医学
围手术期
化疗
病态的
生物标志物
内科学
肿瘤科
免疫疗法
癌症
临床研究阶段
临床终点
临床试验
外科
前瞻性队列研究
随机对照试验
阶段(地层学)
代理终结点
多中心试验
胃肠病学
化疗方案
作者
Zhiyuan Xu,Can Hu,Litao Yang,Pengfei Yu,Yanqiang Zhang,Jiahui Chen,Guoliang Zheng,Xiaodong Chen,Tao Zhang,Weiyang He,Xiangyu Meng,Panpan Yu,Yian Du,Xiaowen Liu,Youdong Liu,Yongxiang Wang,Xiaoxiao Wu,Siwei Pan,Ruolan Zhang,Shengjie Zhang
标识
DOI:10.1016/j.ccell.2026.06.015
摘要
Perioperative immunotherapy improves outcomes in locally advanced gastric or gastroesophageal junction cancer (GC/GEJC), but reliable predictive biomarkers remain elusive. In this biomarker-stratified, randomized, multicenter phase 2 Mountain-02 trail (NCT06374901), 136 patients with operable cT3-4aN + M0 GC/GEJC were enrolled and stratified by tumor-specific MHC class II (tsMHC-II) expression status and then randomized (1:1) to receive perioperative tislelizumab plus chemotherapy or chemotherapy alone. Among tsMHC-II-positive patients, adding tislelizumab to chemotherapy significantly increased the major pathological response (mPR) rate compared with chemotherapy alone (61.8% vs. 26.5%, p = 0.003), meeting the pre-specified primary endpoint. In contrast, no significant benefit was observed in the tsMHC-II-negative subgroup. Within the combination therapy arm, tsMHC-II-positive patients also achieved numerically higher mPR (61.8% vs. 23.5%, p = 0.001) and higher pathological complete response (pCR) rate (32.4% vs. 5.9%, p = 0.006) than tsMHC-II-negative patients. These findings support tsMHC-II as a promising predictive biomarker for perioperative immunotherapy and warrant further validation in larger studies.
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