref>]</td>
<td>2023</td>
<td>Diagnosis</td>
<td>Ultrasonography</td>
<td>Custom</td>
<td>Large language model (LLM)</td>
<td><list list-type="order">
<list-item>
<p>Data were collected from 2931 patients.</p></list-item>
<list-item>
<p>The overall accuracy achieved was 87.7%.</p></list-item>
<list-item>
<p>The accuracy for lymphovascular invasion was 98.2%. Developing the prompts took 3.5 h, while processing them took 15 min.</p></list-item>
<list-item>
<p>Using the ChatGPT application programming interface incurred a cost of US $65.8, and when including the estimated wage, the total cost amounted to US $95.4. In a comparative estimation, both the &#x201C;LLM-assisted manual&#x201D; and &#x201C;LLM&#x201D; methods were found to be more time- and cost-efficient than the &#x201C;full manual&#x201D; approach.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-22">22</xref>]</td>
<td>2023</td>
<td>Diagnosis</td>
<td>Histopathology</td>
<td>BreakHis dataset</td>
<td>Gaussian-Laplacian pyramid and pyramid blending with similarity measures with GAN</td>
<td><list list-type="order">
<list-item>
<p>The impact of augmentation on the F1 score for 40x, 100x, 200x, and 400x histopathology images is 84.77%, 83.35%, 86.36%, and 83.73%, respectively.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-23">23</xref>]</td>
<td>2023</td>
<td>Diagnosis</td>
<td>Cytology images</td>
<td>Wisconsin Breast Cancer Diagnostic dataset &#x0026; Wisconsin Breast Cancer Prognostic Dataset</td>
<td>Tabular variational autoencoder (TVAE) and the conditional generative adversarial network (CTGAN)</td>
<td><list list-type="order">
<list-item>
<p>The proposed TVAE model outperformed in generating synthetic breast tumor data, achieving Chi-Squared test (CS test) scores of 0.916 (prognosis) and 0.964 (diagnosis), as well as Kolmogorov-Smirnov test (KS test) scores of 0.887 (prognosis) and 0.928 (diagnosis).</p></list-item>
<list-item>
<p>The proposed architecture outperformed all other machine learning and deep learning classifiers, achieving an accuracy of 96.66% in diagnosis and 82.83% in prognosis.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-27">27</xref>]</td>
<td>2022</td>
<td>Diagnosis</td>
<td>PET images</td>
<td>DICOM datasets</td>
<td>pix2pix GAN</td>
<td><list list-type="order">
<list-item>
<p>The quantitative evaluation of the proposed method showed significantly higher SSIM (<italic>p</italic> &#x003C; 0.01) and PSNR (<italic>p</italic> &#x003C; 0.01) for 26-second synthetic images, and higher PSNR for 52-second images (<italic>p</italic> &#x003C; 0.01) compared to the original images.</p></list-item>
<list-item>
<p>The proposed model enhanced the quality of low-count time dbPET synthetic images, with a more pronounced effect on images with lower counts.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-87">87</xref>]</td>
<td>2021</td>
<td>Diagnosis</td>
<td>Mammogram</td>
<td>Custom</td>
<td>AI-GAN</td>
<td><list list-type="order">
<list-item>
<p>The experiments showed that adversarial samples caused the AI-CAD model to produce incorrect diagnoses in 69.1% of cases that were initially classified correctly by the model.</p></list-item>
<list-item>
<p>The study highlights the critical need for ongoing research into the safety concerns of medical AI models and the development of potential defensive strategies against adversarial attacks.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-88">88</xref>]</td>
<td>2021</td>
<td>Diagnosis</td>
<td>Mammogram</td>
<td>CBIS-DDSM; Inbreast; Custom</td>
<td>Connected-Unets</td>
<td><list list-type="simple">
<list-item><label>1.</label><p>CBIS-DDSM Dice score: 89.52%</p></list-item>
<list-item>
