A Pan-Cancer Patient-Derived Xenograft Histology Image Repository with Genomic and Pathologic Annotations Enables Deep Learning Analysis.
СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАResearch Support, N.I.H., IntramuralНазвание и аннотация: Перевод пока не подготовлен
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White Brian S, Woo Xing Yi, Koc Soner, Sheridan Todd, Neuhauser Steven B, Wang Shidan, Evrard Yvonne A, Chen Li, Foroughi Pour Ali, Landua John D, Mashl R Jay, Davies Sherri R, Fang Bingliang, Raso Maria Gabriela, Evans Kurt W, Bailey Matthew H, Chen Yeqing, Xiao Min, Rubinstein Jill C, Sanderson Brian J, Lloyd Michael W, Domanskyi Sergii, Dobrolecki Lacey E, Fujita Maihi, Fujimoto Junya, Xiao Guanghua, Fields Ryan C, Mudd Jacqueline L, Xu Xiaowei, Hollingshead Melinda G, Jiwani Shahanawaz, Acevedo Saul, PDXNet Consortium, Davis-Dusenbery Brandi N, Robinson Peter N, Moscow Jeffrey A, Doroshow James H, Mitsiades Nicholas, Kaochar Salma, Pan Chong-Xian, Carvajal-Carmona Luis G, Welm Alana L, Welm Bryan E, Govindan Ramaswamy, Li Shunqiang, Davies Michael A, Roth Jack A, Meric-Bernstam Funda, Xie Yang, Herlyn Meenhard, Ding Li, Lewis Michael T, Bult Carol J, Dean Dennis A, Chuang Jeffrey H
Аннотация
Patient-derived xenografts (PDX) model human intra- and intertumoral heterogeneity in the context of the intact tissue of immunocompromised mice. Histologic imaging via hematoxylin and eosin (H&E) staining is routinely performed on PDX samples, which could be harnessed for computational analysis. Prior studies of large clinical H&E image repositories have shown that deep learning analysis can identify intercellular and morphologic signals correlated with disease phenotype and therapeutic response. In this study, we developed an extensive, pan-cancer repository of >1,000 PDX and paired parental tumor H&E images. These images, curated from the PDX Development and Trial Centers Research Network Consortium, had a range of associated genomic and transcriptomic data, clinical metadata, pathologic assessments of cell composition, and, in several cases, detailed pathologic annotations of neoplastic, stromal, and necrotic regions. The amenability of these images to deep learning was highlighted through three applications: (i) development of a classifier for neoplastic, stromal, and necrotic regions; (ii) development of a predictor of xenograft-transplant lymphoproliferative disorder; and (iii) application of a published predictor of microsatellite instability. Together, this PDX Development and Trial Centers Research Network image repository provides a valuable resource for controlled digital pathology analysis, both for the evaluation of technical issues and for the development of computational image-based methods that make clinical predictions based on PDX treatment studies. Significance: A pan-cancer repository of >1,000 patient-derived xenograft hematoxylin and eosin-stained images will facilitate cancer biology investigations through histopathologic analysis and contributes important model system data that expand existing human histology repositories.