Evidence map›Paper›PMID 41383399›Full record

ArticleFrontiers in cell and developmental biology2025

Enhancing preoperative HER2 status classification of invasive breast cancers using machine learning models based on clinicopathological and MRI features: a multicenter study.

Suhong Zhao, Zhaohua Li, Yanan Wang, Fang Zhao, Peipei Chen, Guodong Pang

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In one paragraph

Article in Frontiers in cell and developmental biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing 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

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Suhong Zhao *Department of Radiology, The Second Hospital of Shandong University, Jinan, China.
Zhaohua Li *Department of Radiology, The Second Hospital of Shandong University, Jinan, China.
Yanan WangDepartment of Radiology, Linglong Yingcheng Hospital, Yantai, China.
Fang ZhaoDepartment of Radiology, Qilu Hospital of Shandong University, Jinan, China.
Peipei ChenDepartment of Radiology, The Second Hospital of Shandong University, Jinan, China.
Guodong PangDepartment of Radiology, The Second Hospital of Shandong University, Jinan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rationale and Objectives: The human epidermal growth factor receptor 2 (HER2) gene status is crucial for determining treatment efficacy. This study assessed preoperative HER2 classification in breast cancer using machine learning based on clinicopathological and MRI characteristics. Materials and Methods: This retrospective study involved 1,015 patients (1,030 lesions) across two centers. Patients were divided into training, internal validation, and external validation sets. Nomograms were developed using clinicopathological and MRI features. Predictive models were constructed using decision trees (DT), support vector machines (SVM), k-nearest neighbors (k-NN), artificial neural networks (ANN), and multivariable logistic regression (LR). Model performance was evaluated using receiver operating characteristic curves, decision curve analysis, and calibration curves. Model interpretability was achieved by developing nomograms and employing SHAP (SHapley Additive exPlanations) analysis. Results: Key variables for distinguishing HER2-positive from HER2-negative cases included regional N category, estrogen receptor, PR (progesterone receptor) status, Ki-67 status, lesion number, distribution quadrant, and accompanying signs. The SVM model achieved the highest AUC of 0.86 (95% confidence interval (CI): 0.81-0.90) in the training set, while the ANN model had an AUC of 0.77 (95% CI: 0.67-0.86) in the internal validation set. In the external validation set, the LR model achieved the highest AUC of 0.66 (95% CI: 0.56-0.76), although the overall performance was modest. For HER2-low versus HER2-zero differentiation, Ki-67 status, lesion number, distribution quadrant, mass shape, early enhancement rate, and ADC (apparent diffusion coefficient) were significant. The SVM model attained the highest AUC of 0.87 (95% CI: 0.83-0.91) in the training set, while the LR model demonstrated superior generalizability, yielding the highest AUCs in both the internal and external validation sets (internal: 0.67, 95% CI: 0.58-0.76; external: 0.74, 95% CI: 0.65-0.83). Radiologists benefited from the nomogram for improved diagnostic accuracy, especially junior radiologists. SHAP analysis revealed that PR status was paramount for HER2-positive classification, whereas mass shape and ADC values were dominant for identifying HER2-low status. Conclusion: Integrating machine learning with clinicopathological and MRI characteristics improves the accuracy of HER2 status classification in breast cancer and enhances diagnostic capabilities for radiologists in clinical practice.

Indexed as

breast cancerclinicopathological featureshumanepidermal growth factor 2machine learningmagnetic resonance imaging

Identifiers

PMID41383399
PMCPMC12689904

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