Evidence map›Paper›PMID 40251691›Full record

ArticleBreast cancer research : BCR2025

Machine learning prediction of HER2-low expression in breast cancers based on hematoxylin-eosin-stained slides.

Jun Du, Jun Shi, Dongdong Sun, Yifei Wang, Guanfeng Liu, Jingru Chen, Wei Wang, Wenchao Zhou, Yushan Zheng, Haibo Wu

Abstract read
In one paragraph

Article in Breast cancer research : BCR, 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

10 authors.

Jun Du *Department of Pathology, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, 230036, Anhui, China.
Jun Shi *School of Software, Hefei University of Technology, Hefei, 230601, China.
Dongdong Sun *School of Computer Science and Information Engineering, Hefei University of Technology, Hefei, 230601, Anhui, China.
Yifei WangSchool of Computer Science and Information Engineering, Hefei University of Technology, Hefei, 230601, Anhui, China.
Guanfeng LiuSchool of Life Sciences, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, 230027, Anhui, China.
Jingru ChenSchool of Life Sciences, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, 230027, Anhui, China.
Wei WangDepartment of Pathology, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, 230036, Anhui, China.
Wenchao ZhouIntelligent Pathology Institute, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, 230036, Anhui, China. WZAZ@ustc.edu.cn.
Yushan ZhengSchool of Engineering Medicine, Beijing Advanced Innovation Center on Biomedical Engineering, Beihang University, Beijing, 100191, China. yszheng@buaa.edu.cn.
Haibo WuDepartment of Pathology, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, 230036, Anhui, China. wuhaibo@ustc.edu.cn.

Funding

Beijing Natural Science Foundation 7242270Fundamental Research Funds for the Central Universities of China YWF-23-Q-1075Joint Fund for Medical Artificial Intelligence MAI2023C014National Natural Science Foundation of China 61906058National Natural Science Foundation of China 62171007Research Funds of Centre for Leading Medicine and Advanced Technologies of IHM 2023IHM01043Scientific Research Project of Anhui Provincial Education Department 2023AH040404undergraduate college student innovation and entrepreneurship training program S202210358114
6 · The paper itself

Abstract

backgroundTreatment with HER2-targeted therapies is recommended for HER2-positive breast cancer patients with HER2 gene amplification or protein overexpression. Interestingly, recent clinical trials of novel HER2-targeted therapies demonstrated promising efficacy in HER2-low breast cancers, raising the prospect of including a HER2-low category (immunohistochemistry, IHC) score of 1 + or 2 + with non-amplified in-situ hybridization for HER2-targeted treatments, which necessitated the accurate detection and evaluation of HER2 expression in tumors. Traditionally, HER2 protein levels are routinely assessed by IHC in clinical practice, which not only requires significant time consumption and financial investment but is also technically challenging for many basic hospitals in developing countries. Therefore, directly predicting HER2 expression by hematoxylin-eosin (HE) staining should be of significant clinical values, and machine learning may be a potent technology to achieve this goal.

methodsIn this study, we developed an artificial intelligence (AI) classification model using whole slide image of HE-stained slides to automatically assess HER2 status.

resultsA publicly available TCGA-BRCA dataset and an in-house USTC-BC dataset were applied to evaluate our AI model and the state-of-the-art method SlideGraph + in terms of accuracy (ACC), the area under the receiver operating characteristic curve (AUC), and F1 score. Overall, our AI model achieved the superior performance in HER2 scoring in both datasets with AUC of 0.795 ± 0.028 and 0.688 ± 0.008 on the USCT-BC and TCGA-BRCA datasets, respectively. In addition, we visualized the results generated from our AI model by attention heatmaps, which proved that our AI model had strong interpretability.

conclusionOur AI model is able to directly predict HER2 expression through HE images with strong interpretability, and has a better ACC particularly in HER2-low breast cancers, which provides a method for AI evaluation of HER2 status and helps to perform HER2 evaluation economically and efficiently. It has the potential to assist pathologists to improve diagnosis and assess biomarkers for companion diagnostics.

Indexed as

Biomarkers, TumorBreast NeoplasmsErb-b2 Receptor Tyrosine KinasesMachine LearningEosine Yellowish-(YS)FemaleHematoxylinHumansImmunohistochemistryROC CurveStaining and LabelingBiomarkers, TumorEosine Yellowish-(YS)ERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesHematoxylinBreast cancerHematoxylin–eosinHER2Machine learningPrediction

Identifiers

PMID40251691
PMCPMC12008878

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.