作者
Chao Zhang,Yuxuan Sun,Ding-Cheng 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,Yang-Si Li,Ri-Qiang Liao,Song Dong,Chong‐Rui Xu,Qing Zhou,Xue-Ning Yang,Yi‐Long Wu,Zemin Zhang,Wen‐Zhao Zhong
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.