乳腺癌
医学
肿瘤科
转移
淋巴结
工作流程
基因签名
队列
免疫系统
放射科
内科学
转录组
病态的
前瞻性队列研究
基因表达谱
淋巴结转移
基因
计算生物学
生物信息学
腋窝淋巴结
文本挖掘
临床试验
一致性
生存分析
病理
疾病
免疫疗法
癌症研究
作者
Xiaodong Liu,Fan Li,Ye Xiang,Ruishan Liu,Chen-xi Wang,Lihua Zhuo,Hongwei Li,Hongchao Yao,Jie Zhang,Xingxiong Zhou,Pexi Hu,Lv Yue,Jin-ming Cao,Xu Feng,Yu-hong Huang,Ming Jie,Qian Wang,Chang-Cong Gu,Fei Wang,Haibo Qu
标识
DOI:10.1038/s41698-026-01593-w
摘要
Our study developed a multiomics-driven transformer model that combines mammography, MRI, transcriptomic and proteomic data to noninvasively predict axillary lymph node (ALN) metastasis in breast cancer. A total of 2105 patients from 10 institutions were included for model training and validation. The model achieved an AUC of 0.939 in the training cohort (n = 658) and 0.830-0.867 across three independent validation cohorts (n = 282, 971 and 194, respectively), outperforming conventional ultrasound examination. Grad-CAM visualizations highlighted the tumor edges and surrounding tissue, consistent with clinical and pathological findings. In a cohort of 194 patients, multiomics analyses linked the model output to gene and protein signatures involved in immune modulation, cytoskeletal remodeling, and epithelial-to-mesenchymal transition. Critically, the major enriched pathways identified through model-stratified analysis were independently replicated in a parallel non-model-driven analysis using ALN status, demonstrating that these signatures reflect tumor biology. Network analysis revealed gene clusters related to DNA replication and immune pathways, providing biological insights into the model's decisions. These findings suggest that the stacking model holds promise as a noninvasive decision-support tool that may complement, rather than replace, current clinical staging practices. However, integration into clinical workflows requires prospective validation.
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