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A Comprehensive Benchmark of Histopathology Foundation Models for Kidney Digital Pathology Images

Harishwar Reddy Kasireddy
Patricio S. La Rosa
Akshita Gupta
Anindya S. Paul
Jamie L. Fermin
William L. Clapp
Meryl A. Waldman
Tarek M. El-Ashkar
Sanjay Jain
Luis Rodrigues
Kuang Yu Jen
Avi Z. Rosenberg
Michael T. Eadon
Jeffrey B. Hodgin
Pinaki Sarder
Main:22 Pages
10 Figures
Bibliography:5 Pages
14 Tables
Appendix:4 Pages
Abstract

Histopathology foundation models (HFMs), pretrained on large-scale cancer datasets, have advanced computational pathology. However, their applicability to non-cancerous chronic kidney disease remains underexplored, despite coexistence of renal pathology with malignancies such as renal cell and urothelial carcinoma. We systematically evaluate 11 publicly available HFMs across 11 kidney-specific downstream tasks spanning multiple stains (PAS, H&E, PASM, and IHC), spatial scales (tile and slide-level), task types (classification, regression, and copy detection), and clinical objectives, including detection, diagnosis, and prognosis. Tile-level performance is assessed using repeated stratified group cross-validation, while slide-level tasks are evaluated using repeated nested stratified cross-validation. Statistical significance is examined using Friedman test followed by pairwise Wilcoxon signed-rank testing with Holm-Bonferroni correction and compact letter display visualization. To promote reproducibility, we release an open-source Python package, kidney-hfm-eval, available atthis https URL, that reproduces the evaluation pipelines. Results show moderate to strong performance on tasks driven by coarse meso-scale renal morphology, including diagnostic classification and detection of prominent structural alterations. In contrast, performance consistently declines for tasks requiring fine-grained microstructural discrimination, complex biological phenotypes, or slide-level prognostic inference, largely independent of stain type. Overall, current HFMs appear to encode predominantly static meso-scale representations and may have limited capacity to capture subtle renal pathology or prognosis-related signals. Our results highlight the need for kidney-specific, multi-stain, and multimodal foundation models to support clinically reliable decision-making in nephrology.

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