mlsanityData to 7 Oct 2026

Harnessing Adversarial Distillation to Customise Debiased, Disease-Specific Pathology Foundation Models for Breast Cancer

arXiv 2608.01356 ↗First posted 2 Aug 2026cs.CVcited by 0

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Abstract (arXiv)

Pathology foundation models (PFMs) provide strong tissue representations and have become central to digital pathology. However, deployment in disease-specific settings is limited by 1) the high computational cost of billion-parameter PFMs and 2) distribution mismatch and non-biological bias inherited from pan-cancer, multi-centre pre-training, including site-specific signatures and imbalanced disease prevalence. These factors can encourage shortcut learning and under-emphasise subtle morphology required for reliable modelling of a specific cancer type. We present SmartStu (a Smart Student), a framework to customise compact, breast-cancer-specific PFMs via distillation whilst mitigating confounding. SmartStu distils representations from multiple teacher PFMs into a lightweight student backbone. Crucially, we introduce adversarial distillation that leverages a dedicated noise model trained to predict nuisance, edge-dominated cues on the distillation set. Using this noise model as a counterexample, the adversarial objective encourages the student to recognise, yet suppress, features predictive of nuisance targets. We further incorporate multi-teacher ensemble distillation and an auxiliary self-supervised objective with artefact injection. We validate SmartStu on three external cohorts (Yale HER2, SLN-Breast, and BRACS) with multiple tiny backbones. SmartStu yields breast-cancer-specific PFMs that are over 30× smaller than general PFMs whilst largely preserving, and sometimes improving, downstream performance measured by balanced accuracy (bAcc) and AUC. Code is available at https://github.com/zwchen03/advDistall.

Key facts. No citing papers in the map yet (data through 7 Oct 2026). Builds on 16 of its 29 references that are in the map. First posted on arXiv 2 Aug 2026.

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16 of 29 references.

References · 16

  1. 2023DINOv2: Learning Robust Visual Features without Supervisioncited by 7,764
  2. 2021Emerging Properties in Self-Supervised Vision Transformerscited by 6,893
  3. 2015Domain-Adversarial Training of Neural Networkscited by 3,023
  4. 2020Supervised Contrastive Learningcited by 2,803
  5. 2021iBOT: Image BERT Pre-Training with Online Tokenizercited by 891
  6. 2020Eigen-CAM: Class Activation Map using Principal Componentscited by 188
  7. 2024Virchow2: Scaling Self-Supervised Mixed Magnification Models in Pathologycited by 144
  8. 2021BRACS: A Dataset for BReAst Carcinoma Subtyping in H&E Histology Imagescited by 130
  9. 2024Phikon-v2, A large and public feature extractor for biomarker predictioncited by 67
  10. 2024A Multimodal Knowledge-enhanced Whole-slide Pathology Foundation Modelcited by 59
  11. 2025Accelerating Data Processing and Benchmarking of AI Models for Pathologycited by 58
  12. 2025Distilling foundation models for robust and efficient models in digital pathologycited by 33
4 more
  1. 2023Domain Generalization in Computational Pathology: Survey and Guidelinescited by 29
  2. 2024Do Histopathological Foundation Models Eliminate Batch Effects? A Comparative Studycited by 17
  3. 2025A Survey on Computational Pathology Foundation Models: Datasets, Adaptation Strategies, and Evaluation Taskscited by 15
  4. 2025A Survey of Pathology Foundation Model: Progress and Future Directionscited by 14

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