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对于晚期非小细胞肺癌,超过三个疗程的姑息性化疗并不能带来生存获益或持续的生活质量改善。

Palliative chemotherapy beyond three courses conveys no survival or consistent quality-of-life benefits in advanced non-small-cell lung cancer.

作者信息

von Plessen C, Bergman B, Andresen O, Bremnes R M, Sundstrom S, Gilleryd M, Stephens R, Vilsvik J, Aasebo U, Sorenson S

机构信息

Department of Thoracic Medicine, Haukeland University Hospital and Institute of Medicine, University of Bergen, N-5018 Bergen, Norway.

出版信息

Br J Cancer. 2006 Oct 23;95(8):966-73. doi: 10.1038/sj.bjc.6603383. Epub 2006 Oct 3.

Abstract

This randomised multicentre trial was conducted to establish the optimal duration of palliative chemotherapy in advanced non-small-cell lung cancer (NSCLC). We compared a policy of three vs six courses of new-generation platinum-based combination chemotherapy with regard to effects on quality of life (QoL) and survival. Patients with stage IIIB or IV NSCLC and WHO performance status (PS) 0-2 were randomised to receive three (C3) or six (C6) courses of carboplatin (area under the curve (AUC) 4, Chatelut's formula, equivalent to Calvert's AUC 5) on day 1 and vinorelbine 25 mg m(-2) on days 1 and 8 of a 3-week cycle. Key end points were QoL at 18 weeks, measured with EORTC Quality of Life Questionnaire (QLQ)-C30 and QLQ-LC13, and overall survival. Secondary end points were progression-free survival and need of palliative radiotherapy. Two hundred and ninety-seven patients were randomised (C3 150, C6 147). Their median age was 65 years, 30% had PS 2 and 76% stage IV disease. Seventy-eight and 54% of C3 and C6 patients, respectively, completed all scheduled chemotherapy courses. Compliance with QoL questionnaires was 88%. There were no significant group differences in global QoL, pain or fatigue up to 26 weeks. The dyspnoea palliation rate was lower in the C3 arm at 18 and 26 weeks (P<0.05), but this finding was inconsistent across different methods of analysis. Median survival in the C3 group was 28 vs 32 weeks in the C6 group (P=0.75, HR 1.04, 95% CI 0.82-1.31). One- and 2-year survival rates were 25 and 9% vs 25 and 5% in the C3 and C6 arm, respectively. Median progression-free survival was 16 and 21 weeks in the C3 and C6 groups, respectively (P=0.21, HR 0.86, 95% CI 0.68-1.08). In conclusion, palliative chemotherapy with carboplatin and vinorelbine beyond three courses conveys no survival or consistent QoL benefits in advanced NSCLC.

摘要

本随机多中心试验旨在确定晚期非小细胞肺癌(NSCLC)姑息化疗的最佳疗程。我们比较了新一代铂类联合化疗三个疗程与六个疗程的方案对生活质量(QoL)和生存的影响。ⅢB期或Ⅳ期NSCLC且世界卫生组织体能状态(PS)为0 - 2的患者被随机分配接受三个疗程(C3组)或六个疗程(C6组)的化疗,具体方案为在3周周期的第1天给予卡铂(曲线下面积(AUC)4,Chatelut公式,相当于Calvert的AUC 5),并在第1天和第8天给予长春瑞滨25 mg/m²。主要终点为18周时用欧洲癌症研究与治疗组织生活质量问卷(QLQ)-C30和QLQ-LC13测量的QoL以及总生存期。次要终点为无进展生存期和姑息性放疗需求。297例患者被随机分组(C3组150例,C6组147例)。他们的中位年龄为65岁,30%的患者PS为2,76%的患者为Ⅳ期疾病。C3组和C6组分别有78%和54%的患者完成了所有预定的化疗疗程。QoL问卷的依从率为88%。在26周内,两组在总体QoL、疼痛或疲劳方面无显著差异。在18周和26周时,C3组的呼吸困难缓解率较低(P<0.05),但这一发现通过不同分析方法得出的结果并不一致。C3组的中位生存期为28周,C6组为32周(P = 0.75,风险比1.04,95%置信区间0.82 - 1.31)。C3组和C6组的1年和2年生存率分别为25%和9%以及25%和5%。C3组和C6组的中位无进展生存期分别为16周和21周(P = 0.21,风险比0.86,95%置信区间0.68 - 1.08)。总之,对于晚期NSCLC,超过三个疗程的卡铂和长春瑞滨姑息化疗在生存或持续的QoL改善方面并无益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abfd/2360695/3f66bca16d92/95-6603383f1.jpg

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