Ultrasound‐based radiomics‐clinical nomogram for noninvasive prediction of residual cancer burden grading in breast cancer

Author:

Li Zhi‐Yong1,Wu Sheng‐Nan23,Lin Zhen‐Hu1,Jiang Mei‐Chen4,Chen Cong1,Liang Rong‐Xi1,Lin Wen‐Jin1,Xue En‐Sheng1

Affiliation:

1. Department of Ultrasound Fujian Medical University Union Hospital Fuzhou China

2. Department of Ultrasound, the First Affiliated Hospital Fujian Medical University Fuzhou China

3. Department of Ultrasound, National Regional Medical Center, Binhai Campus of the First Affiliated Hospital Fujian Medical University Fuzhou China

4. Department of Pathology Fujian Medical University Union Hospital Fuzhou China

Abstract

AbstractPurposeTo assess the predictive value of an ultrasound‐based radiomics‐clinical nomogram for grading residual cancer burden (RCB) in breast cancer patients.MethodsThis retrospective study of breast cancer patients who underwent neoadjuvant therapy (NAC) and ultrasound scanning between November 2020 and July 2023. First, a radiomics model was established based on ultrasound images. Subsequently, multivariate LR (logistic regression) analysis incorporating both radiomic scores and clinical factors was performed to construct a nomogram. Finally, Receiver operating characteristics (ROC) curve analysis and decision curve analysis (DCA) were employed to evaluate and validate the diagnostic accuracy and effectiveness of the nomogram.ResultsA total of 1122 patients were included in this study. Among them, 427 patients exhibited a favorable response to NAC chemotherapy, while 695 patients demonstrated a poor response to NAC therapy. The radiomics model achieved an AUC value of 0.84 in the training cohort and 0.83 in the validation cohort. The ultrasound‐based radiomics‐clinical nomogram achieved an AUC value of 0.90 in the training cohort and 0.91 in the validation cohort.ConclusionsUltrasound‐based radiomics‐clinical nomogram can accurately predict the effectiveness of NAC therapy by predicting RCB grading in breast cancer patients.

Publisher

Wiley

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