Adjuvant Cisplatin and Vinorelbine for Completely Resected Non-small Cell Lung Cancer Subgroup Analysis of the Lung Adjuvant Cisplatin Evaluation

被引:185
|
作者
Douillard, Jean-Yves [1 ]
Tribodet, Helene [2 ]
Aubert, Delphine [3 ]
Shepherd, Frances A. [4 ]
Rosell, Rafael [5 ]
Ding, Keyue [6 ]
Veillard, Anne-Sophie [2 ]
Seymour, Lesley [6 ]
Le Chevalier, Thierry [7 ]
Spiro, Stephen [8 ]
Stephens, Richard [9 ]
Pignon, Jean Pierre [2 ]
机构
[1] Ctr Rene Gauducheau, Dept Med Oncol, F-44805 St Herblain, France
[2] Inst Gustave Roussy, Dept Biostat & Epidemiol, Paris, France
[3] Inst Rech Pierre Fabre, Dept Stat, Boulogne, France
[4] Princess Margaret Hosp, Dept Thorac Oncol, Toronto, ON M4X 1K9, Canada
[5] Hosp Badalona Germans Trias & Pujol, Med Oncol Dept Stat, Barcelona, Spain
[6] Queens Univ, Dept Biostat & Epidemiol, NCIC Clin Trials Grp, Kingston, ON, Canada
[7] Inst Gustave Roussy, Dept Med, Paris, France
[8] Middlesex Hosp, Dept Thorac Med, Middlesex, England
[9] MRC Clin Trials Unit, Canc Div, London, England
关键词
Non-small cell lung cancer; Adjuvant cisplatin-vinorelbine; Meta-analysis; TRIALIST ASSOCIATION ANITA; POSTOPERATIVE CHEMOTHERAPY; PLUS CISPLATIN; STAGE-II; METAANALYSIS; SURVIVAL;
D O I
10.1097/JTO.0b013e3181c814e7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: To evaluate the impact of adjuvant cisplatin-vinorelbine in completely resected non-small cell lung cancer and identify patients likely to benefit from this regimen in the Lung Adjuvant Cisplatin Evaluation (LACE) database. The overall LACE meta-analysis showed survival benefit with cisplatin-based adjuvant chemotherapy (5-year survival benefit of 5.4%, hazard ratio [HR] 0.89, p = 0.004). Subgroup analysis for the cisplatin-vinorelbine regimen was prespecified in the LACE statistical analysis plan. Patients randomized to cisplatin-vinorelbine or observation were the largest subgroup (41%) and the most homogeneous in terms of drug doses and eligibility. Patients and Methods: The LACE-vinorelbine cohort included trials evaluating cisplatin-vinorelbine versus observation. Overall survival was the primary end point. Other studies randomizing patients to other chemotherapy or observation (LACE-other) were also evaluated. Results: The LACE-vinorelbine cohort included 1888 patients from four studies (Adjuvant Navelbine International Trialist Association, Big Lung Trial, International Adjuvant Lung Cancer Trial, and National Cancer Institute of Canada Clinical Trials Group JBR.10). Baseline characteristics were similar to the LACE-other but had fewer patients with stage IA (2% versus 11%). Survival improvement at 5 years was 8.9% with cisplatin-vinorelbine versus observation (HR 0.80, 95% confidence interval: 0.70-0.91, p <0.001). Stage was a significant predictor for survival (test for trend, p = 0.02; benefit at 5 years: 14.7% [stage III], 11.6% [stage II], and 1.8% [stage I]). Similar benefits were seen for disease-free survival (HR 0.75 [0.67-0.85,p <0.001], stage III [HR 0.62, 0.50-0.76], stage II [HR 0.69, 0.57-0.83], and stage I [HR 0.95, 0.76-1.19]). The overall result was statistically superior to LACE-other (LACE other HR 0.95, 0.86-1.05, interaction p = 0.04). Conclusion: In subgroup analyses, adjuvant cisplatin-vinorelbine provides a superior survival benefit and can be recommended in completely resected stages II and III non-small cell lung cancer.
引用
收藏
页码:220 / 228
页数:9
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