化学免疫疗法
医学
肿瘤科
内科学
代谢组学
食管鳞状细胞癌
癌症研究
食管癌
癌症
临床试验
代谢物
疾病
风险评估
代谢组
细胞
随机对照试验
生物标志物
癌
作者
Zheng-Yu Qian,Yuqing Deng,M. Xi,X M Zhang,Hui Sun,Minjie Mao,Xiao-Jing Luo,Mengmeng Li,Qihua Zhang,B. Chen,Yi‐Qian Pan,Jiayi Liu,Ming-Ming He,Haojie Chen,C. Y. Yeung,Yupeng Zheng,Jun Huang,Meng Yang,Zong-Jian Li,Zhao-Lei Zeng
标识
DOI:10.1158/2159-8290.cd-25-1449
摘要
Esophageal squamous cell carcinoma (ESCC) exhibits heterogeneous responses to chemoimmunotherapy, with only a minority achieving durable benefit, necessitating dynamic precision monitoring. Through longitudinal plasma metabolomics of 541 serial samples from 252 ESCORT-1st trial patients receiving chemoimmunotherapy plus three independent cohorts of 288 samples, we established an integrated risk assessment framework spanning the entire therapeutic continuum: (1) a baseline predictor for initial responders based on metabolite signatures; (2) an on-treatment predictor in prognosticating long-term responders among initial ones based on treatment-induced metabolic shift patterns; (3) a real-time model based on dual alteration of sphingolipid and glycerophospholipid dynamically stratifying progression risk. Meanwhile, two dietary metabolites, garlic-derived S-allyl-L-cysteine and cruciferous vegetable-derived indole-3-carbinol, were confirmed to improve outcomes by promoting NK cells infiltration and reversing CD8+ T cells exhaustion. In conclusion, we provide the first metabolomic roadmap for precision chemoimmunotherapy in ESCC, unifying baseline prediction, longitudinal surveillance, and dietary modulation into clinically actionable paradigm.
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