Mao Ning, Dai Yi, Zhou Heng, Lin Fan, Zheng Tiantian, Li Ziyin, Yang Ping, Zhao Feng, Li Qin, Wang Weiwei, Liang Yun, Xie Haizhu, Ma Heng, Zhang Lina, Guo Yuan, Song Xicheng, Zhang Haicheng, Lu Jie
Department of Radiology and Nuclear Medicine, Xuanwu Hospital Capital Medical University, Beijing 100053, P. R. China.
Department of Radiology, Yantai Yuhuangding Hospital, Qingdao University, Yantai, Shandong 264000, P. R. China.
Sci Adv. 2025 May 2;11(18):eadr1576. doi: 10.1126/sciadv.adr1576. Epub 2025 Apr 30.
Accurately predicting pathological complete response (pCR) before neoadjuvant chemotherapy (NAC) is crucial for patients with breast cancer. In this study, we developed a multimodal integrated fully automated pipeline system (MIFAPS) in forecasting pCR to NAC, using a multicenter and prospective dataset of 1004 patients with locally advanced breast cancer, incorporating pretreatment magnetic resonance imaging, whole slide image, and clinical risk factors. The results demonstrated that MIFAPS offered a favorable predictive performance in both the pooled external test set [area under the curve (AUC) = 0.882] and the prospective test set (AUC = 0.909). In addition, MIFAPS significantly outperformed single-modality models ( < 0.05). Furthermore, the high deep learning scores were associated with immune-related pathways and the promotion of antitumor cells in the microenvironment during biological basis exploration. Overall, our study demonstrates a promising approach for improving the prediction of pCR to NAC in patients with breast cancer through the integration of multimodal data.
准确预测新辅助化疗(NAC)前的病理完全缓解(pCR)对乳腺癌患者至关重要。在本研究中,我们开发了一种多模态集成全自动管道系统(MIFAPS)来预测NAC后的pCR,使用了1004例局部晚期乳腺癌患者的多中心前瞻性数据集,纳入了治疗前磁共振成像、全切片图像和临床风险因素。结果表明,MIFAPS在汇总外部测试集[曲线下面积(AUC)=0.882]和前瞻性测试集(AUC=0.909)中均具有良好的预测性能。此外,MIFAPS显著优于单模态模型(<0.05)。此外,在生物学基础探索过程中,高深度学习分数与免疫相关途径以及微环境中抗肿瘤细胞的促进有关。总体而言,我们的研究表明,通过整合多模态数据,有望改善乳腺癌患者NAC后pCR的预测。