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Prediction of recurrence risk in endometrial cancer with multimodal deep learning

  • Sarah Volinsky-Fremond
  • , Nanda Horeweg
  • , Sonali Andani
  • , Jurriaan Barkey Wolf
  • , Maxime W. Lafarge
  • , Cor D. de Kroon
  • , Gitte Ørtoft
  • , Estrid Høgdall
  • , Jouke Dijkstra
  • , Jan J. Jobsen
  • , Ludy C.H.W. Lutgens
  • , Melanie E. Powell
  • , Linda R. Mileshkin
  • , Helen Mackay
  • , Alexandra Leary
  • , Dionyssios Katsaros
  • , Hans W. Nijman
  • , Stephanie M. de Boer
  • , Remi A. Nout
  • , Marco de Bruyn
  • David Church, Vincent T.H.B.M. Smit, Carien L. Creutzberg, Viktor H. Koelzer, Tjalling Bosse*
*Corresponding author for this work
  • Leiden University
  • Leiden University Medical Centre
  • Swiss Federal Institute of Technology Zurich
  • University Hospital Zürich
  • Swiss Institute of Bioinformatics
  • Rigshospitalet
  • Copenhagen University Hospital (Nordvest)
  • Medisch Spectrum Twente
  • Maastricht University Medical Centre
  • Barts Health NHS Trust
  • Peter Maccallum Cancer Centre
  • Sunnybrook Research Institute
  • Institut Gustave Roussy
  • University of Turin
  • University Medical Centre Groningen
  • University of Oxford
  • NIHR Biomedical Research Centres
  • Universitätsspital Basel

Research output: Contribution to journalArticleAcademicpeer-review

71 Citations (Scopus)
137 Downloads (Pure)

Abstract

Predicting distant recurrence of endometrial cancer (EC) is crucial for personalized adjuvant treatment. The current gold standard of combined pathological and molecular profiling is costly, hampering implementation. Here we developed HECTOR (histopathology-based endometrial cancer tailored outcome risk), a multimodal deep learning prognostic model using hematoxylin and eosin-stained, whole-slide images and tumor stage as input, on 2,072 patients from eight EC cohorts including the PORTEC-1/-2/-3 randomized trials. HECTOR demonstrated C-indices in internal (n = 353) and two external (n = 160 and n = 151) test sets of 0.789, 0.828 and 0.815, respectively, outperforming the current gold standard, and identified patients with markedly different outcomes (10-year distant recurrence-free probabilities of 97.0%, 77.7% and 58.1% for HECTOR low-, intermediate- and high-risk groups, respectively, by Kaplan–Meier analysis). HECTOR also predicted adjuvant chemotherapy benefit better than current methods. Morphological and genomic feature extraction identified correlates of HECTOR risk groups, some with therapeutic potential. HECTOR improves on the current gold standard and may help delivery of personalized treatment in EC.

Original languageEnglish
Pages (from-to)1962-1973
Number of pages12
JournalNature Medicine
Volume30
Issue number7
DOIs
Publication statusPublished - Jul 2024

Bibliographical note

Publisher Copyright:
© The Author(s) 2024. corrected publication 2024.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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