阿得贝利单抗(SHR-1316)联合化疗作为可切除 II 期至 III 期 NSCLC 患者围手术期治疗的一项开放标签、多中心、Ib 期临床试验。
Adebrelimab (SHR-1316) in Combination With Chemotherapy as Perioperative Treatment in Patients With Resectable Stage II to III NSCLCs: An Open-Label, Multicenter, Phase 1b Trial.
机构信息
Department of Thoracic Oncology I, Beijing Cancer Hospital, Beijing, People's Republic of China.
Guangdong Lung Cancer Institute, Guangdong Provincial People's Hospital & Guangdong Academy of Medical Sciences, Guangzhou, People's Republic of China.
出版信息
J Thorac Oncol. 2023 Feb;18(2):194-203. doi: 10.1016/j.jtho.2022.09.222. Epub 2022 Oct 1.
INTRODUCTION
This study evaluated adebrelimab (a programmed death-ligand 1 antibody) plus nab-paclitaxel and carboplatin as perioperative treatment for resectable NSCLC.
METHODS
Eligible patients had resectable stage II to III NSCLCs without driver gene. Patients received neoadjuvant treatment with three cycles of intravenous adebrelimab (20 mg/kg on day 1), nab-paclitaxel (100 mg/m on days 1, 8, and 15), and carboplatin (area under the curve 5 mg/mL per min on day 1), of each 21-day cycle before surgical resection, and followed by 16 cycles of adebrelimab (20 mg/kg on day 1 in 3 wk) adjuvant treatment. The primary end point was major pathologic response (MPR) per blinded independent pathologic review.
RESULTS
A total of 37 patients were enrolled and received planned neoadjuvant therapy. There were 34 patients (91.9%) who underwent surgery. As of data cutoff on January 25, 2022, 19 of the 37 patients (51.4%, 95% confidence interval [CI]: 35.9-66.6) achieved MPR per blinded independent pathologic review and 11 patients (29.7%, 95% CI: 17.5-45.8) achieved pathologic complete response. Furthermore, 26 patients (70.3%, 95% CI: 54.2-82.5) had an objective response per Response Evaluation Criteria in Solid Tumors version 1.1. The 12-month event-free survival rate was 77.8% (95% CI: 54.1-90.3). In addition, 29 patients (78.4%) had grade greater than or equal to three treatment-related adverse events (AEs) and nine (24.3%) had treatment-related serious AEs. No treatment-related deaths occurred. Grade greater than or equal to three surgery-related AEs within 30 or 90 days after surgery were both reported in five patients (14.7%).
CONCLUSIONS
Adebrelimab plus nab-paclitaxel and carboplatin as perioperative therapy led to a substantial proportion of MPR and high resectability, with manageable toxicities. On the basis of the phase 1b results, phase 3 trial was initiated.
简介
本研究评估了 adebrelimab(一种程序性死亡配体 1 抗体)联合 nab-紫杉醇和卡铂作为可切除 NSCLC 的围手术期治疗。
方法
符合条件的患者为无驱动基因的 II 期至 III 期可切除 NSCLC。患者接受新辅助治疗,每个 21 天周期接受三次静脉注射 adebrelimab(第 1 天 20mg/kg)、nab-紫杉醇(第 1、8 和 15 天 100mg/m)和卡铂(第 1 天曲线下面积 5mg/mL 每分),然后进行手术切除,随后进行 16 个周期的 adebrelimab(第 1 天 3 周内 20mg/kg)辅助治疗。主要终点是盲法独立病理评估的主要病理缓解(MPR)。
结果
共纳入 37 例患者,并接受了计划的新辅助治疗。有 34 例患者(91.9%)接受了手术。截至 2022 年 1 月 25 日数据截止时,37 例患者中有 19 例(51.4%,95%置信区间[CI]:35.9-66.6)经盲法独立病理评估达到 MPR,11 例(29.7%,95% CI:17.5-45.8)达到病理完全缓解。此外,26 例患者(70.3%,95% CI:54.2-82.5)根据实体瘤反应评估标准 1.1 达到客观缓解。12 个月无事件生存率为 77.8%(95% CI:54.1-90.3)。此外,29 例患者(78.4%)发生 3 级或以上治疗相关不良事件(AE),9 例(24.3%)发生治疗相关严重 AE。无治疗相关死亡。5 例患者(14.7%)术后 30 天或 90 天内发生 3 级或以上手术相关 AE。
结论
Adebrelimab 联合 nab-紫杉醇和卡铂作为围手术期治疗可导致相当比例的 MPR 和高可切除性,毒性可管理。基于 1b 期结果,启动了 3 期试验。