Efficacy of gemcitabine plus platinum chemotherapy compared with other platinum containing regimens in advanced non-small-cell lung cancer: a meta-analysis of survival outcomes

被引:225
作者
Le Chevalier, T
Scagliotti, G
Natale, R
Danson, S
Rosell, R
Stahel, R
Thomas, P
Rudd, RM
Vansteenkiste, J
Thatcher, N
Manegold, C
Pujol, JL
van Zandwijk, N
Gridelli, C
van Meerbeeck, JP
Crino, L
Brown, A
Fitzgerald, P
Aristides, M
Schiller, JH
机构
[1] Inst Gustave Roussy, F-94800 Villejuif, France
[2] Univ Turin, I-10124 Turin, Italy
[3] Cedars Sinai Med Ctr, Los Angeles, CA 90048 USA
[4] Christie Hosp, Manchester, Lancs, England
[5] Inst Catala Oncol, Barcelona, Spain
[6] Universitaetsspital, Zurich, Switzerland
[7] Hop St Marguerite, Marseille, France
[8] Univ Hosp Louvain, Louvain, Belgium
[9] St Bartholomews Hosp, London, England
[10] Thoraxklin, Heidelberg, Germany
[11] Hop Arnaud Villeneuve, Montpellier, France
[12] Netherlands Canc Inst, Amsterdam, Netherlands
[13] Moscati Hosp, Avellino, Italy
[14] Univ Hosp Ghent, Ghent, Belgium
[15] Bellaria Hosp, Bologna, Italy
[16] M TAG, London, England
[17] M TAG, Sydney, NSW, Australia
[18] Univ Wisconsin, Madison, WI USA
关键词
meta-analysis; non-smaller-cell lung cancer; gemcitabine; metastasis; chemotherapy;
D O I
10.1016/j.lungcan.2004.10.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Gemcitabine-platinum combination activity has been clearly established in a number of phase 11 studies. It has also been compared against other combinations in many phase III trials. It is generally believed that all such regimens have an equivalent impact on survival. This meta-analysis aims to quantify the treatment effect of gemcitabine plus a platinum agent in the treatment of advanced NSCLC and compare the combination to other regimens used globally. Design: Data from a total of 4556 patients from 13 randomized trials investigating gemcitabine in combination with a platinum agent versus any other platinum-containing regimen were included in a meta-analysis of time-to-event outcomes. Results: A significant reduction in overall mortality in favor of gemcitabine-platinum regimens was observed, hazard ratio (HR) 0.90 (95% Cl: 0.84-0.96) with an absolute benefit at 1 year of 3.9%. Median survival was 9.0 months for the gemcitabine-platinum regimens and 8.2 months for the comparator regimens. Subgroup analysis of the first- and second-generation platinum-based comparator regimens also indicated a significant benefit for gemcitabine-platinum regimens, HR 0.84 (Cl: 0.71-0.9985). Analysis of third-generation agent plus platinum regimens showed a non-significant trend favoring gemcitabine-platinum regimens, HR 0.93 (Cl: 0.86-1.01). There was a significant decrease in the risk of disease progression in favor of gemcitabine-platinum regimens, HR 0.88 (Cl: 0.82-0.93). An absolute benefit of 4.2% at 1 year was estimated. Median progression-free survival was 5.1 months for gemcitabine-platinum regimens compared with 4.4 months for the comparator regimens. Sub-group analysis indicated a statistically significant progression-free survival benefit for patients assigned to gemcitabine-ptatinum treatment compared to first- and second-generation platinum regimens, HR 0.85 (Cl: 0.77-0.94), and third-generation agent plus platinum regimens, HR 0.89 (Cl: 0.82-0.96). (C) 2004 Published by Elsevier Ireland Ltd.
引用
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页码:69 / 80
页数:12
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