巩固性纳武单抗与观察新辅助纳武单抗加化疗和同步放化疗(CA209-7AL)后不可切除的III期非小细胞肺癌患者:一项随机临床试验

IF 52.7 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Bo Qiu,Yuanyuan Zhao,Wenzhuo He,Weijin Zeng,Hongmei Zhang,Weineng Feng,Jun Jia,Daodu Wang,Daquan Wang,Fangjie Liu,Songran Liu,Shaohan Yin,Chuanmiao Xie,Rui Zhou,Yi Hu,Qianwen Liu,Jinyu Guo,Suping Guo,Yingjia Wu,Qiaoting Luo,Jibin Li,Yunpeng Yang,Liangping Xia,Li Zhang,Hui Liu
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引用次数: 0

摘要

CA209-7AL是一项随机、多中心、2期试验,旨在评估巩固性尼武单抗(NIVO)与新辅助NIVO +化疗和同步放化疗(CCRT)治疗不可切除的III期NSCLC的疗效和安全性。患者接受2个周期的新辅助化疗-NIVO治疗(多西紫杉醇+顺铂+ NIVO)和CCRT(总剂量54-64 Gy)。ccrt后,符合条件的患者按1:1随机分配,接受巩固NIVO(每3周360 mg,持续12个月)或观察。主要终点是随机化后的无进展生存期(PFS)。2019年12月3日至2023年8月18日,纳入264例患者,其中172例随机分为NIVO巩固组(n = 86)和观察组(n = 86)。中位随访时间为22.8个月,NIVO巩固导致的PFS明显长于观察组(中位未达到vs. 12.2个月[95% CI 10.2-20.8];分层风险比0.49 [95% CI 0.30-0.79], p = 0.003)。与一项平行的现实世界研究相比,NIVO巩固也显示出更高的PFS,其中患者接受CCRT后进行巩固性免疫治疗(中位PFS: 15.7个月[95% CI 11.9-NA])。巩固组3级或4级毒性发生率为9.3%,而观察组为4.6%,肺炎(各2.3%)和近端支气管树毒性发生率相似(3.5%对2.3%)。巩固组中有1例(1.2%)患者因肺炎导致治疗相关死亡。TMB高的患者有更长的PFS与巩固(NR比15.2个月,p = 0.042)。新辅助NIVO +化疗和CCRT后的巩固NIVO对不可切除的III期NSCLC患者显示出有效性和耐受性(ClinicalTrials.gov NCT04085250)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Consolidative nivolumab versus observation in unresectable stage III non-small cell lung cancer patients following neoadjuvant nivolumab plus chemotherapy and concurrent chemoradiotherapy (CA209-7AL): a randomized clinical trial.
CA209-7AL is a randomized, multicenter, phase 2 trial evaluating the efficacy and safety of consolidative nivolumab (NIVO) versus observation following neoadjuvant NIVO plus chemotherapy and concurrent chemoradiotherapy (CCRT) for unresectable stage III NSCLC. Patients received 2 cycles of neoadjuvant chemo-NIVO therapy (docetaxel + cisplatin + NIVO) and CCRT (total dose 54-64 Gy). Post-CCRT, eligible patients were randomized 1:1 to receive consolidative NIVO (360 mg every 3 weeks for up to 12 months) or observation. The primary endpoint was progression-free survival (PFS) from randomization. Between December 3rd, 2019, and August 18th, 2023, 264 patients were enrolled, and 172 were randomized to NIVO consolidation (n = 86) or observation (n = 86). With a median follow-up of 22·8 months, NIVO consolidation resulted in significantly longer PFS than did observation (median not reached vs. 12.2 months [95% CI 10.2-20.8]; stratified hazard ratio 0·49 [95% CI 0.30-0.79], p = 0.003). NIVO consolidation also demonstrated superior PFS compared with a parallel real-world study, where patients received CCRT followed by consolidative immunotherapy (median PFS: 15.7 months [95% CI 11.9-NA]). Grade 3 or 4 toxicities occurred in 9.3% of patients in the consolidation group versus 4·6% in the observation group, with similar rates of pneumonitis (2.3% each) and proximal bronchial tree toxicity (3.5% vs. 2.3%). Treatment-related death occurred in 1 (1.2%) patient in the consolidation group because of pneumonitis. Patients with a high TMB had a longer PFS with consolidation (NR vs. 15.2 months, p = 0.042). Consolidative NIVO following neoadjuvant NIVO plus chemotherapy and CCRT demonstrated effectiveness and tolerability for patients with unresectable stage III NSCLC (ClinicalTrials.gov NCT04085250).
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来源期刊
Signal Transduction and Targeted Therapy
Signal Transduction and Targeted Therapy Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
44.50
自引率
1.50%
发文量
384
审稿时长
5 weeks
期刊介绍: Signal Transduction and Targeted Therapy is an open access journal that focuses on timely publication of cutting-edge discoveries and advancements in basic science and clinical research related to signal transduction and targeted therapy. Scope: The journal covers research on major human diseases, including, but not limited to: Cancer,Cardiovascular diseases,Autoimmune diseases,Nervous system diseases.
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