Radiomics Nomogram Based on Multiparametric MRI for Predicting the Hormone Receptor Status of HER2-Low Expression Breast Cancer.
1/5 보강
[OBJECTIVE] To develop and validate a multiparametric magnetic resonance imaging (mpMRI)-based radiomics nomogram to predict hormone receptor (HR) status in HER2-low breast cancer.
- 표본수 (n) 137
APA
Hou W, Wang Q, et al. (2026). Radiomics Nomogram Based on Multiparametric MRI for Predicting the Hormone Receptor Status of HER2-Low Expression Breast Cancer.. Journal of computer assisted tomography. https://doi.org/10.1097/RCT.0000000000001857
MLA
Hou W, et al.. "Radiomics Nomogram Based on Multiparametric MRI for Predicting the Hormone Receptor Status of HER2-Low Expression Breast Cancer.." Journal of computer assisted tomography, 2026.
PMID
41979448
Abstract
[OBJECTIVE] To develop and validate a multiparametric magnetic resonance imaging (mpMRI)-based radiomics nomogram to predict hormone receptor (HR) status in HER2-low breast cancer.
[METHODS] A total of 198 HER2-low expression breast cancer patients who underwent mpMRI in The First Affiliated Hospital of Anhui Medical University Hospital from January 2019 to January 2025 were retrospectively analyzed. 69.2% (n=137) of patients were HR-positive, and 30.8% (n=61) were HR-negative. Patients were divided into a training set (n=138) and a testing set (n=60) in a 7:3 ratio. Radiomics features were extracted from T2-weighted imaging (T2WI), diffusion-weighted imaging (DWI), and dynamic contrast-enhanced (DCE) images separately, and the radiomics score (radscore) was calculated. The clinical-radiological model (CM), single radiomics model (RM), and mpMRI RM were constructed, and a nomogram integrating radscore with clinical-radiological characteristics was developed. The predictive performance of the models was evaluated by receiver operating characteristic (ROC) curve analysis.
[RESULTS] The area under the curve (AUC) of mpMRI RM in the training set and the testing set was 0.940 and 0.897, respectively, which were superior to that of single-modality models. The nomogram incorporating radscore and clinical-radiological characteristics, including ADC value, T2SI radio, and enhancement pattern, demonstrated higher AUC in both the training set (AUC=0.957) and testing set (AUC=0.891) than other RMs in predicting HR status of HER2-low expression breast cancer.
[CONCLUSION] An mpMRI-based nomogram incorporating radscore and clinical-radiological characteristics showed good predictive efficacy for assessing the HR status of HER2-low expression breast cancer.
[METHODS] A total of 198 HER2-low expression breast cancer patients who underwent mpMRI in The First Affiliated Hospital of Anhui Medical University Hospital from January 2019 to January 2025 were retrospectively analyzed. 69.2% (n=137) of patients were HR-positive, and 30.8% (n=61) were HR-negative. Patients were divided into a training set (n=138) and a testing set (n=60) in a 7:3 ratio. Radiomics features were extracted from T2-weighted imaging (T2WI), diffusion-weighted imaging (DWI), and dynamic contrast-enhanced (DCE) images separately, and the radiomics score (radscore) was calculated. The clinical-radiological model (CM), single radiomics model (RM), and mpMRI RM were constructed, and a nomogram integrating radscore with clinical-radiological characteristics was developed. The predictive performance of the models was evaluated by receiver operating characteristic (ROC) curve analysis.
[RESULTS] The area under the curve (AUC) of mpMRI RM in the training set and the testing set was 0.940 and 0.897, respectively, which were superior to that of single-modality models. The nomogram incorporating radscore and clinical-radiological characteristics, including ADC value, T2SI radio, and enhancement pattern, demonstrated higher AUC in both the training set (AUC=0.957) and testing set (AUC=0.891) than other RMs in predicting HR status of HER2-low expression breast cancer.
[CONCLUSION] An mpMRI-based nomogram incorporating radscore and clinical-radiological characteristics showed good predictive efficacy for assessing the HR status of HER2-low expression breast cancer.
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