<label>&#x2002;</label><p>IoU: 80.02%</p></list-item>
<list-item>
<label>&#x2002;</label><p>INbreast Dice score: 95.28%</p></list-item>
<list-item>
<label>&#x2002;</label><p>IoU: 91.03%</p></list-item>
<list-item>
<label>&#x2002;</label><p>Custom Dice score: 95.88%</p></list-item>
<list-item>
<label>&#x2002;</label><p>IoU: 92.27%</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-89">89</xref>]</td>
<td>2021</td>
<td>Diagnosis</td>
<td>Histopathology</td>
<td>Custom</td>
<td>Generative Adversarial Network for Distribution Analysis (GANDA)</td>
<td><list list-type="order">
<list-item>
<p>The GANDA model can conditionally generate images depicting intratumoral quantum dot (QD) distribution, constrained by the tumor vessels and cell nuclei channels, while preserving the same spatial resolution (pixel-to-pixel).</p></list-item>
<list-item>
<p>It demonstrates minimal loss (mean squared error, MSE &#x003D; 1.871) and high reliability (intraclass correlation, ICC &#x003D; 0.94).</p></list-item>
<list-item>
<p>This capability enables quantitative analysis of QD extravasation distance (ICC &#x003D; 0.95) and subarea distribution (ICC &#x003D; 0.99) on the generated images, without needing the actual QD distribution data.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-90">90</xref>]</td>
<td>2020</td>
<td>Diagnosis</td>
<td>Fluorescence images</td>
<td>Custom</td>
<td>Virtual-fluorescence-staining method based on deep neural networks (VirFluoNet)</td>
<td><list list-type="order">
<list-item>
<p>Utilizing deep learning to virtually generate fluorescence images can significantly lower the cost, time, and effort involved in sample preparation, including processes like chemical fixation and staining.</p></list-item>
<list-item>
<p>The mean absolute error (MAE) is &#x003C;0.005, 0.017, and 0.012 for 4<sup>&#x2032;</sup>,6-diamidino-2-phenylindole/hoechst, endoplasmic reticulum, and mitochondria prediction, respectively.</p></list-item>
<list-item>
<p>The peak signal-to-noise ratio (PSNR) exceeds 40/34/33 dB, and the structural similarity index (SSIM) is greater than 0.925/0.926/0.925 for the same predictions.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-65">65</xref>]</td>
<td>2020</td>
<td>Diagnosis</td>
<td>Cone-beam computed tomography</td>
<td>Custom</td>
<td>Three cycle-consistent generative adversarial networks (cycle- GANs)</td>
<td><list list-type="order">
<list-item>
<p>A synthetic computed tomography image was generated in 10 s.</p></list-item>
<list-item>
<p>Image similarity was similar between models trained on various anatomical sites and a single model for all sites.</p></list-item>
<list-item>
<p>Mean dose differences of less than 0.5% were observed in high-dose regions.</p></list-item>
<list-item>
<p>Mean gamma (3%, 3 mm) pass rates were obtained across all sites.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-91">91</xref>]</td>
<td>2019</td>
<td>Diagnosis</td>
<td>Ultrasonography</td>
<td>Custom</td>
<td>Deep convolutional generative adversarial networks (DCGANs)</td>
<td><list list-type="order">
<list-item>
<p>The proposed DCGAN is capable of generating high-quality, realistic synthetic breast ultrasound images that are indistinguishable from the original ones.</p></list-item>
<list-item>
<p>Interobserver agreement was excellent, with correlation values (|r|) ranging from 0.708 to 0.825 (<italic>p</italic> &#x003C; 0.001).</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-92">92</xref>]</td>
<td>2019</td>
<td>Diagnosis</td>
<td>Mammogram</td>
<td>BCDR; INbreast</td>
<td>Cycle-consistent GANs model (CycleGAN)</td>
<td><list list-type="order">
<list-item>
