Randomized phase II trial of sequential chemotherapy in advanced non-small cell lung cancer (SWOG 9806): Carboplatin/gemcitabine followed by paclitaxel or cisplatin/vinorelbine followed by docetaxel

被引:39
作者
Edelman, MJ
Clark, JI
Chansky, K
Albain, K
Bhoopalam, N
Weiss, GR
Giguere, JK
Kelly, K
Crowley, J
Gandara, DR
机构
[1] Univ Maryland, Greenebaum Canc Ctr, Baltimore, MD 21201 USA
[2] Loyola Univ, Stritch Sch Med, Maywood, IL 60153 USA
[3] SW Oncol Grp, Ctr Stat, Seattle, WA USA
[4] Edward J Hines Vet Affairs Med Ctr, Hines, IL USA
[5] Univ Texas, Hlth Sci Ctr, San Antonio, TX 78285 USA
[6] Greenville Community Clin Oncol Program, Greenville, SC USA
[7] Univ Colorado, Denver, CO 80202 USA
[8] Univ Calif Davis, Ctr Canc, Sacramento, CA 95817 USA
关键词
D O I
10.1158/1078-0432.CCR-04-0002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Improving chemotherapeutic efficacy in non-small cell lung cancer (NSCLC) will require the development of new drugs or new strategies to better use currently available agents. Sequential administration offers an opportunity to increase drug diversity while maintaining dose intensity. On the basis of the data indicating the activity of taxanes as second-line therapy and the lack of efficacy for more than three cycles of platinum-based therapy, this randomized Phase II study tested the concept of planned sequential chemotherapy in advanced NSCLC. Experimental Design: Patients with selected stage IIIb, (pleural effusion)/stage IV NSCLC, performance status of 0-1 and normal organ function were eligible. Therapy: arm 1, carboplatin (area under the curve = 5.5 mg/ml x min day 1) and gemcitabine (1000 mg/m(2) days 1 and 8 every 21 days x 3) followed by paclitaxel (225 mg/m(2) every 21 days x 3) or arm 2, cisplatin (100 mg/m(2) day 1), vinorelbine (25 mg/m(2) days 1 and 8 every 21 d x 3) followed by docetaxel (75-100 mg/m(2) every 21 days x 3). Results: Two-hundred four patients were accrued, of whom, 178 were eligible and evaluable. Eighty percent of patients were stage IV on arm 1 and 85% on arm 2. Response rates were 21 and 28% on arms 1 and 2, respectively. Median, 1-year and 2-year survivals were 9 months, 34 and 13%, and 9 months, 36 and 8%, on arms 1 and 2, respectively. Conclusions: Sequential therapy, as used in this study, resulted in comparable efficacy to previous Southwest Oncology Group trials of two drug combinations in this population; however, it failed to meet criteria for further study.
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收藏
页码:5022 / 5026
页数:5
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