组织病理学
子宫内膜癌
肿瘤科
生物
内科学
癌症
病理
计算生物学
医学
生物信息学
作者
Amirali Darbandsari,Hossein Farahani,Maryam Asadi,Matthew O. Wiens,Dawn R. Cochrane,Ali Khajegili Mirabadi,Amy Jamieson,David Farnell,Pouya Ahmadvand,Maxwell Douglas,Samuel Leung,Purang Abolmaesumi,Steven J.M. Jones,Aline Talhouk,Stefan Kommoss,C. Blake Gilks,David G. Huntsman,Naveena Singh,Jessica N. McAlpine,Ali Bashashati
标识
DOI:10.1038/s41467-024-49017-2
摘要
Endometrial cancer (EC) has four molecular subtypes with strong prognostic value and therapeutic implications. The most common subtype (NSMP; No Specific Molecular Profile) is assigned after exclusion of the defining features of the other three molecular subtypes and includes patients with heterogeneous clinical outcomes. In this study, we employ artificial intelligence (AI)-powered histopathology image analysis to differentiate between p53abn and NSMP EC subtypes and consequently identify a sub-group of NSMP EC patients that has markedly inferior progression-free and disease-specific survival (termed 'p53abn-like NSMP'), in a discovery cohort of 368 patients and two independent validation cohorts of 290 and 614 from other centers. Shallow whole genome sequencing reveals a higher burden of copy number abnormalities in the 'p53abn-like NSMP' group compared to NSMP, suggesting that this group is biologically distinct compared to other NSMP ECs. Our work demonstrates the power of AI to detect prognostically different and otherwise unrecognizable subsets of EC where conventional and standard molecular or pathologic criteria fall short, refining image-based tumor classification. This study's findings are applicable exclusively to females.
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