Demonstrates improved molecular subtyping in breast cancer, suggesting enhanced treatment planning.
Accurate molecular subtyping of breast cancer is essential for treatment planning, yet computational methods face challenges from class imbalance and variable-quality histopathology features. We propose a multi-modal framework that integrates histopathology image features with genomic expression data through prototype-based contrastive alignment and clinical guideline-aware attention. The framework computes class-conditional prototypes in each modality’s latent space and aligns them via a bidirectional contrastive loss, decoupling representation learning from sample-level pairing requirements. A clinical attention mechanism encodes established breast cancer biomarker profiles as structured prior knowledge within the fusion architecture. Evaluated on 916 patients from TCGA-BRCA with PAM50 molecular labels using CLAM histopathology features and RNA-Seq expression data, the framework achieves macro-averaged F1 of 0.843 ± 0.012 in 5-fold cross-validation. Clinical attention is the most impactful component (contributing + 5.8% macro F1 over uniform fusion), followed by genomic-supervised feature learning via knowledge distillation (+ 2.1%). An exploratory Histogenomic Discordance Score measuring cross-modal prediction disagreement shows directionally consistent but non-significant association with disease-free survival (HR = 1.91, p = 0.25). These results demonstrate that structured clinical knowledge injection through guideline-aware attention provides measurable improvements in multi-modal breast cancer subtyping under realistic feature quality constraints.
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Guan et al. (2026) studied this question.
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