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一项比较纳布紫杉醇与培美曲塞作为 IIIB/IV 期非小细胞肺癌患者二线化疗的 II 期开放标签临床研究。

A phase II open-label clinical study of comparing nab-paclitaxel with pemetrexed as second-line chemotherapy for patients with stage IIIB/IV non-small-cell lung cancer.

作者信息

Liu Zhefeng, Wei Zhimin, Hu Yi, Gao Feng, Hao Lu, Fang Ping, Sun Shengjie, Li Jinyu, Jiao Shunchang

机构信息

Department of Oncology, General Hospital of Chinese PLA, 28 Fuxing Road, Beijing, 100853, China.

出版信息

Med Oncol. 2015 Aug;32(8):216. doi: 10.1007/s12032-015-0660-5. Epub 2015 Jul 14.

Abstract

Current choices of second-line chemotherapy regimens for patients with advanced non-small-cell lung cancer (NSCLC) are extremely limited. We applied a new strategy of using nab-paclitaxel as single chemotherapy regimen in second-line setting for patients with unsuccessful first-line chemotherapy. The efficacy and safety were compared with patients who received standard second-line regimen pemetrexed. Patients with stage IIIB/IV NSCLC and unsuccessful first-line platinum-based chemotherapy were randomly divided into two arms. Arm I received pemetrexed 500 mg/m(2) intravenously (i.v.) on day 1 of 3-week cycle. Arm II received nab-paclitaxel 150 mg/m(2) i.v. on days 1 and 8 of 3-week cycle. The primary endpoint was overall survival (OS). One hundred and eleven patients were randomly assigned to receive pemetrexed (n = 56) and nab-paclitaxel (n = 55). Median OSs were 9.4 months (95% CI 7.1-12.5 months) for pemetrexed and 9.9 months (95% CI 8.2-11.9 months) for nab-paclitaxel. Median PFS was 4.6 months (95% CI 2.7-6.1 months) for pemetrexed and 5.1 months (95% CI 3.9-7.4 months) for nab-paclitaxel. While no CR was reported for either treatment, PRs + SDs were seen in 32/56 (57.1%) patients in pemetrexed arm and 36/55 (65.5%) patients in nab-paclitaxel arm. Grade 3 and grade 4 adverse events were comparable between two treatment arms. New second-line chemotherapy single-regimen nab-paclitaxel showed equivalent efficacy and toxicity profiles as pemetrexed in treating patients with NSCLC.

摘要

目前,晚期非小细胞肺癌(NSCLC)患者二线化疗方案的选择极为有限。我们应用了一种新策略,即对于一线化疗失败的患者,在二线治疗中使用白蛋白结合型紫杉醇作为单药化疗方案。将其疗效和安全性与接受标准二线方案培美曲塞的患者进行比较。将ⅢB/Ⅳ期NSCLC且一线铂类化疗失败的患者随机分为两组。第一组在3周周期的第1天静脉注射(i.v.)培美曲塞500mg/m²。第二组在3周周期的第1天和第8天静脉注射白蛋白结合型紫杉醇150mg/m²。主要终点为总生存期(OS)。111例患者被随机分配接受培美曲塞(n = 56)和白蛋白结合型紫杉醇(n = 55)治疗。培美曲塞组的中位OS为9.4个月(95%CI 7.1 - 12.5个月),白蛋白结合型紫杉醇组为9.9个月(95%CI 8.2 - 11.9个月)。培美曲塞组的中位无进展生存期(PFS)为4.6个月(95%CI 2.7 - 6.1个月),白蛋白结合型紫杉醇组为5.1个月(95%CI 3.9 - 7.4个月)。虽然两种治疗均未报告完全缓解(CR),但培美曲塞组32/56(57.1%)的患者和白蛋白结合型紫杉醇组36/55(65.5%)的患者出现了部分缓解(PRs)+疾病稳定(SDs)。两个治疗组之间3级和4级不良事件相当。新的二线化疗单药方案白蛋白结合型紫杉醇在治疗NSCLC患者时显示出与培美曲塞相当的疗效和毒性特征。

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