A multicenter study of a predictive model for pathological complete response after neoadjuvant therapy in breast cancer using multimodal digital biomarkers

医学 乳腺癌 肿瘤科 新辅助治疗 内科学 病态的 多中心研究 完全响应 模式治疗法 稳健性(进化) 纳特 生物标志物 临床试验 治疗方法 癌症
作者
Yang Zixuan,He Jie,Taolang Li,Liu Changdong,Wang Yongsheng,REN Yu,Wenhe Zhao,Chiap Chiau Choo,Li Qiang,Xu Liang,Yue Jian,Liang Ting,Jin Lidan,Fang Xiaoyu,Shi Bohui,Shi Zhiqiang,Yuan Peng,Gnant Michael
出处
期刊:Chinese Journal of Cancer Research [AME Publishing Company]
卷期号:37 (6): 984-999 被引量:1
标识
DOI:10.21147/j.issn.1000-9604.2025.06.10
摘要

ObjectiveNeoadjuvant therapy (NAT) has become the standard treatment option for patients with locally advanced breast cancer. How to non-invasively screen out patients with pathological complete response (pCR) after NAT has become an urgent world-wide clinical problem. Our work aims to the assessment of neoadjuvant treatment response in breast cancer patients for higher accuracy prediction using innovative artificial intelligence system.MethodsIn this study, we retrospectively collected longitudinal (pre-NAT and post-NAT) multi-parametric magnetic resonance imaging (MRI) and clinicopathologic data of a total of 1,315 breast cancer patients (clinical stage I−III) who had undergone NAT followed by standard surgery and treated across 5 independent medical centers from January 2010 to January 2023. We used radiomics, 3D convolutional neural network technology and clinical data statistical analysis methods to extract and screen multimodal features, and then developed and validated a Clinical-Radiomics-Deep-Learning (CRDL) model to predict patients’ pCR outcomes based on multimodal fusion features.ResultsWe use the area under the receiver operating characteristic curve (AUC) in the primary cohort (PC) and 3 external validation cohorts (VC1−3) to evaluate the model performance. The results showed that the AUC in the PC composed of 2 medical centers was 0.947 [95% confidence interval (95% CI): 0.931−0.960], and the AUC values in VC1−3 were 0.857 (95% CI: 0.810−0.901), 0.883 (95% CI: 0.841−0.918) and 0.904 (95% CI: 0.860−0.941), respectively.ConclusionsThe CRDL model demonstrated high accuracy and robustness in predicting pCR to NAT using multimodal fusion data. This study provides a strong foundation for non-invasive assessment of pCR status in breast cancer patients following NAT and offers critical insights to guide clinical decision-making in post-NAT treatment planning.
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