Understanding Synergistic Interactions among Pathology Foundation Models via Adaptive Fusion
- URL: http://arxiv.org/abs/2608.01370v1
- Date: Sun, 02 Aug 2026 16:44:45 GMT
- Title: Understanding Synergistic Interactions among Pathology Foundation Models via Adaptive Fusion
- Abstract summary: Pathology foundation models (PFMs) provide strong tile-level representations via self-supervised pre-training on large-scale pathology images.<n>We present AdaFusion, a lightweight adaptive fusion framework that integrates complementary signals from multiple frozen PFMs.<n>AdaFusion consistently outperforms individual PFMs and other fusion baselines, while providing interpretable tissue visualisation.
- Score: 49.550545038402184
- License: http://arxiv.org/licenses/nonexclusive-distrib/1.0/
- Abstract: Pathology foundation models (PFMs) provide strong tile-level representations via self-supervised pre-training on large-scale pathology images. Yet, PFMs are developed under diverse and often opaque data, architecture, and objective choices, inducing latent representational biases that limit robustness and obscure what each model specialises in. We present AdaFusion, a lightweight adaptive fusion framework that integrates complementary signals from multiple frozen PFMs through (1) low-dimensional feature compression and (2) a sample-conditioned gating module that reweights model-wise (and optionally channel-wise) contributions. Beyond improving predictive accuracy, AdaFusion provides contribution-driven interpretation that offers evidence consistent with model-specific preferences and synergistic interactions across tissue phenotypes. We evaluate AdaFusion on three public benchmarks spanning treatment response prediction, prostate cancer grading, and spatial gene expression inference. AdaFusion consistently outperforms individual PFMs and other fusion baselines, while providing interpretable tissue visualisation which aligns model preferences with morphological patterns. Code is available at: https://github.com/xyx-98/PathoOracle.
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