卡铂
肿瘤科
化疗
医学
免疫疗法
内科学
表皮生长因子受体
新辅助治疗
肺癌
埃罗替尼
癌症研究
顺铂
癌症
乳腺癌
作者
Chao Zhang,Yuxuan Sun,Dingcheng Yi,Ben‐Yuan Jiang,Li‐Xu Yan,Ze-Dao Liu,Lishan Peng,Wenjie Zhang,Hao Sun,Zhiyong Chen,Danhua Wang,Di Peng,Songan Chen,Siqi Li,Ze Zhang,Xiaoyue Tan,Jie Yang,Zhang-Yi Zhao,Wanting Zhang,Jian Su
标识
DOI:10.1016/j.xcrm.2024.101615
摘要
The clinical efficacy of neoadjuvant immunotherapy plus chemotherapy remains elusive in localized epidermal growth factor receptor (EGFR)-mutant non-small cell lung cancer (NSCLC). Here, we report interim results of a Simon's two-stage design, phase 2 trial using neoadjuvant sintilimab with carboplatin and nab-paclitaxel in resectable EGFR-mutant NSCLC. All 18 patients undergo radical surgery, with one patient experiencing surgery delay. Fourteen patients exhibit confirmed radiological response, with 44% achieving major pathological response (MPR) and no pathological complete response (pCR). Similar genomic alterations are observed before and after treatment without influencing the efficacy of subsequent EGFR-tyrosine kinase inhibitors (TKIs) in vitro. Infiltration and T cell receptor (TCR) clonal expansion of CCR8+ regulatory T (Treg)hi/CXCL13+ exhausted T (Tex)lo cells define a subtype of EGFR-mutant NSCLC highly resistant to immunotherapy, with the phenotype potentially serving as a promising signature to predict immunotherapy efficacy. Informed circulating tumor DNA (ctDNA) detection in EGFR-mutant NSCLC could help identify patients nonresponsive to neoadjuvant immunochemotherapy. These findings provide supportive data for the utilization of neoadjuvant immunochemotherapy and insight into immune resistance in EGFR-mutant NSCLC.
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