Evidence map›Paper›PMID 40934765›Full record

ArticleComputer methods and programs in biomedicine2025

BPMambaMIL: A bio-inspired prototype-guided multiple instance learning for oncotype DX risk assessment in histopathology.

Yongxin Guo, Ziyu Su, Onur C Koyun, Hao Lu, Robert Wesolowski, Gary Tozbikian, M Khalid Khan Niazi, Metin N Gurcan

Abstract read
In one paragraph

Article in Computer methods and programs in biomedicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Yongxin GuoCenter for Artificial Intelligence Research, Wake Forest University School of Medicine, Winston-Salem, NC, USA. Electronic address: yoguo@wakehealth.edu.
Ziyu SuDepartment of Pathology, The Ohio State University, Columbus, OH, USA.
Onur C KoyunCenter for Artificial Intelligence Research, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Hao LuCenter for Artificial Intelligence Research, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Robert WesolowskiDivision of Medical Oncology, Comprehensive Cancer Center, The Ohio State University College of Medicine, Columbus, OH, USA.
Gary TozbikianDepartment of Pathology, The Ohio State University, Columbus, OH, USA.
M Khalid Khan NiaziDepartment of Pathology, The Ohio State University, Columbus, OH, USA.
Metin N GurcanCenter for Artificial Intelligence Research, Wake Forest University School of Medicine, Winston-Salem, NC, USA.

Funding

An ensemble deep learning model for tumor bud detection and risk stratification in colorectal carcinoma.R01CA276301 · NCI · OHIO STATE UNIVERSITY · PI Wei Chen, Muhammad Khalid Khan Niazi · 2023 to 2026
$2.0M
Development of quantitative tools to predict patients with difficult intubation to minimize treatment related complicationsR21EB029493 · NIBIB · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI NIAZI, MUHAMMAD KHALID KHAN, SEGAL, SCOTT · 2021 to 2023
$620k
Efficient and cost-effective breast cancer risk stratification using whole slide histopathology imagesR21CA273665 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI GURCAN, METIN NAFI · 2023 to 2024
$394k
NCI NIH HHS R01 CA276301NCI NIH HHS R21 CA273665NIBIB NIH HHS R21 EB029493
6 · The paper itself

Abstract

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.

Indexed as

Breast NeoplasmsAlgorithmsFemaleHumansMultiple-Instance Learning AlgorithmsPrognosisRisk AssessmentBreast cancerComputational pathologyDeep learningMambaOncotype-DX

Identifiers

PMID40934765
PMCPMC13170144

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