Wang Lei, Sun Mengting, Li Jinyang, Wan Linghong, Tan Yuting, Tian Shuoran, Hou Yongying, Wu Linyu, Peng Ziyi, Hu Xiao, Zhang Qihua, Huang Zening, Han Mengyi, Peng Shiyin, Pan Yuwei, Ren Yuanfeng, Zhang Mengsi, Chen Dongfeng, Liu Qin, Li Xianfeng, Qin Zhong-Yi, Xiang Junyv, Li Mengxia, Zhu Jianwu, Chen Qiyue, Luo Huiyan, Wang Shunan, Wang Tao, Li Fan, Bian Xiu-Wu, Wang Bin
Department of Gastroenterology, Chongqing Key Laboratory of Digestive Malignancies, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, P.R. China.
School of Medicine, Chongqing University, Chongqing, P.R. China.
Clin Cancer Res. 2025 Jan 6;31(1):74-86. doi: 10.1158/1078-0432.CCR-24-2436.
Neoadjuvant immunochemotherapy (NAIC) markedly induces pathologic regression in locally advanced gastric adenocarcinoma. However, specific biomarkers are still lacking to effectively identify the beneficiary patients for NAIC.
A prospective, single-arm, phase II study was conducted to treat locally advanced gastric adenocarcinoma with NAIC (NCT05515796). Correlation between clinicopathologic characteristics and neoadjuvant efficacy was investigated. Bulk RNA sequencing data from 104 samples (from 75 patients in two independent cohorts) and single-cell RNA sequencing data from 105 treatment-naïve gastric adenocarcinomas were comprehensively analyzed to decipher the association of epithelial and microenvironmental characteristics and clinical responses.
The prespecified primary endpoints were achieved: pathologic complete regression rate was 30%, major pathologic regression rate was 43%, and the regimen was well tolerated. Analysis of baseline clinical-pathologic parameters revealed the intestinal subtype of Lauren's classification as a key feature stratifying patients with increased sensitivity to NAIC. Mechanistically, an increased pool of DNA damage repair-active cancer cells and enrichment of CLEC9A+ dendritic cells in the tumor microenvironment were associated with enhanced responsiveness of the intestinal subtype gastric adenocarcinoma to NAIC. More importantly, an intestinal subtype-specific signature model was constructed by the machine learning algorithm NaiveBayes via integrating the transcriptomic features of both DNA damage repair-active cancer cells and CLEC9A+ dendritic cells, which accurately predicted the efficacy of NAIC in multiple independent gastric adenocarcinoma cohorts.
Intestinal subtype is a histologic biomarker of enhanced sensitivity of gastric adenocarcinoma to NAIC. The intestinal subtype-specific signature model is applicable to guide NAIC for patients with locally advanced gastric adenocarcinoma.
新辅助免疫化疗(NAIC)可显著诱导局部晚期胃腺癌发生病理退缩。然而,仍缺乏有效的生物标志物来识别NAIC的受益患者。
开展一项前瞻性、单臂、II期研究,采用NAIC治疗局部晚期胃腺癌(NCT05515796)。研究了临床病理特征与新辅助疗效之间的相关性。对来自104个样本(来自两个独立队列的75例患者)的批量RNA测序数据和来自105例未经治疗的胃腺癌的单细胞RNA测序数据进行了综合分析,以阐明上皮和微环境特征与临床反应之间的关联。
达到了预先设定的主要终点:病理完全缓解率为30%,主要病理缓解率为43%,且该方案耐受性良好。对基线临床病理参数的分析显示,劳伦分类的肠型是对NAIC敏感性增加的患者分层的关键特征。从机制上讲,肿瘤微环境中DNA损伤修复活性癌细胞池的增加和CLEC9A+树突状细胞的富集与肠型胃腺癌对NAIC的反应性增强有关。更重要的是,通过机器学习算法朴素贝叶斯整合DNA损伤修复活性癌细胞和CLEC9A+树突状细胞的转录组特征,构建了一个肠型特异性特征模型,该模型准确预测了NAIC在多个独立胃腺癌队列中的疗效。
肠型是胃腺癌对NAIC敏感性增强的组织学生物标志物。肠型特异性特征模型适用于指导局部晚期胃腺癌患者的NAIC治疗。