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The impact of site-specific digital histology signatures on deep learning model accuracy and bias

Author

Listed:
  • Frederick M. Howard

    (University of Chicago)

  • James Dolezal

    (University of Chicago)

  • Sara Kochanny

    (University of Chicago)

  • Jefree Schulte

    (University of Chicago)

  • Heather Chen

    (University of Chicago)

  • Lara Heij

    (University Hospital RWTH Aachen
    University Hospital RWTH Aachen)

  • Dezheng Huo

    (University of Chicago
    University of Chicago Comprehensive Cancer Center)

  • Rita Nanda

    (University of Chicago
    University of Chicago Comprehensive Cancer Center)

  • Olufunmilayo I. Olopade

    (University of Chicago
    University of Chicago Comprehensive Cancer Center)

  • Jakob N. Kather

    (University Hospital RWTH Aachen
    University of Leeds
    University Hospital Heidelberg)

  • Nicole Cipriani

    (University of Chicago
    University of Chicago Comprehensive Cancer Center)

  • Robert L. Grossman

    (University of Chicago
    University of Chicago Comprehensive Cancer Center)

  • Alexander T. Pearson

    (University of Chicago
    University of Chicago Comprehensive Cancer Center)

Abstract

The Cancer Genome Atlas (TCGA) is one of the largest biorepositories of digital histology. Deep learning (DL) models have been trained on TCGA to predict numerous features directly from histology, including survival, gene expression patterns, and driver mutations. However, we demonstrate that these features vary substantially across tissue submitting sites in TCGA for over 3,000 patients with six cancer subtypes. Additionally, we show that histologic image differences between submitting sites can easily be identified with DL. Site detection remains possible despite commonly used color normalization and augmentation methods, and we quantify the image characteristics constituting this site-specific digital histology signature. We demonstrate that these site-specific signatures lead to biased accuracy for prediction of features including survival, genomic mutations, and tumor stage. Furthermore, ethnicity can also be inferred from site-specific signatures, which must be accounted for to ensure equitable application of DL. These site-specific signatures can lead to overoptimistic estimates of model performance, and we propose a quadratic programming method that abrogates this bias by ensuring models are not trained and validated on samples from the same site.

Suggested Citation

  • Frederick M. Howard & James Dolezal & Sara Kochanny & Jefree Schulte & Heather Chen & Lara Heij & Dezheng Huo & Rita Nanda & Olufunmilayo I. Olopade & Jakob N. Kather & Nicole Cipriani & Robert L. Gro, 2021. "The impact of site-specific digital histology signatures on deep learning model accuracy and bias," Nature Communications, Nature, vol. 12(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-24698-1
    DOI: 10.1038/s41467-021-24698-1
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    Cited by:

    1. MarĂ­a Agustina Ricci Lara & Rodrigo Echeveste & Enzo Ferrante, 2022. "Addressing fairness in artificial intelligence for medical imaging," Nature Communications, Nature, vol. 13(1), pages 1-6, December.
    2. Omar S. M. El Nahhas & Chiara M. L. Loeffler & Zunamys I. Carrero & Marko Treeck & Fiona R. Kolbinger & Katherine J. Hewitt & Hannah S. Muti & Mara Graziani & Qinghe Zeng & Julien Calderaro & Nadina O, 2024. "Regression-based Deep-Learning predicts molecular biomarkers from pathology slides," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
    3. Adalberto Claudio Quiros & Nicolas Coudray & Anna Yeaton & Xinyu Yang & Bojing Liu & Hortense Le & Luis Chiriboga & Afreen Karimkhan & Navneet Narula & David A. Moore & Christopher Y. Park & Harvey Pa, 2024. "Mapping the landscape of histomorphological cancer phenotypes using self-supervised learning on unannotated pathology slides," Nature Communications, Nature, vol. 15(1), pages 1-24, December.

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