首页> 外文期刊>American Journal of Clinical Oncology: Cancer Clinical Trials >Randomized phase II study of carboplatin-paclitaxel or gemcitabine- vinorelbine in patients with advanced nonsmall cell lung cancer and a performance status of 2: West Japan thoracic oncology Group 0004
【24h】

Randomized phase II study of carboplatin-paclitaxel or gemcitabine- vinorelbine in patients with advanced nonsmall cell lung cancer and a performance status of 2: West Japan thoracic oncology Group 0004

机译:卡铂-紫杉醇或吉西他滨-长春瑞滨在晚期非小细胞肺癌患者中的随机II期研究:2例工作状态为西日本胸腔肿瘤组0004

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

OBJECTIVES: The aim of the present study was to evaluate the efficacy and safety of carboplatin plus paclitaxel versus gemcitabine plus vinorelbine in patients with advanced nonsmall cell lung cancer (NSCLC) and an Eastern Cooperative Oncology Group performance status (PS) of 2. METHODS: Chemotherapy-naive patients with NSCLC of stage IIIB or IV and a PS of 2 were eligible. The patients received 3-week cycles of carboplatin (area under the curve of 6) plus paclitaxel (200 mg/m) on day 1 (CP) or gemcitabine (1000 mg/m) plus vinorelbine (25 mg/m) on days 1 and 8 (GV). The primary end point was 1-year survival rate for selection of the better treatment arm for further study. RESULTS: Of the 89 patients enrolled, 84 were assessable (41 in the CP arm, 43 in the GV arm). The overall response rate, median survival time, and 1-year survival rate were 29.3%, 5.9 months, and 22.0%, respectively, for the CP arm and 20.9%, 6.0 months, and 27.9% for the GV arm. Common toxicities of grade 3 or 4 included neutropenia (67.5% for the CP arm vs. 65.1% for the GV arm), febrile neutropenia (20% vs. 14%), and infection (25.0% vs. 23.2%). The frequency of nausea of grade 3 was greater for the CP arm (17.5% vs. 2.3%), whereas that of anemia of grade 3 or 4 (30.2% vs. 12.5%) or treatment-related death (7.0% vs. 2.4%) was greater for the GV arm. CONCLUSIONS: The 1-year survival rate did not exceed 30% for either doublet chemotherapy. Furthermore, each treatment was associated with a substantial degree of toxicity.
机译:目的:本研究的目的是评估卡铂联合紫杉醇与吉西他滨联合长春瑞滨对晚期非小细胞肺癌(NSCLC)和东部合作肿瘤小组表现状态(PS)为2的患者的疗效和安全性。方法:初治为IIIB或IV期NSCLC且PS为2的未经化疗的患者是合格的。患者在第1天(CP)接受卡铂(6曲线下面积)加紫杉醇(200 mg / m)的第3周周期,或在第1天接受吉西他滨(1000 mg / m)加长春瑞滨(25 mg / m)的3周周期和8(GV)。主要终点是1年生存率,用于选择更好的治疗方案以进一步研究。结果:在入组的89例患者中,有84例可评估(CP组41例,GV组43例)。 CP组的总缓解率,中位生存时间和1年生存率分别为CP组和GV组,分别为29.3%,5.9个月和22.0%,GV组为20.9%,6.0个月和27.9%。 3级或4级的常见毒性包括中性粒细胞减少症(CP组为67.5%,GV组为65.1%),发热性中性粒细胞减少症(20%对14%)和感染(25.0%对23.2%)。 CP臂发生3级恶心的频率更高(17.5%比2.3%),而3级或4级贫血的频率(30.2%vs. 12.5%)或与治疗相关的死亡的发生率更高(7.0%vs. 2.4 %)对于GV组来说更大。结论:两种双联化疗的1年生存率均不超过30%。此外,每种治疗都与相当程度的毒性有关。

著录项

相似文献

  • 外文文献
  • 中文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号