Randomized study of adjuvant chemotherapy for completely resected stage I, II, or IIIA non-small-cell lung cancer

被引:446
作者
Scagliotti, GV
Fossati, R
Torri, V
Crinó, L
Giaccone, G
Silvano, G
Martelli, M
Clerici, M
Cognetti, F
Tonato, M
机构
[1] Univ Turin, Dept Clin & Biol Sci, S Luigi Hosp, Thorac Oncol Unit, I-10043 Orbassano, Torino, Italy
[2] Mario Negri Inst Pharmacol Res, Lab Clin Canc Res, I-20157 Milan, Italy
[3] Bellaria Hosp, Div Med Oncol, Bologna, Italy
[4] Free Univ Amsterdam, Med Ctr, Div Med Oncol, Amsterdam, Netherlands
[5] Moscati Hosp, Dept Radiat Oncol, Taranto, Italy
[6] S Camillo Forlanini Hosp, Div Thorac Surg, Rome, Italy
[7] S Giuseppe Hosp, Div Med Oncol, Milan, Italy
[8] Regina Elena Inst Canc Res, Div Med Oncol A, Rome, Italy
[9] Policlin Hosp, Div Med Oncol, Perugia, Italy
来源
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE | 2003年 / 95卷 / 19期
关键词
D O I
10.1093/jnci/djg059
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Surgery is the primary treatment for patients with stage 1, 11, or IIIA non-small-cell lung cancer (NSCLC). However, long-term survival of NSCLC patients after surgery alone is largely unsatisfactory, and the role of adjuvant chemotherapy in patient survival has not yet been established. Methods: Between January 1994 and January 1999, 1209 patients with stage 1, 11, or IIIA NSCLC were randomly assigned to receive mitomycin C (8 Mg/m(2) on day 1), vindesine (3 Mg/m(2) on days I and 8), and cisplatin (100 Mg/m(2) on day 1) every 3 weeks for three cycles (MVP group; n = 606) or no treatment (control group; n = 603) after complete resection. Randomization was stratified by investigational center, tumor size, lymph-node involvement, and the intention to perform radiotherapy. The primary endpoint was overall survival and secondary endpoints were progression-free survival and toxicity associated with adjuvant treatment. Survival curves were analyzed using the log-rank test. All statistical tests were two-sided. Results: After a median follow-up time of 64.5 months, there was no statistically significant difference between the two patient groups in overall survival (hazard ratio = 0.96, 95% confidence interval = 0.81 to 1.13; P =.589) or progression-free survival (hazard ratio = 0.89, 95% confidence interval = 0.76 to 1.03; P =.128). Only 69% of patients received the three planned cycles of MVP. Grades 3 and 4 neutropenia occurred in 16% and 12%, respectively, of patients in the MVP arm. Radiotherapy was completed by 65% of patients in the MVP arm and by 82% of patients in the control group. In the multivariable analysis, only disease stage and sex were associated with survival. Conclusion: This randomized trial failed to prospectively confirm a statistically significant role for adjuvant chemotherapy in completely resected NSCLC. Given the poor compliance with the MVP regimen used in this study, future studies should explore more effective treatments.
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页码:1453 / 1461
页数:9
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