Abstract

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.

Endometrial cancer (EC) has four molecular subtypes; of these, the No Specific Molecular Profile (NSMP) subtype encompasses patients with heterogeneous outcomes. Here, the authors use artificial intelligence and histopathology images to differentiate p53abn and NSMP subtypes in EC, and identify one distinct subgroup within NSMP with unfavourable outcome.

Details

Title
AI-based histopathology image analysis reveals a distinct subset of endometrial cancers
Author
Darbandsari, Amirali 1 ; Farahani, Hossein 2   VIAFID ORCID Logo  ; Asadi, Maryam 3 ; Wiens, Matthew 3 ; Cochrane, Dawn 4 ; Khajegili Mirabadi, Ali 3   VIAFID ORCID Logo  ; Jamieson, Amy 5 ; Farnell, David 6 ; Ahmadvand, Pouya 3 ; Douglas, Maxwell 4 ; Leung, Samuel 4 ; Abolmaesumi, Purang 1 ; Jones, Steven J. M. 7   VIAFID ORCID Logo  ; Talhouk, Aline 5 ; Kommoss, Stefan 8 ; Gilks, C. Blake 6 ; Huntsman, David G. 9 ; Singh, Naveena 6 ; McAlpine, Jessica N. 5   VIAFID ORCID Logo  ; Bashashati, Ali 2   VIAFID ORCID Logo 

 University of British Columbia, Department of Electrical and Computer Engineering, Vancouver, Canada (GRID:grid.17091.3e) (ISNI:0000 0001 2288 9830) 
 University of British Columbia, School of Biomedical Engineering, Vancouver, Canada (GRID:grid.17091.3e) (ISNI:0000 0001 2288 9830); University of British Columbia, Department of Pathology and Laboratory Medicine, Vancouver, Canada (GRID:grid.17091.3e) (ISNI:0000 0001 2288 9830) 
 University of British Columbia, School of Biomedical Engineering, Vancouver, Canada (GRID:grid.17091.3e) (ISNI:0000 0001 2288 9830) 
 British Columbia Cancer Research Institute, Department of Molecular Oncology, Vancouver, Canada (GRID:grid.17091.3e) 
 University of British Columbia, Department of Obstetrics and Gynaecology, Vancouver, Canada (GRID:grid.17091.3e) (ISNI:0000 0001 2288 9830) 
 University of British Columbia, Department of Pathology and Laboratory Medicine, Vancouver, Canada (GRID:grid.17091.3e) (ISNI:0000 0001 2288 9830); Vancouver General Hospital, Vancouver, Canada (GRID:grid.412541.7) (ISNI:0000 0001 0684 7796) 
 British Columbia Cancer Research Center, Michael Smith Genome Sciences Center, Vancouver, Canada (GRID:grid.248762.d) (ISNI:0000 0001 0702 3000) 
 Tübingen University Hospital, Department of Women’s Health, Tübingen, Germany (GRID:grid.10392.39) (ISNI:0000 0001 2190 1447) 
 University of British Columbia, Department of Pathology and Laboratory Medicine, Vancouver, Canada (GRID:grid.17091.3e) (ISNI:0000 0001 2288 9830); British Columbia Cancer Research Institute, Department of Molecular Oncology, Vancouver, Canada (GRID:grid.17091.3e) 
Pages
4973
Publication year
2024
Publication date
2024
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
3072375728
Copyright
© The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.