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

Cell Reports Medicine [2024]
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
ABSTRACT

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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