{"title":"Postoperative CT habitat fusion model predicts prognosis in non-small cell lung cancer after neoadjuvant immunochemotherapy","authors":"Shiyang Huang,Chaokang Han,Zhenwei Shi,Xiaonan Cui,Yue Yu,Chunhao Fang,Qian Zhou,Chen Lin,Mingyue Zou,Dingpin Huang,Jinyi Jiang,Jiajie Hu,Pingping Wu,Zaiyi Liu,Dongsheng Yue,Yilong Huang,Xianglan Zhou,Hongjie Hu,Liting Shi,Lei Shi","doi":"10.1038/s41746-026-03415-6","DOIUrl":null,"url":null,"abstract":"Abstract Neoadjuvant immunochemotherapy (NAIC) has been widely adopted for non-small cell lung cancer (NSCLC); however, reliable tools for postoperative disease-free survival (DFS) risk stratification remain lacking. We developed and validated a habitat radiomics–clinicopathological fusion model, termed the Neoadjuvant Lung Joint Clustering (NeoLung-JC) model, for postoperative DFS stratification and prediction in patients with NSCLC who underwent surgery after NAIC. The model integrates dual-sequence CT-derived tumor habitat heterogeneity scores with key clinicopathological factors. The habitat heterogeneity scores were extracted from the tumor core and peripheral regions using a joint clustering approach. In a multicenter cohort of 508 patients, the NeoLung-JC model showed favorable and consistent predictive performance, achieving a concordance index of 0.750 (95% confidence interval [CI]: 0.680–0.807) in the external validation cohort. The model significantly stratified patients into high-, medium-, and low-risk DFS groups, with clearly separated Kaplan–Meier survival curves across all cohorts ( P < 0.0001). Its prognostic performance exceeded that of conventional clinicopathological indicators, including clinical TNM (cTNM) stage, post-treatment pathological TNM (ypTNM) stage, and pathological response. By integrating dual-sequence CT-derived tumor spatial heterogeneity with clinical risk characteristics, the NeoLung-JC model may provide a useful supplementary approach for individualized postoperative prognostic assessment in patients with NSCLC undergoing surgery after NAIC.","PeriodicalId":19349,"journal":{"name":"NPJ Digital Medicine","volume":"46 1","pages":""},"PeriodicalIF":18.0000,"publicationDate":"2026-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"NPJ Digital Medicine","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1038/s41746-026-03415-6","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"HEALTH CARE SCIENCES & SERVICES","Score":null,"Total":0}
引用次数: 0
Abstract
Abstract Neoadjuvant immunochemotherapy (NAIC) has been widely adopted for non-small cell lung cancer (NSCLC); however, reliable tools for postoperative disease-free survival (DFS) risk stratification remain lacking. We developed and validated a habitat radiomics–clinicopathological fusion model, termed the Neoadjuvant Lung Joint Clustering (NeoLung-JC) model, for postoperative DFS stratification and prediction in patients with NSCLC who underwent surgery after NAIC. The model integrates dual-sequence CT-derived tumor habitat heterogeneity scores with key clinicopathological factors. The habitat heterogeneity scores were extracted from the tumor core and peripheral regions using a joint clustering approach. In a multicenter cohort of 508 patients, the NeoLung-JC model showed favorable and consistent predictive performance, achieving a concordance index of 0.750 (95% confidence interval [CI]: 0.680–0.807) in the external validation cohort. The model significantly stratified patients into high-, medium-, and low-risk DFS groups, with clearly separated Kaplan–Meier survival curves across all cohorts ( P < 0.0001). Its prognostic performance exceeded that of conventional clinicopathological indicators, including clinical TNM (cTNM) stage, post-treatment pathological TNM (ypTNM) stage, and pathological response. By integrating dual-sequence CT-derived tumor spatial heterogeneity with clinical risk characteristics, the NeoLung-JC model may provide a useful supplementary approach for individualized postoperative prognostic assessment in patients with NSCLC undergoing surgery after NAIC.
期刊介绍:
npj Digital Medicine is an online open-access journal that focuses on publishing peer-reviewed research in the field of digital medicine. The journal covers various aspects of digital medicine, including the application and implementation of digital and mobile technologies in clinical settings, virtual healthcare, and the use of artificial intelligence and informatics.
The primary goal of the journal is to support innovation and the advancement of healthcare through the integration of new digital and mobile technologies. When determining if a manuscript is suitable for publication, the journal considers four important criteria: novelty, clinical relevance, scientific rigor, and digital innovation.