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CorePath: A Breast-Specialized Pathology Foundation Model for Core Needle Biopsy Diagnosis and Risk-Controlled Report Generation

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Do you know Ting Yin?You can claim authorship or link another user.Do you know Danning Li?You can claim authorship or link another user.Do you know Chen Shu?You can claim authorship or link another user.Do you know Xiaoxia Yao?You can claim authorship or link another user.Do you know Boyu Fu?You can claim authorship or link another user.Do you know Yujing Chang?You can claim authorship or link another user.Do you know Tianyu Shi?You can claim authorship or link another user.Do you know Mengna Feng?You can claim authorship or link another user.Do you know Jie Chen?You can claim authorship or link another user.Do you know Jing Fu?You can claim authorship or link another user.Do you know Xiuli Xiao?You can claim authorship or link another user.Do you know Tianlin Li?You can claim authorship or link another user.Do you know Mumin Shao?You can claim authorship or link another user.Do you know Jiaxin Bi?You can claim authorship or link another user.Do you know Wenchuan Zhang?You can claim authorship or link another user.Do you know Xiaoyan Wu?You can claim authorship or link another user.Do you know Xiao Han?You can claim authorship or link another user.Do you know Zhang Zhang?You can claim authorship or link another user.Do you know Yuhao Yi?You can claim authorship or link another user.Do you know Hong Bu?You can claim authorship or link another user.

Abstract

Breast core needle biopsy (CNB) is central to breast cancer diagnosis yet remains challenging because limited tissue sampling, lesion heterogeneity, and subtle morphologic overlap can obscure subtype distinctions. We developed CorePath, a breast-specialized multimodal pathology foundation model fine-tuned from PRISM using 7901 paired CNB whole-slide images and diagnostic reports from two centers. Evaluated across six CNB cohorts and two public breast pathology benchmarks without task-specific retraining, CorePath consistently outperformed PRISM across cancer detection, invasion assessment, and histological subtyping. It achieved weighted area under the receiver operating characteristic curves (AUCs) of 0.9526-0.9735 for five-class CNB histological subtyping across private centers. On public benchmarks, CorePath outperformed leading pathology foundation models, achieving the highest weighted AUCs of 0.7780 for BCNB invasive carcinoma subtyping, 0.8178 for BRACS lesion stratification, and 0.8252 for BRACS fine-grained classification. In report generation, CorePath reduced the overall non-breast hallucinations from 30.1% to 2.8%, demonstrating improved domain fidelity after breast-specific adaptation. CorePath-CRG further combined conformal subtype-confidence gating with Learn-Then-Test risk control to enable selective report release, subtype-level fallback, and deferral. CorePath-CRG achieved zero non-breast hallucinations among released outputs and showed the strongest overall performance in pathologist-validated LLM-based Evaluation Scores and quantitative report-generation metrics across most centers. These results demonstrate that domain-specialized foundation models with statistical risk control offer a promising approach for accurate breast CNB diagnosis and reliable report generation.

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The code will be made publicly available upon publication