<p>At the lower resolution, the overall performance remained unaffected by the CycleGAN modifications (AUC 0.70 vs. 0.76, <italic>p</italic> &#x003D; 0.67).</p></list-item>
<list-item>
<p>One radiologist demonstrated a decrease in cancer detection (0.85 vs. 0.63, <italic>p</italic> &#x003D; 0.06).</p></list-item>
<list-item>
<p>At the higher resolution, all radiologists showed a significantly reduced cancer detection rate in the modified images (0.80 vs. 0.37, <italic>p</italic> &#x003C; 0.001).</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-93">93</xref>]</td>
<td>2018</td>
<td>Diagnosis</td>
<td>Peptides data</td>
<td>Custom</td>
<td>Recurrent neural network with long short-term memory cells</td>
<td><list list-type="order">
<list-item>
<p>Six of the active peptides selectively targeted and killed MCF7 cancer cells with at least three times the specificity, without affecting human erythrocytes.</p></list-item>
<list-item>
<p>These results validate the application of constructive machine learning in the automated design of peptides with specific biological activities.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-94">94</xref>]</td>
<td>2016</td>
<td>Diagnosis</td>
<td>Molecules data</td>
<td>Molecules data (Human intestinal transporter database: QSAR modeling and virtual profiling of drug uptake, efflux and interactions)</td>
<td>Generative topographic mapping (GTM)</td>
<td><list list-type="order">
<list-item>
<p>The proposed GTM is employed to create 21 classification models that correlate the structure of organic molecules with their inhibition and transport activities for 11 transporters.</p></list-item>
<list-item>
<p>These models deliver predictive performance on par with well-known machine learning techniques like kNN, Random Forest, and Support Vector Machine.</p></list-item>
<list-item>
<p>A distinctive GTM-based applicability domain definition helps remove uncertainty regions, thereby improving the models&#x2019; performance.</p></list-item>
</list></td>
</tr>
<tr align="center">
<td>[<xref ref-type="bibr" rid="ref-95">95</xref>]</td>
<td>2007</td>
<td>Diagnosis</td>
<td>Gene expression data</td>
<td>Breast cancer data (Gene expression profiles in hereditary breast cancer)</td>
<td>Hierarchical statistical model: kernel-imbedded Gaussian process (KIGP)</td>
<td><list list-type="order">
<list-item>
<p>Simulation studies demonstrated that the KIGP performed nearly as well as the theoretical Bayesian bound, with no prior knowledge of the underlying generative model.</p></list-item>
<list-item>
<p>This high performance was observed not only with a linear Bayesian classifier but also with a highly non-linear Bayesian classifier.</p></list-item>
</list></td></tr>
</tbody>
</table>
</table-wrap>
</app>
<app id="app-3"><title>Appendix C</title>
<table-wrap id="table-7">
<label>Table A2</label>
<caption>
<title>The PRISMA checklist</title>
</caption>
<table>
<colgroup>
<col align="center"/>
<col/>
<col align="center"/>
<col align="center"/>
</colgroup>
<thead>
<tr align="center">
<th align="center">Section and topic</th>
<th>Item #</th>
<th align="center">Checklist item</th>
<th align="center">Location where item is reported</th>
</tr>
</thead>
<tbody>
<tr align="center">
<td><bold>TITLE</bold></td>
<td/>
<td/>
<td/>
</tr>
<tr align="center">
<td>Title</td>
<td>1</td>
<td>Identify the report as a systematic review.</td>
<td>Title</td>
</tr>
<tr align="center">
<td><bold>ABSTRACT</bold></td>
<td/>
<td/>
<td/>
</tr>
<tr align="center">
<td>Abstract</td>
<td>2</td>
<td>See the PRISMA 2020 for Abstracts checklist.</td>
<td>Abstract</td>
</tr>
<tr align="center">
<td><bold>INTRODUCTION</bold></td>
<td/>
<td/>
<td/>
</tr>
<tr align="center">
