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Histopathology based AI model predicts anti-angiogenic therapy response in renal cancer clinical trial

Author

Listed:
  • Jay Jasti

    (University of Texas Southwestern Medical Center)

  • Hua Zhong

    (University of Texas Southwestern Medical Center
    University of Texas Southwestern Medical Center)

  • Vandana Panwar

    (University of Texas Southwestern Medical Center)

  • Vipul Jarmale

    (University of Texas Southwestern Medical Center)

  • Jeffrey Miyata

    (University of Texas Southwestern Medical Center)

  • Deyssy Carrillo

    (University of Texas Southwestern Medical Center)

  • Alana Christie

    (University of Texas Southwestern Medical Center
    The University of Texas Southwestern Medical Center)

  • Dinesh Rakheja

    (University of Texas Southwestern Medical Center)

  • Zora Modrusan

    (Genentech)

  • Edward Ernest Kadel

    (Genentech
    Genentech)

  • Niha Beig

    (Genentech)

  • Mahrukh Huseni

    (Genentech)

  • James Brugarolas

    (University of Texas Southwestern Medical Center
    University of Texas Southwestern Medical Center)

  • Payal Kapur

    (University of Texas Southwestern Medical Center
    University of Texas Southwestern Medical Center)

  • Satwik Rajaram

    (University of Texas Southwestern Medical Center
    University of Texas Southwestern Medical Center
    University of Texas Southwestern Medical Center)

Abstract

Anti-angiogenic (AA) therapy is a cornerstone of metastatic clear cell renal cell carcinoma (ccRCC) treatment, but not everyone responds, and predictive biomarkers are lacking. CD31, a marker of vasculature, is insufficient, and the Angioscore, an RNA-based angiogenesis quantification method, is costly, associated with delays, difficult to standardize, and does not account for tumor heterogeneity. Here, we developed an interpretable deep learning (DL) model that predicts the Angioscore directly from ubiquitous histopathology slides yielding a visual vascular network (H&E DL Angio). H&E DL Angio achieves a strong correlation with the Angioscore across multiple cohorts (spearman correlations of 0.77 and 0.73). Using this approach, we found that angiogenesis inversely correlates with grade and stage and is associated with driver mutation status. Importantly, DL Angio expediently predicts AA response in both a real-world and IMmotion150 trial cohorts, out-performing CD31, and closely approximating the Angioscore (c-index 0.66 vs 0.67) at a fraction of the cost.

Suggested Citation

  • Jay Jasti & Hua Zhong & Vandana Panwar & Vipul Jarmale & Jeffrey Miyata & Deyssy Carrillo & Alana Christie & Dinesh Rakheja & Zora Modrusan & Edward Ernest Kadel & Niha Beig & Mahrukh Huseni & James B, 2025. "Histopathology based AI model predicts anti-angiogenic therapy response in renal cancer clinical trial," Nature Communications, Nature, vol. 16(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-57717-6
    DOI: 10.1038/s41467-025-57717-6
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    References listed on IDEAS

    as
    1. Benoît Schmauch & Alberto Romagnoni & Elodie Pronier & Charlie Saillard & Pascale Maillé & Julien Calderaro & Aurélie Kamoun & Meriem Sefta & Sylvain Toldo & Mikhail Zaslavskiy & Thomas Clozel & Matah, 2020. "A deep learning model to predict RNA-Seq expression of tumours from whole slide images," Nature Communications, Nature, vol. 11(1), pages 1-15, December.
    2. Francesco Cisternino & Sara Ometto & Soumick Chatterjee & Edoardo Giacopuzzi & Adam P. Levine & Craig A. Glastonbury, 2024. "Self-supervised learning for characterising histomorphological diversity and spatial RNA expression prediction across 23 human tissue types," Nature Communications, Nature, vol. 15(1), pages 1-16, December.
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