无线电技术
医学
化学免疫疗法
新辅助治疗
病态的
接收机工作特性
放射科
肺癌
肿瘤科
肿瘤异质性
个性化医疗
放射治疗
精密医学
靶向治疗
放射治疗计划
空间异质性
神经内分泌肿瘤
内科学
列线图
医学影像学
病理分期
危险分层
临床试验
肺
作者
Qin Peng,Ya Xu,Li Shen,Xiao Bao,Shuchang Zhou,Xiaodan Ye,Yajia Gu,Jing Gong
标识
DOI:10.1038/s41698-026-01388-z
摘要
The profound spatial and temporal heterogeneity of non-small cell lung cancer (NSCLC) drives unpredictable responses to neoadjuvant chemoimmunotherapy (NCI), highlighting the need for effective predictive biomarkers to optimize treatment. In this multicenter study, we evaluated the ability of habitat imaging to predict major pathological response (MPR) to NCI by capturing spatial-temporal tumor heterogeneity, using pre- and post-treatment CT scans from 394 patients with resectable non-small cell lung cancer across three institutions. A radiomics-based predictive framework integrating global texture descriptors, spatial heterogeneity features, and longitudinal imaging information was constructed to distinguish pathological responders from non-responders. Models based on global texture or spatial heterogeneity features alone achieved areas under the receiver operating characteristic curve (AUCs) ranging from 0.71 to 0.80 across validation cohorts, whereas the integrated model further improved discrimination, achieving an AUC of up to 0.85 in external validation. These findings demonstrate that habitat imaging provides a robust approach for predicting MPR and supporting patient stratification and personalized treatment planning in NSCLC.
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