<td>Rationale</td>
<td>3</td>
<td>Describe the rationale for the review in the context of existing knowledge.</td>
<td><xref ref-type="sec" rid="s1_3">Section 1.3</xref></td>
</tr>
<tr align="center">
<td>Objectives</td>
<td>4</td>
<td>Provide an explicit statement of the objective(s) or question(s) the review addresses.</td>
<td><xref ref-type="sec" rid="s1_3">Section 1.3</xref></td>
</tr>
<tr align="center">
<td><bold>METHODS</bold></td>
<td/>
<td/>
<td/>
</tr>
<tr align="center">
<td>Eligibility criteria</td>
<td>5</td>
<td>Specify the inclusion and exclusion criteria for the review and how studies were grouped for the syntheses.</td>
<td><xref ref-type="sec" rid="s3_2">Section 3.2</xref></td>
</tr>
<tr align="center">
<td>Information sources</td>
<td>6</td>
<td>Specify all databases, registers, websites, organisations, reference lists and other sources searched or consulted to identify studies. Specify the date when each source was last searched or consulted.</td>
<td><xref ref-type="sec" rid="s3_1">Section 3.1</xref></td>
</tr>
<tr align="center">
<td>Search strategy</td>
<td>7</td>
<td>Present the full search strategies for all databases, registers and websites, including any filters and limits used.</td>
<td><xref ref-type="sec" rid="s3_1">Section 3.1</xref></td>
</tr>
<tr align="center">
<td>Selection process</td>
<td>8</td>
<td>Specify the methods used to decide whether a study met the inclusion criteria of the review, including how many reviewers screened each record and each report retrieved, whether they worked independently, and if applicable, details of automation tools used in the process.</td>
<td><xref ref-type="sec" rid="s3_3">Section 3.3</xref></td>
</tr>
<tr align="center">
<td>Data collection process</td>
<td>9</td>
<td>Specify the methods used to collect data from reports, including how many reviewers collected data from each report, whether they worked independently, any processes for obtaining or confirming data from study investigators, and if applicable, details of automation tools used in the process.</td>
<td><xref ref-type="sec" rid="s3_1">Sections 3.1</xref> &#x0026; <xref ref-type="sec" rid="s3_2_1">3.2.1</xref></td>
</tr>
<tr align="center">
<td>Data items</td>
<td>10a</td>
<td>List and define all outcomes for which data were sought. Specify whether all results that were compatible with each outcome domain in each study were sought (e.g., for all measures, time points, analyses), and if not, the methods used to decide which results to collect.</td>
<td><xref ref-type="table" rid="table-6">Table A1</xref></td>
</tr>
<tr align="center">
<td></td>
<td>10b</td>
<td>List and define all other variables for which data were sought (e.g., participant and intervention characteristics, funding sources). Describe any assumptions made about any missing or unclear information.</td>
<td><xref ref-type="table" rid="table-6">Table A1</xref></td>
</tr>
<tr align="center">
<td>Study risk of bias assessment</td>
<td>11</td>
<td>Specify the methods used to assess risk of bias in the included studies, including details of the tool(s) used, how many reviewers assessed each study and whether they worked independently, and if applicable, details of automation tools used in the process.</td>
<td><xref ref-type="sec" rid="s5_2">Section 5.2</xref></td>
</tr>
<tr align="center">
<td>Effect measures</td>
<td>12</td>
<td>Specify for each outcome the effect measure(s) (e.g., risk ratio, mean difference) used in the synthesis or presentation of results.</td>
<td>NA (Meta-analysis not performed)</td>
</tr>
<tr align="center">
<td>Synthesis methods</td>
<td>13a</td>
