Randomized trial comparing cisplatin with cisplatin plus vinorelbine in the treatment of advanced non-small-cell lung cancer: A Southwest Oncology Group study

被引:413
作者
Wozniak, AJ
Crowley, JJ
Balcerzak, SP
Weiss, GR
Spiridonidis, CH
Baker, LH
Albain, KS
Kelly, K
Taylor, SA
Gandara, DR
Livingston, RB
机构
[1] Wayne State Univ, Med Ctr, Detroit, MI 48202 USA
[2] Univ Michigan, Med Ctr, Ann Arbor, MI USA
[3] Univ Texas, Hlth Sci Ctr, San Antonio, TX USA
[4] Loyola Univ, Stritch Sch Med, Maywood, IL 60153 USA
[5] Univ Colorado, Denver, CO 80202 USA
[6] Univ Kansas, Med Ctr, Kansas City, KS 66103 USA
[7] Univ Calif Davis, Sacramento, CA 95817 USA
[8] SW Oncol Grp, Ctr Stat, Seattle, WA USA
[9] Univ Washington, Seattle, WA 98195 USA
[10] Ohio State Univ, Ctr Hlth, Columbus, OH 43210 USA
[11] Columbus Community Clin Oncol Program, Columbus, OH USA
关键词
D O I
10.1200/JCO.1998.16.7.2459
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Cisplatin has played a major role in the treatment of non-small-cell lung cancer (NSCLC). This randomized trial was performed by the Southwest Oncology Group (SWOG) to determine whether the combination of vinorelbine and cisplatin has any advantage with regard to response rate, survival, and rime to treatment failure over single-agent cisplatin in the treatment of patients with advanced NSCLC. Methods: Between October 1993 and April 1995, 432 patients with advanced stage NSCLC were randomised to receive arm I (cisplatin 100 mg/m(2) every 4 weeks) or arm II (cisplatin 100 mg/m2 every 4 weeks and vinorelbine 25 mg/m2 weekly). All patients were chemotherapy-naive, had performance status (PS) 0 or 1, and had adequate hematologic, renal, and hepatic function. Results: Four hundred fifteen patients were eligible and assessable. On arm I (cisplatin), there wets a 12% partial response rate. Arm II (cisplatin and vinorelbine) had a 26% response rate (2% complete responses and 24% partial responses, P =.0002). There was a statistically significant advantage with regard to progression-free survival (median, 2 v 4 months; P=.0001) and overall survival (median, 6 v 8 months; P =.0018) for the cisplatin and vinorelbine arm. One-year survival was 20% for cisplatin alone and 36% for the combination arm. There was more hematologic toxicity on arm II of the study (81% grades 3 and 4 granulocytopenia v 5% on arm I). Other toxicities, such as renal insufficiency, ototoxicity, and nausea and vomiting, and neuropathy were similar. Conclusion: The results of this study indicate that the combination of cisplatin and vinorelbine is a superior treatment when compared with single-agent cisplatin in the treatment of advanced NSCLC. Cisplatin and vinorelbine is the new standard for SWOG against which new therapies will be evaluated. (C) 1998 by American Society of Clinical Oncology.
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收藏
页码:2459 / 2465
页数:7
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