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长春瑞滨联合吉西他滨与长春瑞滨联合卡铂一线治疗晚期非小细胞肺癌的随机对照 III 期临床试验。挪威肺癌研究组。

Vinorelbine and gemcitabine vs vinorelbine and carboplatin as first-line treatment of advanced NSCLC. A phase III randomised controlled trial by the Norwegian Lung Cancer Study Group.

机构信息

Department of Thoracic Medicine, Haukeland University Hospital, Jonas Lies vei 65, 5021, Bergen, Norway.

出版信息

Br J Cancer. 2012 Jul 24;107(3):442-7. doi: 10.1038/bjc.2012.284. Epub 2012 Jul 3.

DOI:10.1038/bjc.2012.284
PMID:22759880
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3405221/
Abstract

BACKGROUND

Platinum-based doublet chemotherapy is the standard first-line treatment for advanced non-small cell lung cancer (NSCLC), but earlier studies have suggested that non-platinum combinations are equally effective and better tolerated. We conducted a national, randomised study to compare a non-platinum with a platinum combination.

METHODS

Eligible patients had stage IIIB/IV NSCLC and performance status (PS) 0-2. Patients received up to three cycles of vinorelbine 60 mg m(-2) p.o.+gemcitabine 1000 mg m(-2) i.v. day 1 and 8 (VG) or vinorelbine 60 mg m(-2) p.o. day 1 and 8+carboplatin area under the curve=5 (Calvert's formula) i.v. day 1 (VC). Patients ≥75 years received 75% of the dose. Endpoints were overall survival, health-related quality of life (HRQoL), toxicity, and the use of radiotherapy.

RESULTS

We randomised 444 patients from September 2007 to April 2009. The median age was 65 years, 58% were men and 25% had PS 2. Median survival was VG: 6.3 months; VC: 7.0 months, P=0.802. Vinorelbine plus carboplatin patients had more grade III/IV nausea/vomiting (VG: 4%, VC: 12%, P=0.008) and grade IV neutropenia (VG: 7%, VC: 19%, P<0.001). Infections, HRQoL and the use of radiotherapy did not differ significantly between the treatment groups.

CONCLUSION

The two regimens yielded similar overall survival. The VG combination had only a slightly better toxicity profile.

摘要

背景

铂类双联化疗是晚期非小细胞肺癌(NSCLC)的标准一线治疗方法,但早期研究表明非铂类联合化疗同样有效且耐受性更好。我们进行了一项全国性、随机研究,比较了非铂类联合化疗与铂类联合化疗。

方法

符合条件的患者为 IIIB/IV 期 NSCLC,表现状态(PS)为 0-2。患者接受最多三个周期的长春瑞滨 60mg/m² 口服+吉西他滨 1000mg/m² 静脉输注第 1 和 8 天(VG)或长春瑞滨 60mg/m² 口服第 1 和 8 天+卡铂 AUC=5(Calvert 公式)静脉输注第 1 天(VC)。75 岁以上患者使用 75%的剂量。终点为总生存期、健康相关生活质量(HRQoL)、毒性和放疗的使用。

结果

我们于 2007 年 9 月至 2009 年 4 月随机分配了 444 名患者。中位年龄为 65 岁,58%为男性,25%的 PS 为 2。中位生存期 VG:6.3 个月;VC:7.0 个月,P=0.802。长春瑞滨加卡铂组 III/IV 级恶心/呕吐(VG:4%,VC:12%,P=0.008)和 IV 级中性粒细胞减少(VG:7%,VC:19%,P<0.001)发生率更高。两组的感染、HRQoL 和放疗的使用没有显著差异。

结论

两种方案的总生存期相似。VG 联合方案的毒性谱略好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7dcf/3405221/243c886ce3b1/bjc2012284f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7dcf/3405221/3e299a9f4f89/bjc2012284f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7dcf/3405221/243c886ce3b1/bjc2012284f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7dcf/3405221/3e299a9f4f89/bjc2012284f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7dcf/3405221/243c886ce3b1/bjc2012284f2.jpg

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