<td>Describe the processes used to decide which studies were eligible for each synthesis (e.g., tabulating the study intervention characteristics and comparing against the planned groups for each synthesis (item #5)).</td>
<td><xref ref-type="sec" rid="s3_2_1">Section 3.2.1</xref></td>
</tr>
<tr align="center">
<td></td>
<td>13b</td>
<td>Describe any methods required to prepare the data for presentation or synthesis, such as handling of missing summary statistics, or data conversions.</td>
<td><xref ref-type="sec" rid="s3_3">Section 3.3</xref></td>
</tr>
<tr align="center">
<td></td>
<td>13c</td>
<td>Describe any methods used to tabulate or visually display results of individual studies and syntheses.</td>
<td><xref ref-type="sec" rid="s3_3">Section 3.3</xref></td>
</tr>
<tr align="center">
<td></td>
<td>13d</td>
<td>Describe any methods used to synthesize results and provide a rationale for the choice(s). If meta-analysis was performed, describe the model(s), method(s) to identify the presence and extent of statistical heterogeneity, and software package(s) used.</td>
<td><xref ref-type="sec" rid="s3_3">Section 3.3</xref> (Meta-analysis not performed)</td>
</tr>
<tr align="center">
<td></td>
<td>13e</td>
<td>Describe any methods used to explore possible causes of heterogeneity among study results (e.g., subgroup analysis, meta-regression).</td>
<td>NA (Meta-analysis not performed)</td>
</tr>
<tr align="center">
<td></td>
<td>13f</td>
<td>Describe any sensitivity analyses conducted to assess robustness of the synthesized results.</td>
<td>NA (Meta-analysis not performed)</td>
</tr>
<tr align="center">
<td>Reporting bias assessment</td>
<td>14</td>
<td>Describe any methods used to assess risk of bias due to missing results in a synthesis (arising from reporting biases).</td>
<td><xref ref-type="sec" rid="s5_2">Section 5.2</xref></td>
</tr>
<tr align="center">
<td>Certainty assessment</td>
<td>15</td>
<td>Describe any methods used to assess certainty (or confidence) in the body of evidence for an outcome.</td>
<td>NA (Meta-analysis not performed)</td>
</tr>
<tr align="center">
<td><bold>RESULTS</bold></td>
<td/>
<td/>
<td/>
</tr>
<tr align="center">
<td>Study selection</td>
<td>16a</td>
<td>Describe the results of the search and selection process, from the number of records identified in the search to the number of studies included in the review, ideally using a flow diagram.</td>
<td><xref ref-type="fig" rid="fig-4">Fig. 4</xref></td>
</tr>
<tr align="center">
<td></td>
<td>16b</td>
<td>Cite studies that might appear to meet the inclusion criteria, but which were excluded, and explain why they were excluded.</td>
<td><xref ref-type="sec" rid="s3_2_1">Section 3.2.1</xref></td>
</tr>
<tr align="center">
<td>Study characteristics</td>
<td>17</td>
<td>Cite each included study and present its characteristics.</td>
<td><xref ref-type="table" rid="table-6">Table A1</xref></td>
</tr>
<tr align="center">
<td>Risk of bias in studies</td>
<td>18</td>
<td>Present assessments of risk of bias for each included study.</td>
<td>NA (Meta-analysis not performed)</td>
</tr>
<tr align="center">
<td>Results of individual studies</td>
<td>19</td>
<td>For all outcomes, present, for each study: (a) summary statistics for each group (where appropriate) and (b) an effect estimate and its precision (e.g., confidence/credible interval), ideally using structured tables or plots.</td>
<td><xref ref-type="table" rid="table-6">Table A1</xref></td>
</tr>
<tr align="center">
<td>Results of syntheses</td>
<td>20a</td>
<td>For each synthesis, briefly summarise the characteristics and risk of bias among contributing studies.</td>
<td>NA (Meta-analysis not performed)</td>
</tr>
<tr align="center">
<td></td>
<td>20b</td>
