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

Journal: Nature communications
PMID:

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.

Authors

  • Jay Jasti
    Lyda Hill Department of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, Texas.
  • Hua Zhong
    Department of Population Health, NYU Grossman School of Medicine, New York, NY, USA.
  • Vandana Panwar
    Department of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas.
  • Vipul Jarmale
    Lyda Hill Department of Bioinformatics, The University of Texas Southwestern Medical Center, Dallas, USA.
  • Jeffrey Miyata
    Kidney Cancer Program, Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Deyssy Carrillo
    Kidney Cancer Program, Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Alana Christie
    Kidney Cancer Program, Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, Texas.
  • Dinesh Rakheja
    2 University of Texas Southwestern Medical Center , Dallas, Texas.
  • Zora Modrusan
    Department of Molecular Biology, Genentech, Inc., South San Francisco, California.
  • Edward Ernest Kadel
    Translational Medicine Oncology, Genentech, South San Francisco, CA, USA.
  • Niha Beig
    Case Western Reserve University, 10900 Euclid Avenue, Cleveland, OH 44106, United States.
  • Mahrukh Huseni
    Translational Medicine Oncology, Genentech, South San Francisco, CA, USA.
  • James Brugarolas
    Kidney Cancer Program, Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, Texas.
  • Payal Kapur
    Department of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas.
  • Satwik Rajaram
    Lyda Hill Department of Bioinformatics, The University of Texas Southwestern Medical Center, Dallas, USA. satwik.rajaram@utsouthwestern.edu.