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Single GPU Task Adaptation of Pathology Foundation Models for Whole Slide Image Analysis
by
Kumar, Neeraj
, Jie-Fu, Chen
, Goldgof, Gregory M
, Singi, Siddharth
, Campanella, Gabriele
, Nanda, Swaraj
, Vanderbilt, Chad
, Benhamida, Jamal
, Kim, David
, Momeni-Boroujeni, Amir
in
Adaptation
/ Attention
/ Image analysis
/ Labels
/ Mutation
/ Pathology
2025
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Single GPU Task Adaptation of Pathology Foundation Models for Whole Slide Image Analysis
by
Kumar, Neeraj
, Jie-Fu, Chen
, Goldgof, Gregory M
, Singi, Siddharth
, Campanella, Gabriele
, Nanda, Swaraj
, Vanderbilt, Chad
, Benhamida, Jamal
, Kim, David
, Momeni-Boroujeni, Amir
in
Adaptation
/ Attention
/ Image analysis
/ Labels
/ Mutation
/ Pathology
2025
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Do you wish to request the book?
Single GPU Task Adaptation of Pathology Foundation Models for Whole Slide Image Analysis
by
Kumar, Neeraj
, Jie-Fu, Chen
, Goldgof, Gregory M
, Singi, Siddharth
, Campanella, Gabriele
, Nanda, Swaraj
, Vanderbilt, Chad
, Benhamida, Jamal
, Kim, David
, Momeni-Boroujeni, Amir
in
Adaptation
/ Attention
/ Image analysis
/ Labels
/ Mutation
/ Pathology
2025
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Single GPU Task Adaptation of Pathology Foundation Models for Whole Slide Image Analysis
Paper
Single GPU Task Adaptation of Pathology Foundation Models for Whole Slide Image Analysis
2025
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Overview
Pathology foundation models (PFMs) have emerged as powerful tools for analyzing whole slide images (WSIs). However, adapting these pretrained PFMs for specific clinical tasks presents considerable challenges, primarily due to the availability of only weak (WSI-level) labels for gigapixel images, necessitating multiple instance learning (MIL) paradigm for effective WSI analysis. This paper proposes a novel approach for single-GPU Task Adaptation of PFMs (TAPFM) that uses vision transformer () attention for MIL aggregation while optimizing both for feature representations and attention weights. The proposed approach maintains separate computational graphs for MIL aggregator and the PFM to create stable training dynamics that align with downstream task objectives during end-to-end adaptation. Evaluated on mutation prediction tasks for bladder cancer and lung adenocarcinoma across institutional and TCGA cohorts, TAPFM consistently outperforms conventional approaches, with H-Optimus-0 (TAPFM) outperforming the benchmarks. TAPFM effectively handles multi-label classification of actionable mutations as well. Thus, TAPFM makes adaptation of powerful pre-trained PFMs practical on standard hardware for various clinical applications.
Publisher
Cornell University Library, arXiv.org
Subject
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