<td>Present results of all statistical syntheses conducted. If meta-analysis was done, present for each the summary estimate and its precision (e.g., confidence/credible interval) and measures of statistical heterogeneity. If comparing groups, describe the direction of the effect.</td>
<td>NA (Meta-analysis not performed)</td>
</tr>
<tr align="center">
<td></td>
<td>20c</td>
<td>Present results of all investigations of possible causes of heterogeneity among study results.</td>
<td>NA (Meta-analysis not performed)</td>
</tr>
<tr align="center">
<td></td>
<td>20d</td>
<td>Present results of all sensitivity analyses conducted to assess the robustness of the synthesized results.</td>
<td>NA (Meta-analysis not performed)</td>
</tr>
<tr align="center">
<td>Reporting biases</td>
<td>21</td>
<td>Present assessments of risk of bias due to missing results (arising from reporting biases) for each synthesis assessed.</td>
<td><xref ref-type="sec" rid="s5_2">Section 5.2</xref></td>
</tr>
<tr align="center">
<td>Certainty of evidence</td>
<td>22</td>
<td>Present assessments of certainty (or confidence) in the body of evidence for each outcome assessed.</td>
<td><xref ref-type="sec" rid="s5_2">Section 5.2</xref></td>
</tr>
<tr align="center">
<td><bold>DISCUSSION</bold></td>
<td/>
<td/>
<td/>
</tr>
<tr align="center">
<td>Discussion</td>
<td>23a</td>
<td>Provide a general interpretation of the results in the context of other evidence.</td>
<td><xref ref-type="table" rid="table-6">Table A1</xref> &#x0026; <xref ref-type="sec" rid="s5_3">Section 5.3</xref></td>
</tr>
<tr align="center">
<td></td>
<td>23b</td>
<td>Discuss any limitations of the evidence included in the review.</td>
<td><xref ref-type="sec" rid="s5_2">Section 5.2</xref></td>
</tr>
<tr align="center">
<td></td>
<td>23c</td>
<td>Discuss any limitations of the review processes used.</td>
<td><xref ref-type="sec" rid="s5_2">Section 5.2</xref></td>
</tr>
<tr align="center">
<td></td>
<td>23d</td>
<td>Discuss implications of the results for practice, policy, and future research.</td>
<td><xref ref-type="sec" rid="s5_3">Sections 5.3</xref> &#x0026; <xref ref-type="sec" rid="s6">6</xref></td>
</tr>
<tr align="center">
<td><bold>OTHER INFORMATION</bold></td>
<td/>
<td/>
<td/>
</tr>
<tr align="center">
<td>Registration and protocol</td>
<td>24a</td>
<td>Provide registration information for the review, including register name and registration number, or state that the review was not registered.</td>
<td>Ethics Approval statement</td>
</tr>
<tr align="center">
<td></td>
<td>24b</td>
<td>Indicate where the review protocol can be accessed, or state that a protocol was not prepared.</td>
<td>Ethics Approval statement</td>
</tr>
<tr align="center">
<td></td>
<td>24c</td>
<td>Describe and explain any amendments to information provided at registration or in the protocol.</td>
<td>Ethics Approval statement</td>
</tr>
<tr align="center">
<td>Support</td>
<td>25</td>
<td>Describe sources of financial or non-financial support for the review, and the role of the funders or sponsors in the review.</td>
<td>Funding statement</td>
</tr>
<tr align="center">
<td>Competing interests</td>
<td>26</td>
<td>Declare any competing interests of review authors.</td>
<td>Conflicts of Interest statement</td>
</tr>
<tr align="center">
<td>Availability of data, code and other materials</td>
<td>27</td>
<td>Report which of the following are publicly available and where they can be found: template data collection forms; data extracted from included studies; data used for all analyses; analyticx` code; any other materials used in the review.</td>
<td>Availability of Data and Materials statement</td>
</tr>
</tbody>
</table>
