Research
Cellular-Communication-Level Interpretability for Pathology Foundation Models via Graph Distillation on Microenvironment
arXiv:2609.26073v1 Announce Type: new Abstract: Pathology foundation models (PFMs) provide strong tile-level representations but remain difficult to interpret at the cellular and microenvironmental sc
arXiv:2609.26073v1 Announce Type: new Abstract: Pathology foundation models (PFMs) provide strong tile-level representations but remain difficult to interpret at the cellular and microenvironmental scales that underpin clinical reasoning. We introduce Graph-Interpreter (G-Interp), a graph-distillation framework that equips a frozen PFM teacher with a cellular-communication-level "plug-in" interpreter, without modifying the teacher. For each tile, we segment cells as graph nodes and construct a microenvironment graph based on spatial adjacency. Graph neural network (GNN) students distil the PFM embedding, whilst learning attention-based message passing that yields node- and edge-level importances. We interpret these importances as cell-cell communication evidence, providing fine-grained explanations of how PFMs encode microenvironmental context. To stabilise distillation when graph abstraction is imperfect, we employ a lightweight auxiliary student to supply complementary visual cues and condition graph message passing, while keeping the primary interpretability signal graph-derived. We evaluate explanation faithfulness by mapping graph-selected evidence back to the image using instance masks and measuring teacher sensitivity under targeted vs non-target occlusions. Across multiple histopathology tasks, G-Interp produces highly scalable, microenvironment-aware explanations, while maintaining competitive predictive performance.
Source: arXiv cs.CV | 2026-09-23