Department of Respiratory Medicine, National Hospital Organization Nagoya Medical Center, Aichi, Japan.
Department of Respiratory Medicine, National Hospital Organization Nagoya Medical Center, Aichi, Japan.
Clin Lung Cancer. 2018 Sep;19(5):e711-e715. doi: 10.1016/j.cllc.2018.05.005. Epub 2018 May 19.
Treatment with carboplatin (CBDCA) with weekly paclitaxel (PTX) has shown survival benefits compared with vinorelbine or gemcitabine in elderly patients with non-small-cell carcinoma (NSCLC). Docetaxel (DOC), however, remains a standard treatment in NSCLC. The 130-nm albumin-bound formulation of PTX (nab-PTX) has shown activity in NSCLC. Treatment with CBDCA with weekly nab-PTX showed significantly higher efficacy than CBDCA with PTX in patients with squamous histology and significantly increased overall survival (OS) in patients aged 70 years and older.
This randomized, multicenter, phase III trial (UMIN000019843) was designed to compare the efficacy and safety of CBDCA with nab-PTX with DOC in patients aged 70 years and older with advanced squamous NSCLC. Elderly patients who have received no previous chemotherapy for advanced/metastatic squamous NSCLC with Eastern Cooperative Oncology Group performance status of 0 or 1 will be randomized 1:1 to DOC (60 mg/m intravenous [I.V.] on day 1) or CBDCA (area under the blood concentration time curve 6 on day 1) with nab-PTX (100 mg/m I.V. on days 1, 8, and 15) of each 21-day cycle. The primary end point is OS. Recruitment began in December 2015 and planned enrollment is 250 patients.
If OS is greater in patients treated with CBDCA with nab-PTX than with DOC, this study will provide a new standard of care for elderly patients with squamous NSCLC.
与长春瑞滨或吉西他滨相比,卡铂(CBDCA)联合每周紫杉醇(PTX)治疗老年非小细胞肺癌(NSCLC)患者显示出生存获益。然而,多西紫杉醇(DOC)仍然是 NSCLC 的标准治疗方法。PTX 的 130nm 白蛋白结合制剂(nab-PTX)在 NSCLC 中显示出活性。与 CBDCA 联合 PTX 相比,CBDCA 联合每周 nab-PTX 治疗鳞状组织学患者的疗效显著更高,并且在 70 岁及以上患者中显著增加了总生存期(OS)。
这项随机、多中心、III 期试验(UMIN000019843)旨在比较 CBDCA 联合 nab-PTX 与 DOC 在 70 岁及以上晚期鳞状 NSCLC 患者中的疗效和安全性。先前未接受过晚期/转移性鳞状 NSCLC 化疗且东部合作肿瘤学组体能状态为 0 或 1 的老年患者将按 1:1 比例随机分配至 DOC(60mg/m 静脉[I.V.],第 1 天)或 CBDCA(第 1 天的血药浓度时间曲线下面积 6)与 nab-PTX(100mg/m I.V.,第 1、8 和 15 天),每个 21 天周期。主要终点是 OS。招募于 2015 年 12 月开始,计划入组 250 例患者。
如果 CBDCA 联合 nab-PTX 治疗的患者 OS 大于 DOC 治疗的患者,这项研究将为鳞状 NSCLC 老年患者提供新的治疗标准。