Neoadjuvant sintilimab plus chemotherapy in EGFR-mutant NSCLC: Phase 2 trial interim results (NEOTIDE/CTONG2104).

Chao Zhang, Yu-Xuan Sun, Ding-Cheng Yi, Ben-Yuan Jiang, Li-Xu Yan, Ze-Dao Liu, Li-Shan Peng, Wen-Jie Zhang, Hao Sun, Zhi-Yong Chen, Dan-Hua Wang, Di Peng, Song-An Chen, Si-Qi Li, Ze Zhang, Xiao-Yue Tan, Jie Yang, Zhang-Yi Zhao, Wan-Ting Zhang, Jian Su, Yang-Si Li, Ri-Qiang Liao, Song Dong, Chong-Rui Xu,Qing Zhou,Xue-Ning Yang, Yi-Long Wu, Ze-Min Zhang,Wen-Zhao Zhong

Cell reports. Medicine(2024)

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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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