Neoadjuvant SHR-1701 with or without chemotherapy in unresectable stage III non-small-cell lung cancer: A proof-of-concept, phase 2 trial

肿瘤科 化疗 医学 阶段(地层学) 内科学 癌症 新辅助治疗 肺癌 生物 古生物学 乳腺癌
作者
Qing Zhou,Yi Pan,Xue‐Ning Yang,Yanqiu Zhao,Guang Han,Qingsong Pang,Zhenfa Zhang,Qifeng Wang,Jun Yao,Hui Wang,Weihua Yang,Baogang Liu,Qixun Chen,Xianghui Du,Kaican Cai,Baosheng Li,Yunchao Huang,Xiao Li,Song Li,Wei Shi
出处
期刊:Cancer Cell [Cell Press]
卷期号:42 (7): 1258-1267.e2 被引量:20
标识
DOI:10.1016/j.ccell.2024.05.024
摘要

We conducted a proof-of-concept, phase 2 trial to assess neoadjuvant SHR-1701 with or without chemotherapy, followed by surgery or radiotherapy, and then consolidation SHR-1701 in unresectable stage III non-small-cell lung cancer (NSCLC). In the primary cohort of patients receiving neoadjuvant combination therapy (n = 97), both primary endpoints were met, with a post-induction objective response rate of 58% (95% confidence interval [CI] 47–68) and an 18-month event-free survival (EFS) rate of 56.6% (95% CI 45.2–66.5). Overall, 27 (25%) patients underwent surgery; all achieved R0 resection. Among them, 12 (44%) major pathological responses and seven (26%) pathological complete responses were recorded. The 18-month EFS rate was 74.1% (95% CI 53.2–86.7) in surgical patients and 57.3% (43.0–69.3) in radiotherapy-treated patients. Neoadjuvant SHR-1701 with chemotherapy, followed by surgery or radiotherapy, showed promising efficacy with a tolerable safety profile in unresectable stage III NSCLC. Surgical conversion was feasible in a notable proportion of patients and associated with better survival outcomes.
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