医学
生物标志物
成像生物标志物
危险分层
肿瘤科
肺癌
病态的
内科学
放射科
计算机断层摄影术
临床试验
正电子发射断层摄影术
预测模型
癌症
新辅助治疗
队列
病理
非小细胞肺癌
肺
生物信息学
作者
Ya Xu,Shuchang Zhou,Qin Peng,Xiao Bao,Xiaodan Ye,A G Er,Tong Tong,Mirabela Rusu,Ye Gu,Mailin Chen,Jing Gong
摘要
Predicting pathological complete response (pCR) to neoadjuvant immunochemotherapy in non-small cell lung cancer (NSCLC) is clinically important yet remains challenging. Here, we introduce a foundation model-derived computed tomography (CT) imaging biomarker established from a multi-center cohort of 702 patients. Specifically, we developed and validated a non-invasive baseline CT-based model for risk stratification of pathological response. To address scanner and protocol heterogeneity, we first built a 3D Vision Mamba-based CT super-resolution model trained on 2494 cases for image standardization. We then fine-tuned a lung cancer-specific CT foundation model from a pretrained 3D model (VoCo) using 6643 chest CT scans. Finally, we constructed a multi-task Swin Transformer that jointly performs risk stratification and segments tumors to generate the imaging biomarker. Across five centers, the model achieved consistently strong generalization (AUC: 0.75-0.87) for pCR prediction. Genomic analysis revealed that the biomarker was independent of tumor mutational burden but significantly associated with TP53 mutations, suggesting an association with a radiogenomic phenotype related to this alteration. Together, these results demonstrate a generalizable and biologically meaningful foundation model-based biomarker for non-invasive risk stratification of pathological response in NSCLC.
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