</table-wrap><table-wrap id="table-8">
<label>Table A3</label>
<caption>
<title>PRISMA 2020 for Abstracts Checklist</title>
</caption>
<table>
<colgroup>
<col align="left"/>
<col align="center"/>
<col align="center"/>
<col align="center"/>
</colgroup>
<thead>
<tr align="center">
<th align="left">Section and Topic</th>
<th align="center">Item #</th>
<th align="center">Checklist item</th>
<th align="center">Reported (Yes/No)</th>
</tr>
</thead>
<tbody>
<tr align="center">
<td align="left"><bold>TITLE</bold></td>
<td></td>
<td></td>
<td></td>
</tr>
<tr align="center">
<td>Title</td>
<td>1</td>
<td>Identify the report as a systematic review.</td>
<td>Yes</td>
</tr>
<tr align="center">
<td align="left"><bold>BACKGROUND</bold></td>
<td></td>
<td></td>
<td></td>
</tr>
<tr align="center">
<td>Objectives</td>
<td>2</td>
<td>Provide an explicit statement of the main objective(s) or question(s) the review addresses.</td>
<td>Yes</td>
</tr>
<tr align="center">
<td align="left"><bold>METHODS</bold></td>
<td></td>
<td></td>
<td></td>
</tr>
<tr align="center">
<td>Eligibility criteria</td>
<td>3</td>
<td>Specify the inclusion and exclusion criteria for the review.</td>
<td>Yes</td>
</tr>
<tr align="center">
<td>Information sources</td>
<td>4</td>
<td>Specify the information sources (e.g. databases, registers) used to identify studies and the date when each was last searched.</td>
<td>Yes</td>
</tr>
<tr align="center">
<td>Risk of bias</td>
<td>5</td>
<td>Specify the methods used to assess risk of bias in the included studies.</td>
<td>Yes</td>
</tr>
<tr align="center">
<td>Synthesis of results</td>
<td>6</td>
<td>Specify the methods used to present and synthesise results.</td>
<td>Yes</td>
</tr>
<tr align="center">
<td align="left"><bold>RESULTS</bold></td>
<td></td>
<td></td>
<td></td>
</tr>
<tr align="center">
<td>Included studies</td>
<td>7</td>
<td>Give the total number of included studies and participants and summarise relevant characteristics of studies.</td>
<td>Yes</td>
</tr>
<tr align="center">
<td>Synthesis of results</td>
<td>8</td>
<td>Present results for main outcomes, preferably indicating the number of included studies and participants for each. If meta-analysis was done, report the summary estimate and confidence/credible interval. If comparing groups, indicate the direction of the effect (i.e. which group is favoured).</td>
<td>Yes, the number of included studies is provided, a meta-analysis was not performed in this study</td>
</tr>
<tr align="center">
<td align="left"><bold>DISCUSSION</bold></td>
<td></td>
<td></td>
<td></td>
</tr>
<tr align="center">
<td>Limitations of evidence</td>
<td>9</td>
<td>Provide a brief summary of the limitations of the evidence included in the review (e.g. study risk of bias, inconsistency and imprecision).</td>
<td>Yes</td>
</tr>
<tr align="center">
<td>Interpretation</td>
<td>10</td>
<td>Provide a general interpretation of the results and important implications.</td>
<td>Yes</td>
</tr>
<tr align="center">
<td align="left"><bold>OTHER</bold></td>
<td></td>
<td></td>
<td></td>
</tr>
<tr align="center">
<td>Funding</td>
<td>11</td>
<td>Specify the primary source of funding for the review.</td>
<td>Yes</td>
</tr>
<tr align="center">
<td>Registration</td>
<td>12</td>
<td>Provide the register name and registration number.</td>
<td>Yes</td>
</tr>
</tbody>
</table>
<table-wrap-foot><fn id="table-8fn1" fn-type="other"><p><italic>From:</italic> Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ 2021;372:n71. doi: 10.1136/bmj.n71. For more information, visit: http://www.prisma-statement.org/</p></fn></table-wrap-foot>
</table-wrap>
</app>
</app-group>
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