Information-driven Fusion of Pathology Foundation Models for Enhanced Disease Characterization

TL;DR

This study introduces an information-driven fusion method for combining multiple pathology foundation models, improving cancer grading and staging accuracy while enhancing interpretability across diverse cancer types.

Contribution

It proposes a correlation-guided intelligent fusion strategy for pathology models, systematically evaluating its effectiveness for cancer classification tasks.

Findings

Fusion improves classification accuracy over single models.

Embedding spaces show substantial alignment but also complementarity.

Attention maps focus on tumor regions, reducing benign region distraction.

Abstract

Foundation models (FMs) have demonstrated strong performance across diverse pathology tasks. While there are similarities in the pre-training objectives of FMs, there is still limited understanding of their complementarity, redundancy in embedding spaces, or biological interpretation of features. In this study, we propose an information-driven, intelligent fusion strategy for integrating multiple pathology FMs into a unified representation and systematically evaluate its performance for cancer grading and staging across three distinct diseases. Diagnostic H&E whole-slide images from kidney (519 slides), prostate (490 slides), and rectal (200 slides) cancers were dichotomized into low versus high grade or stage. Both tile-level FMs (Conch v1.5, MUSK, Virchow2, H-Optimus1, Prov-Gigapath) and slide-level FMs (TITAN, CHIEF, MADELEINE) were considered to train downstream classifiers. We then evaluated three FM fusion schemes at both tile and slide levels: majority-vote ensembling, naive feature concatenation, and intelligent fusion based on correlation-guided pruning of redundant features. Under patient-stratified cross-validation with hold-out testing, intelligent fusion of tile-level embeddings yielded consistent gains in classification performance across all three cancers compared with the best single FMs and naive fusion. Global similarity metrics revealed substantial alignment of FM embedding spaces, contrasted by lower local neighborhood agreement, indicating complementary fine-grained information across FMs. Attention maps showed that intelligent fusion yielded concentrated attention on tumor regions while reducing spurious focus on benign regions. Our findings suggest that intelligent, correlation-guided fusion of pathology FMs can yield compact, task-tailored representations that enhance both predictive performance and interpretability in downstream computational pathology tasks.