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化疗初治的晚期非小细胞肺癌患者中,在卡铂+白蛋白紫杉醇联合治疗后给予 Nab-紫杉醇维持治疗:多中心、开放标签、单臂 II 期试验。

Nab-paclitaxel maintenance therapy following carboplatin + nab-paclitaxel combination therapy in chemotherapy naïve patients with advanced non-small cell lung cancer: multicenter, open-label, single-arm phase II trial.

机构信息

Department of Respiratory Medicine, Fukuoka University Hospital, 7-45-1 Nanakuma, Jonan-ku, Fukuoka, Fukuoka, 814-0180, Japan.

Department of Pulmonary Medicine, Kyoto Prefectural University of Medicine, 410 Kajii-cho, Hirokoji-agaru, kawaramachi-dori, Kamigyo-ku, Kyoto, Kyoto, 602-0857, Japan.

出版信息

Invest New Drugs. 2018 Oct;36(5):903-910. doi: 10.1007/s10637-018-0617-6. Epub 2018 May 30.

Abstract

Background A global multicenter study demonstrated superiority of carboplatin + nab-paclitaxel (PTX) therapy compared to carboplatin + PTX in terms of response rate (RR) and non-inferiority in terms of progression free survival (PFS) and overall survival (OS) in untreated patients with stage IIIB/IV non-small cell lung cancer; no clinical findings have so far been reported on maintenance therapies with nab-PTX. The aim of this study was to determine the efficacy and safety of maintenance therapy with nab-PTX following carboplatin + nab-PTX combination therapy. Methods Carboplatin (AUC 6) was administered on Day 1; and nab-PTX 100 mg/m on Days 1, 8, and 15, and dosing was repeated in 4 courses of 4 weeks each. In patients with clinical response was observed at the end of the 4th course, nab-PTX maintenance therapy was repeated. Results Out of 39 patients included in the efficacy analysis, 19 (48.7%) patients completed the induction therapy and 15 (38.5%) were transitioned to maintenance therapy. The median PFS in the maintenance phase was 6.5 (90%CI 1.4-11.4) months. The median OS in 15 patients was 12.6 (95%CI: 7.4-not reached). Grade ≥ 3 toxicities observed in more than 5% of patients were neutropenia (55.0%), anemia (15.0%), and febrile neutropenia (5.0%), with no increase during the maintenance phase. Conclusions Although statistically significance was not demonstrated presumably due to a limited transition rate from induction to maintenance phase, nab-PTX was suggested to be a useful treatment option following the induction therapy with nab-PTX in patients with advanced NSCLC.

摘要

背景

一项全球性多中心研究表明,与卡铂+紫杉醇(PTX)相比,卡铂+nab-PTX 在未经治疗的 IIIB/IV 期非小细胞肺癌患者中的反应率(RR)具有优势,在无进展生存期(PFS)和总生存期(OS)方面非劣效;迄今为止,尚无关于 nab-PTX 维持治疗的临床发现。本研究旨在确定卡铂+nab-PTX 联合治疗后使用 nab-PTX 维持治疗的疗效和安全性。

方法

卡铂(AUC 6)于第 1 天给药;nab-PTX 于第 1、8 和 15 天给药,剂量为 100mg/m,每 4 周重复 4 个疗程。在第 4 个疗程结束时观察到临床反应的患者中,重复使用 nab-PTX 维持治疗。

结果

在纳入疗效分析的 39 例患者中,19 例(48.7%)患者完成了诱导治疗,15 例(38.5%)患者过渡到维持治疗。维持阶段的中位 PFS 为 6.5(90%CI 1.4-11.4)个月。15 例患者的中位 OS 为 12.6(95%CI:7.4-未达到)。观察到 15 例患者中超过 5%的患者出现≥3 级毒性,包括中性粒细胞减少症(55.0%)、贫血(15.0%)和发热性中性粒细胞减少症(5.0%),但在维持阶段无增加。

结论

尽管由于从诱导到维持阶段的转化率有限,可能未显示出统计学意义,但 nab-PTX 似乎是晚期 NSCLC 患者在接受 nab-PTX 诱导治疗后的一种有用治疗选择。

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