# AdaFusion: Prompt-Guided Inference with Adaptive Fusion of Pathology Foundation Models

arXiv: https://arxiv.org/abs/2508.05084 · HTML: https://mlsanity.com/paper/2508.05084/

## Key facts

- No citing papers in the map yet (data through 14 Oct 2026).
- Builds on 11 of its 23 references that are in the map.
- First posted on arXiv 7 Aug 2025.

## Builds on (most cited first, 11 of 11)

- [DINOv2: Learning Robust Visual Features without Supervision](https://mlsanity.com/paper/2304.07193/) (2023)
- [Attention-based Deep Multiple Instance Learning](https://mlsanity.com/paper/1802.04712/) (2018)
- [Data Efficient and Weakly Supervised Computational Pathology on Whole Slide Images](https://mlsanity.com/paper/2004.09666/) (2020)
- [Dual-stream Multiple Instance Learning Network for Whole Slide Image Classification with Self-supervised Contrastive Learning](https://mlsanity.com/paper/2011.08939/) (2020)
- [Virchow2: Scaling Self-Supervised Mixed Magnification Models in Pathology](https://mlsanity.com/paper/2408.00738/) (2024)
- [HEST-1k: A Dataset for Spatial Transcriptomics and Histology Image Analysis](https://mlsanity.com/paper/2406.16192/) (2024)
- [Phikon-v2, A large and public feature extractor for biomarker prediction](https://mlsanity.com/paper/2409.09173/) (2024)
- [Accelerating Data Processing and Benchmarking of AI Models for Pathology](https://mlsanity.com/paper/2502.06750/) (2025)
- [Self-Supervision Closes the Gap Between Weak and Strong Supervision in Histology](https://mlsanity.com/paper/2012.03583/) (2020)
- [Current Pathology Foundation Models are unrobust to Medical Center Differences](https://mlsanity.com/paper/2501.18055/) (2025)
- [Unsupervised Foundation Model-Agnostic Slide-Level Representation Learning](https://mlsanity.com/paper/2411.13623/) (2024)

## Abstract (arXiv)

Pathology foundation models (PFMs) have demonstrated strong representational capabilities through self-supervised pre-training on large-scale, unannotated histopathology image datasets. However, their diverse yet opaque pretraining contexts, shaped by both data-related and structural/training factors, introduce latent biases that hinder generalisability and transparency in downstream applications. In this paper, we propose AdaFusion, a novel prompt-guided inference framework that, to our knowledge, is among the very first to dynamically integrate complementary knowledge from multiple PFMs. Our method compresses and aligns tile-level features from diverse models and employs a lightweight attention mechanism to adaptively fuse them based on tissue phenotype context. We evaluate AdaFusion on three real-world benchmarks spanning treatment response prediction, tumour grading, and spatial gene expression inference. Our approach consistently surpasses individual PFMs across both classification and regression tasks, while offering interpretable insights into each model's biosemantic specialisation. These results highlight AdaFusion's ability to bridge heterogeneous PFMs, achieving both enhanced performance and interpretability of model-specific inductive biases.
