Austin Hospital, 145 Studley Road, Heidelberg, VIC, 3084, Australia.
Saitama Cancer Center, 780, Komuro, Ina, Kitaadachi District, Saitama, 362-0806, Japan.
Int J Clin Oncol. 2022 Apr;27(4):695-706. doi: 10.1007/s10147-022-02120-0. Epub 2022 Feb 19.
CheckMate 9LA, a phase 3, randomized, open-label study in first-line advanced non-small cell lung cancer (NSCLC), showed significantly improved overall survival (OS) with nivolumab plus ipilimumab combined with 2 cycles of chemotherapy versus chemotherapy alone (4 cycles). We present results for the Asian subpopulation enrolled in Japan and China.
Patients aged ≥ 18 years with treatment-naive, histologically confirmed stage IV or recurrent NSCLC, Eastern Cooperative Oncology Group performance status 0-1 and no sensitizing EGFR/ALK mutations were randomized 1:1 to nivolumab [360 mg every 3 weeks (Q3W)] plus ipilimumab (1 mg/kg Q6W) combined with chemotherapy (Q3W for 2 cycles), or chemotherapy alone (Q3W for 4 cycles). Primary endpoint was OS; secondary endpoints included progression-free survival (PFS) and objective response rate (ORR).
Twenty-eight patients received nivolumab plus ipilimumab combined with chemotherapy and 30 received chemotherapy. At a minimum follow-up of 12.7 months, median OS was not reached with nivolumab plus ipilimumab combined with chemotherapy versus 13.3 months with chemotherapy [hazard ratio (HR) 0.33; 95% confidence interval (CI) 0.14-0.80]. Median PFS was 8.4 versus 5.4 months (HR 0.47; 95% CI 0.24-0.92) and ORR was 57% versus 23%, respectively. Grade 3-4 treatment-related adverse events were observed in 57% versus 60% of patients, respectively.
Consistent with results in the all randomized population, nivolumab plus ipilimumab combined with chemotherapy improved efficacy in the Asian subpopulation versus chemotherapy alone and had a manageable safety profile, supporting its use as first-line treatment for advanced NSCLC in Asian patients.
CheckMate 9LA 是一项 3 期、随机、开放标签的研究,纳入了一线治疗的晚期非小细胞肺癌(NSCLC)患者,结果表明纳武利尤单抗联合伊匹单抗联合化疗 2 周期与单纯化疗相比,总生存期(OS)显著改善(4 周期)。现将纳入日本和中国患者的亚组数据报告如下。
这项研究共纳入了 28 例接受纳武利尤单抗联合伊匹单抗联合化疗(每 3 周 360mg,Q3W;每 6 周 1mg/kg,Q6W)和 30 例接受单纯化疗(每 3 周,Q3W)的未经治疗、组织学证实的 IV 期或复发性 NSCLC 患者,ECOG 体能状态 0-1 分,无致敏性 EGFR/ALK 突变。主要终点为 OS;次要终点包括无进展生存期(PFS)和客观缓解率(ORR)。
在随访至少 12.7 个月时,纳武利尤单抗联合伊匹单抗联合化疗组的中位 OS 尚未达到,而化疗组为 13.3 个月[风险比(HR)为 0.33;95%置信区间(CI)为 0.14-0.80]。中位 PFS 分别为 8.4 个月和 5.4 个月(HR 为 0.47;95%CI 为 0.24-0.92),ORR 分别为 57%和 23%。两组分别有 57%和 60%的患者发生了 3-4 级治疗相关不良反应。
与全人群随机分组结果一致,纳武利尤单抗联合伊匹单抗联合化疗在亚洲亚组人群中与单纯化疗相比改善了疗效,且安全性可管理,支持其在亚洲患者中作为晚期 NSCLC 的一线治疗。