Knowledge-guided adaptation of pathology foundation models effectively improves cross-domain generalization and demographic fairness

Foundation models in computational pathology suffer from site-specific and demographic biases, which compromise their generalizability and fairness. We introduce FLEX, a framework that employs a task-specific information bottleneck, guided by visual and textual domain knowledge, to disentangle robust pathological features from these artifacts. Using three large cohorts (The Cancer Genome Atlas, Clinical Proteomic Tumor Analysis Consortium, and an in-house dataset) across 16 clinical tasks, totaling over 9,900 slides, we demonstrate that FLEX achieves superior zero-shot generalization to unseen external cohorts, significantly outperforming baselines and narrowing the performance gap between seen and unseen domains. A comprehensive fairness analysis confirms that FLEX also effectively mitigates disparities across demographic groups. Furthermore, its versatility and scalability are proven through compatibility with various foundation models and multiple-instance learning architectures. Our work establishes FLEX as a promising solution for developing more generalizable and equitable pathology AI for diverse clinical settings.

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Publication Details

Journal
Nature Communications
Published
2025-12-12
DOI
https://doi.org/10.1038/s41467-025-66300-y
Citations
2
Primary Topic
AI in cancer detection
Type
article
Field-Weighted Citation Impact
4.96
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article

Knowledge-guided adaptation of pathology foundation models effectively improves cross-domain generalization and demographic fairness

Yuguang Fu, Zhengyu Zhang, Lequan Yu, Yuming Jiang et al.
2 citations
Nature Communications
AI in cancer detection
4.96
article

Knowledge-guided adaptation of pathology foundation models effectively improves cross-domain generalization and demographic fairness

Yuguang Fu, Zhengyu Zhang, Lequan Yu, Yuming Jiang, Feng Wu, Shujun Wang, Li Liang, Yanyan Huang, Yihang Chen, Weiqin Zhao
article en
2 citations

Abstract

Foundation models in computational pathology suffer from site-specific and demographic biases, which compromise their generalizability and fairness. We introduce FLEX, a framework that employs a task-specific information bottleneck, guided by visual and textual domain knowledge, to disentangle robust pathological features from these artifacts. Using three large cohorts (The Cancer Genome Atlas, Clinical Proteomic Tumor Analysis Consortium, and an in-house dataset) across 16 clinical tasks, totaling over 9,900 slides, we demonstrate that FLEX achieves superior zero-shot generalization to unseen external cohorts, significantly outperforming baselines and narrowing the performance gap between seen and unseen domains. A comprehensive fairness analysis confirms that FLEX also effectively mitigates disparities across demographic groups. Furthermore, its versatility and scalability are proven through compatibility with various foundation models and multiple-instance learning architectures. Our work establishes FLEX as a promising solution for developing more generalizable and equitable pathology AI for diverse clinical settings.

Nature CommunicationsVol. 16(1)
Hong Kong Polytechnic University (HK), Chongqing University (CN), Chinese University of Hong Kong (HK), Key Laboratory of Guangdong Province (CN), Nanfang Hospital (CN), Wake Forest University (US), Southern Medical University (CN), Lanzhou University (CN), University of Hong Kong (HK)
Openalex Percentile: Top 4%
AI in cancer detection
4.96
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