Bikash Santra, Abhishek Jha, Pritam Mukherjee, Mayank Patel, Karel Pacak, Ronald M Summers
{"title":"Anatomical Location-Guided Deep Learning-Based Genetic Cluster Identification of Pheochromocytomas and Paragangliomas From CT Images.","authors":"Bikash Santra, Abhishek Jha, Pritam Mukherjee, Mayank Patel, Karel Pacak, Ronald M Summers","doi":"10.1007/978-3-031-47076-9_7","DOIUrl":null,"url":null,"abstract":"<p><p>Pheochromocytomas and paragangliomas (PPGLs) are respectively intra-adrenal and extra-adrenal neuroendocrine tumors whose pathogenesis and progression are greatly regulated by genetics. Identifying PPGL's genetic clusters (<i>SDHx</i>, <i>VHL/EPAS1</i>, <i>kinase signaling</i>, and sporadic) is essential as PPGL's management varies critically on its genotype. But, genetic testing for PPGLs is expensive and time-consuming. Contrast-enhanced CT (CE-CT) scans of PPGL patients are usually acquired at the beginning of patient management for PPGL staging and determining the next therapeutic steps. Given a CE-CT sub-image of the PPGL, this work demonstrates a two-branch vision transformer (<i>PPGL-Transformer</i>) to identify each tumor's genetic cluster. The standard of reference for each tumor included two items: its genetic cluster from clinical testing, and its anatomical location. One branch of our <i>PPGL-Transformer</i> identifies PPGL's anatomic location while the other one characterizes PPGL's genetic type. A supervised contrastive learning strategy was used to train the <i>PPGL-Transformer</i> by optimizing contrastive and classification losses for PPGLs' genetic group and anatomic location. Our method was evaluated on a dataset comprised of 1010 PPGLs extracted from the CE-CT images of 289 patients. <i>PPGL-Transformer</i> achieved an accuracy of 0.63±0.08, balanced accuracy (BA) of 0.63±0.06 and F1-score of 0.46±0.08 on five-fold cross-validation and outperformed competing methods by 2-29% on accuracy, 3-18% on BA and 3-14% on F1-score. The performance for the sporadic cluster was higher on BA (0.68 ± 0.13) while the performance for the <i>SDHx</i> cluster was higher on recall (0.83 ± 0.06) and F1-score (0.74 ± 0.07).</p>","PeriodicalId":520534,"journal":{"name":"Applications of Medical Artificial Intelligence : Second International Workshop, AMAI 2023, Held in Conjunction with MICCAI 2023, Vancouver, BC, Canada, October 8, 2023, Proceedings","volume":"14313 ","pages":"62-71"},"PeriodicalIF":0.0000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12060173/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applications of Medical Artificial Intelligence : Second International Workshop, AMAI 2023, Held in Conjunction with MICCAI 2023, Vancouver, BC, Canada, October 8, 2023, Proceedings","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/978-3-031-47076-9_7","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/10/26 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Pheochromocytomas and paragangliomas (PPGLs) are respectively intra-adrenal and extra-adrenal neuroendocrine tumors whose pathogenesis and progression are greatly regulated by genetics. Identifying PPGL's genetic clusters (SDHx, VHL/EPAS1, kinase signaling, and sporadic) is essential as PPGL's management varies critically on its genotype. But, genetic testing for PPGLs is expensive and time-consuming. Contrast-enhanced CT (CE-CT) scans of PPGL patients are usually acquired at the beginning of patient management for PPGL staging and determining the next therapeutic steps. Given a CE-CT sub-image of the PPGL, this work demonstrates a two-branch vision transformer (PPGL-Transformer) to identify each tumor's genetic cluster. The standard of reference for each tumor included two items: its genetic cluster from clinical testing, and its anatomical location. One branch of our PPGL-Transformer identifies PPGL's anatomic location while the other one characterizes PPGL's genetic type. A supervised contrastive learning strategy was used to train the PPGL-Transformer by optimizing contrastive and classification losses for PPGLs' genetic group and anatomic location. Our method was evaluated on a dataset comprised of 1010 PPGLs extracted from the CE-CT images of 289 patients. PPGL-Transformer achieved an accuracy of 0.63±0.08, balanced accuracy (BA) of 0.63±0.06 and F1-score of 0.46±0.08 on five-fold cross-validation and outperformed competing methods by 2-29% on accuracy, 3-18% on BA and 3-14% on F1-score. The performance for the sporadic cluster was higher on BA (0.68 ± 0.13) while the performance for the SDHx cluster was higher on recall (0.83 ± 0.06) and F1-score (0.74 ± 0.07).