KEYNOTE-867: Phase 3, Randomized, Placebo-Controlled Study of Stereotactic Body Radiotherapy (SBRT) with or without Pembrolizumab in Patients with Unresected Stage I or II Non–Small-Cell Lung Cancer (NSCLC)

医学 彭布罗利珠单抗 临床终点 阶段(地层学) 肺癌 安慰剂 放射治疗 肿瘤科 内科学 外科 随机对照试验 癌症 病理 免疫疗法 生物 古生物学 替代医学
作者
Salma K. Jabbour,B. Houghton,A.G. Robinson,X. Quantin,T. Wehler,D. Kowalski,M.J. Ahn,M. Erman,G. Giaccone,H. Borghaei,J. McLean,Y. Xu,Fabíola Isabel Suano de Souza,G. Pall
出处
期刊:International Journal of Radiation Oncology Biology Physics [Elsevier]
卷期号:114 (3): e376-e377 被引量:4
标识
DOI:10.1016/j.ijrobp.2022.07.1516
摘要

Purpose/Objective(s)

Anti–PD-(L)1-directed therapy following radiotherapy or following concurrent chemoradiation is associated with significantly longer PFS and OS in patients with advanced or metastatic NSCLC, including those with locally advanced inoperable tumors. KEYNOTE-867 (NCT03924869) evaluates the efficacy and safety of SBRT with or without pembrolizumab in patients with unresected stage I or II NSCLC.

Materials/Methods

In this phase 3, randomized, placebo-controlled study, approximately 530 adult patients with previously untreated, unresected, histologically/cytologically confirmed stage I or II (T1 to limited T3, N0, M0) NSCLC are randomized 1:1 to receive thoracic SBRT to primary tumors for ≤2 wk (Table) and either pembrolizumab 200 mg or placebo every 3 wk for 17 cycles (approximately 1 year) or until disease recurrence, development of unacceptable AEs, SBRT not started for any reason, or study withdrawal. Randomization is stratified by disease stage (I vs II), ECOG PS (0 or 1 vs 2), geographic region (East Asia vs non-East Asia), and reason for not receiving surgery (medically inoperable vs refused surgery). Imaging assessment by blinded independent central review (BICR) occurs at 12 wk (≥10 wk after SBRT completion), followed by every 16 wk for 3 y, and then every 6 mo. Primary endpoints are event-free survival (EFS) by BICR and OS. Secondary endpoints include time to death or distant metastases and safety; exploratory endpoints are time to subsequent treatment, disease-specific survival, and time to recurrence/progression on subsequent line of therapy. AEs are monitored throughout the trial until 30 d after last dose (90 for serious AEs) and graded according to NCI CTCAE version 4.0. EFS and OS are analyzed by the nonparametric Kaplan-Meier method, treatment differences by stratified log-rank test, and hazard ratios by stratified Cox proportional hazard model with Efron's method of tie handling. Enrollment started on June 17, 2019, and is ongoing at 169 sites in North America, South America, Europe, Asia and Australasia.

Results

TBD

Conclusion

TBD
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