Evidence map›Paper›PMID 42421885›Full record

ArticleProceedings of machine learning research2026

Comparing Computational Pathology Foundation Models using Representational Similarity Analysis.

Vaibhav Mishra, William Lotter

Abstract read
In one paragraph

Article in Proceedings of machine learning research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
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  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Vaibhav MishraDana-Farber Cancer Institute.
William LotterDana-Farber Cancer Institute, Brigham and Women's Hospital, & Harvard Medical School.

Funding

Computational methods for multiplex image analysis of the tumor microenvironmentR01LM014775 · NLM · DANA-FARBER CANCER INST · PI LOTTER, WILLIAM EDWARD · 2025 to 2025
$1.6M
Improving prognosis prediction and therapy selection for cutaneous squamous cell carcinomas using artificial intelligenceR21EB035247 · NIBIB · DANA-FARBER CANCER INST · PI LOTTER, WILLIAM EDWARD · 2024 to 2024
$693k
NIBIB NIH HHS R21 EB035247NLM NIH HHS R01 LM014775
6 · The paper itself

Abstract

Foundation models are increasingly developed in computational pathology (CPath) given their promise in facilitating many downstream tasks. While recent studies have evaluated task performance across models, less is known about the structure and variability of their learned representations. Here, we systematically analyze the representational spaces of six CPath foundation models using techniques popularized in computational neuroscience. The models analyzed span vision-language contrastive learning (CONCH, PLIP, KEEP) and self-distillation (UNI (v2), Virchow (v2), Prov-GigaPath) approaches. Through representational similarity analysis using H&E image patches from TCGA, we find that UNI2 and Virchow2 have the most distinct representational structures, whereas Prov-Gigapath has the highest average similarity across models. Having the same training paradigm (vision-only vs. vision-language) did not guarantee higher representational similarity. The representations of all models showed a high slide-dependence, but relatively low disease-dependence. Stain normalization decreased slide-dependence for all models by a range of 5.5% (CONCH) to 20.5% (PLIP). In terms of intrinsic dimensionality, vision-language models demonstrated relatively compact representations, compared to the more distributed representations of vision-only models. These findings highlight opportunities to improve robustness to slide-specific features, inform model ensembling strategies, and provide insights into how training paradigms shape model representations. Our framework is extendable across medical imaging domains, where probing the internal representations of foundation models can support their effective development and deployment.

Indexed as

computational pathologyfoundation modelsrepresentation analysisrobustness

Identifiers

PMID42421885
PMCPMC13345687

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.