Yongxin Guo , Ziyu Su , Onur C. Koyun , Hao Lu , Robert Wesolowski , Gary Tozbikian , M. Khalid Khan Niazi , Metin N. Gurcan
{"title":"BPMambaMIL:一种生物启发原型引导的多实例学习,用于组织病理学中oncotype DX风险评估。","authors":"Yongxin Guo , Ziyu Su , Onur C. Koyun , Hao Lu , Robert Wesolowski , Gary Tozbikian , M. Khalid Khan Niazi , Metin N. Gurcan","doi":"10.1016/j.cmpb.2025.109039","DOIUrl":null,"url":null,"abstract":"<div><div>Breast cancer remains one of the most prevalent malignancies among women, with hormone receptor-positive (HR+)/human epidermal growth factor receptor 2-negative (HER2–) breast cancers constituting a majority, with treatment decisions often guided by genomic assays such as the 21-gene recurrence score assay, Oncotype DX. Although Oncotype DX provides critical prognostic and predictive insights, its high cost and limited accessibility create substantial barriers, especially for patients with constrained financial resources. To reduce the test cost, we aim to leverage H&E-stained whole slide images (WSIs) to predict Oncotype DX risk. Since WSIs are extremely large and contain redundant information, directly processing them is both computationally expensive and prone to errors. To address these limitations, we introduce a bio-inspired prototype-guided model (BPMambaMIL), a novel weakly supervised learning framework that integrates the Mamba mechanism with prototypical guidance to predict Oncotype DX score intervals directly from pathology images. Our model was evaluated on an in-house dataset with clinical Oncotype DX scores, where it achieved an AUC of 0.839, a 5.61 % improvement over the baseline model (MambaMIL), and demonstrated robust predictive performance, particularly in identifying high-risk score ranges (accuracy: 0.714 vs 0.419). Further assessments on two public breast cancer pathology image datasets using six state-of-the-art models underscored BPMambaMIL’s generalizability on research-based ODX scores and binary tumor classification tasks. By evaluating various clinical scenarios, the proposed method not only enhances the accuracy of breast cancer recurrence risk predictions but also offers a cost-effective alternative to genomic assays, thus improving clinical outcomes.</div></div>","PeriodicalId":10624,"journal":{"name":"Computer methods and programs in biomedicine","volume":"272 ","pages":"Article 109039"},"PeriodicalIF":4.8000,"publicationDate":"2025-08-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"BPMambaMIL: A bio-inspired prototype-guided multiple instance learning for oncotype DX risk assessment in histopathology\",\"authors\":\"Yongxin Guo , Ziyu Su , Onur C. Koyun , Hao Lu , Robert Wesolowski , Gary Tozbikian , M. Khalid Khan Niazi , Metin N. Gurcan\",\"doi\":\"10.1016/j.cmpb.2025.109039\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Breast cancer remains one of the most prevalent malignancies among women, with hormone receptor-positive (HR+)/human epidermal growth factor receptor 2-negative (HER2–) breast cancers constituting a majority, with treatment decisions often guided by genomic assays such as the 21-gene recurrence score assay, Oncotype DX. Although Oncotype DX provides critical prognostic and predictive insights, its high cost and limited accessibility create substantial barriers, especially for patients with constrained financial resources. To reduce the test cost, we aim to leverage H&E-stained whole slide images (WSIs) to predict Oncotype DX risk. Since WSIs are extremely large and contain redundant information, directly processing them is both computationally expensive and prone to errors. To address these limitations, we introduce a bio-inspired prototype-guided model (BPMambaMIL), a novel weakly supervised learning framework that integrates the Mamba mechanism with prototypical guidance to predict Oncotype DX score intervals directly from pathology images. Our model was evaluated on an in-house dataset with clinical Oncotype DX scores, where it achieved an AUC of 0.839, a 5.61 % improvement over the baseline model (MambaMIL), and demonstrated robust predictive performance, particularly in identifying high-risk score ranges (accuracy: 0.714 vs 0.419). Further assessments on two public breast cancer pathology image datasets using six state-of-the-art models underscored BPMambaMIL’s generalizability on research-based ODX scores and binary tumor classification tasks. By evaluating various clinical scenarios, the proposed method not only enhances the accuracy of breast cancer recurrence risk predictions but also offers a cost-effective alternative to genomic assays, thus improving clinical outcomes.</div></div>\",\"PeriodicalId\":10624,\"journal\":{\"name\":\"Computer methods and programs in biomedicine\",\"volume\":\"272 \",\"pages\":\"Article 109039\"},\"PeriodicalIF\":4.8000,\"publicationDate\":\"2025-08-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Computer methods and programs in biomedicine\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0169260725004560\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Computer methods and programs in biomedicine","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0169260725004560","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS","Score":null,"Total":0}
BPMambaMIL: A bio-inspired prototype-guided multiple instance learning for oncotype DX risk assessment in histopathology
Breast cancer remains one of the most prevalent malignancies among women, with hormone receptor-positive (HR+)/human epidermal growth factor receptor 2-negative (HER2–) breast cancers constituting a majority, with treatment decisions often guided by genomic assays such as the 21-gene recurrence score assay, Oncotype DX. Although Oncotype DX provides critical prognostic and predictive insights, its high cost and limited accessibility create substantial barriers, especially for patients with constrained financial resources. To reduce the test cost, we aim to leverage H&E-stained whole slide images (WSIs) to predict Oncotype DX risk. Since WSIs are extremely large and contain redundant information, directly processing them is both computationally expensive and prone to errors. To address these limitations, we introduce a bio-inspired prototype-guided model (BPMambaMIL), a novel weakly supervised learning framework that integrates the Mamba mechanism with prototypical guidance to predict Oncotype DX score intervals directly from pathology images. Our model was evaluated on an in-house dataset with clinical Oncotype DX scores, where it achieved an AUC of 0.839, a 5.61 % improvement over the baseline model (MambaMIL), and demonstrated robust predictive performance, particularly in identifying high-risk score ranges (accuracy: 0.714 vs 0.419). Further assessments on two public breast cancer pathology image datasets using six state-of-the-art models underscored BPMambaMIL’s generalizability on research-based ODX scores and binary tumor classification tasks. By evaluating various clinical scenarios, the proposed method not only enhances the accuracy of breast cancer recurrence risk predictions but also offers a cost-effective alternative to genomic assays, thus improving clinical outcomes.
期刊介绍:
To encourage the development of formal computing methods, and their application in biomedical research and medical practice, by illustration of fundamental principles in biomedical informatics research; to stimulate basic research into application software design; to report the state of research of biomedical information processing projects; to report new computer methodologies applied in biomedical areas; the eventual distribution of demonstrable software to avoid duplication of effort; to provide a forum for discussion and improvement of existing software; to optimize contact between national organizations and regional user groups by promoting an international exchange of information on formal methods, standards and software in biomedicine.
Computer Methods and Programs in Biomedicine covers computing methodology and software systems derived from computing science for implementation in all aspects of biomedical research and medical practice. It is designed to serve: biochemists; biologists; geneticists; immunologists; neuroscientists; pharmacologists; toxicologists; clinicians; epidemiologists; psychiatrists; psychologists; cardiologists; chemists; (radio)physicists; computer scientists; programmers and systems analysts; biomedical, clinical, electrical and other engineers; teachers of medical informatics and users of educational software.