Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN.
Winship Cancer Institute, Emory University.
Clin Lung Cancer. 2022 Nov;23(7):578-584. doi: 10.1016/j.cllc.2022.07.001. Epub 2022 Jul 21.
LUN17-139 evaluated the safety and efficacy of Atezolizumab (A) plus Carboplatin (C) plus Pemetrexed (Pem) plus Bevacizumab (B) (ACBPem) in treatment naïve patients with stage IV non-squamous non-small cell lung cancer (Ns-NSCLC).
In this multicenter, single-arm phase II trial, all patients received A (1200-mg, D1) + C (AUC 5, D1) + Pem (500-mg/m2, D1) + B (15-mg/kg D1) q3 week x4. If no PD (progressive disease), patients received maintenance ABPem until PD or intolerable side effects. The primary endpoint was progression-free survival (PFS). The positive PFS result was considered as PFS>6m (historical control). Secondary endpoints included objective response rate (ORR), disease control rate (DCR) defined by complete response (CR) + partial response (PR) + stable disease (SD) ≥ 2 months, overall survival (OS), and safety.
Thirty patients were enrolled from November 2018 to October 2020. The study was closed early due to 3 patient deaths, possibly related to treatment. Median age 64 (range 38-83); Men/Women 20/10; PD-L1 TPS < 1%/1-49%/ ≥ 50% (8/15/7). The median follow-up was 20.3 months ( 1-28.1). ORR 42.9% (95% CI, 24.5-62.8%), DCR 96.4% (95% CI, 81.7-99.9%). The median PFS and OS were 11.3m (5.5-14.9,P > .05) and 22.4m (22.4-NR), respectively. Four patients had G4 toxicity (anemia, febrile-neutropenia, severe neutropenia, sepsis), and 3 patients had G5 toxicity (thromboembolism, sepsis, colonic perforation).
ABCPem was associated with increased PFS compared to historical controls but this difference did not meet the statistical significance. Three on-treatment deaths and 5 thromboembolic events prompted early closure.
LUN17-139 评估了在未经治疗的 IV 期非鳞状非小细胞肺癌(Ns-NSCLC)患者中,阿特珠单抗(A)+卡铂(C)+培美曲塞(Pem)+贝伐珠单抗(B)(ACBPem)的安全性和疗效。
在这项多中心、单臂 II 期试验中,所有患者均接受 A(1200mg,D1)+C(AUC 5,D1)+Pem(500mg/m2,D1)+B(15mg/kg,D1)q3 周 x4。如果没有疾病进展(PD),患者接受 ACBPem 维持治疗,直至 PD 或出现不可耐受的副作用。主要终点是无进展生存期(PFS)。阳性 PFS 结果被认为是 PFS>6m(历史对照)。次要终点包括客观缓解率(ORR)、完全缓解(CR)+部分缓解(PR)+稳定疾病(SD)≥2 个月的疾病控制率(DCR)、总生存期(OS)和安全性。
2018 年 11 月至 2020 年 10 月期间共纳入 30 例患者。由于 3 例患者可能与治疗相关的死亡,该研究提前关闭。中位年龄 64 岁(范围 38-83);男性/女性 20/10;PD-L1 TPS<1%/1-49%/≥50%(8/15/7)。中位随访时间为 20.3 个月(1-28.1)。ORR 为 42.9%(95%CI,24.5-62.8%),DCR 为 96.4%(95%CI,81.7-99.9%)。中位 PFS 和 OS 分别为 11.3m(5.5-14.9,P>.05)和 22.4m(22.4-NR)。4 例患者发生 4 级毒性(贫血、发热性中性粒细胞减少症、严重中性粒细胞减少症、败血症),3 例患者发生 5 级毒性(血栓栓塞事件、败血症、结肠穿孔)。
与历史对照相比,ACBPem 可增加 PFS,但差异无统计学意义。3 例治疗相关死亡和 5 例血栓栓塞事件促使研究提前关闭。