Department of Pulmonary Medicine and Oncology, Graduate School of Medicine, Nippon Medical School, Tokyo.
Ann Oncol. 2014 Feb;25(2):529-36. doi: 10.1093/annonc/mdt552. Epub 2014 Jan 13.
This preplanned subset analysis of the phase III MONET1 study aimed to determine whether motesanib combined with carboplatin/paclitaxel (C/P) would result in improved overall survival (OS) versus chemotherapy alone, in a subset of Asian patients with nonsquamous nonsmall-cell lung cancer (NSCLC).
Patients with nonsquamous NSCLC (stage IIIB/IV or recurrent) and no prior systemic therapy for advanced disease were randomized to IV carboplatin (AUC, 6 mg/ml min) and paclitaxel (200 mg/m2) for up to six 3-week cycles, plus either oral motesanib 125 mg q.d. or placebo. Primary end point was OS; secondary end points included progression-free survival (PFS), objective response rate (ORR), and safety.
Two hundred twenty-seven Asian patients from MONET1 were included in this descriptive analysis. Median OS was 20.9 months in the motesanib plus C/P arm and 14.5 months in the placebo plus C/P arm (P=0.0223); median PFS was 7.0 and 5.3 months, respectively, (P=0.0004); and ORR was 62% and 27%, respectively, (P<0.0001). Grade≥3 adverse events were more common in the motesanib plus C/P arm versus placebo plus C/P (79% versus 61%).
In this preplanned subset analysis of Asian patients with nonsquamous NSCLC, motesanib plus C/P significantly improved OS, PFS, and ORR versus placebo plus C/P.
NCT00460317.
这项 III 期 MONET1 研究的预先计划的亚组分析旨在确定在非鳞状非小细胞肺癌(NSCLC)的亚洲患者亚组中,与单独化疗相比,莫特塞尼布联合卡铂/紫杉醇(C/P)是否会导致总生存期(OS)得到改善。
患有非鳞状 NSCLC(IIIb/IV 期或复发)且无晚期疾病系统治疗史的患者被随机分配接受 IV 卡铂(AUC,6 mg/ml min)和紫杉醇(200 mg/m2),最多进行六个 3 周周期,同时口服莫特塞尼布 125 mg q.d. 或安慰剂。主要终点是 OS;次要终点包括无进展生存期(PFS)、客观缓解率(ORR)和安全性。
MONET1 中的 227 名亚洲患者包括在本描述性分析中。莫特塞尼布加 C/P 臂的中位 OS 为 20.9 个月,安慰剂加 C/P 臂的中位 OS 为 14.5 个月(P=0.0223);中位 PFS 分别为 7.0 和 5.3 个月(P=0.0004);ORR 分别为 62%和 27%(P<0.0001)。莫特塞尼布加 C/P 臂与安慰剂加 C/P 相比,≥3 级不良事件更为常见(79%比 61%)。
在这项非鳞状 NSCLC 亚洲患者的预先计划的亚组分析中,与安慰剂加 C/P 相比,莫特塞尼布加 C/P 显著改善了 OS、PFS 和 ORR。
NCT00460317。