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

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.

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Publication Details

Journal
Nature Communications
Published
2025-03-17
DOI
https://doi.org/10.1038/s41467-025-57717-6
Citations
21
Primary Topic
Renal cell carcinoma treatment
Type
article
Field-Weighted Citation Impact
31.89

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article

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

Deyssy Carrillo, Jeffrey Miyata, Vipul Jarmale, Dinesh Rakheja et al.
21 citations
Nature Communications
Renal cell carcinoma treatment
31.89
article

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

Deyssy Carrillo, Jeffrey Miyata, Vipul Jarmale, Dinesh Rakheja, James Brugarolas, Niha Beig, Satwik Rajaram, Edward E. Kadel, Jay Jasti, Mahrukh Huseni, Payal Kapur, Hua Zhong, Vandana Panwar, Alana Christie, Zora Modrusan
article en
21 citations

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.

Nature CommunicationsVol. 16(1)
Southwestern Medical Center (US), Genomic Health (United States) (US), The University of Texas Southwestern Medical Center (US)
U.S. Department of Defense, Cancer Prevention and Research Institute of Texas, National Institutes of Health
Good health and well-being
Openalex Percentile: Top 0%
Renal cell carcinoma treatment
31.89
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