PLATINUM-BASED COMBINATION CHEMOTHERAPY IN ADVANCED NON-SMALL-CELL LUNG-CANCER - A RANDOMIZED PHASE-II TRIAL OF THE CANCER AND LEUKEMIA GROUP-B

被引:16
作者
GREEN, MR
KRAMAR, A
SCHILSKY, R
STOOPLER, M
ZIMMER, B
RICHARDS, F
SKARIN, A
ANDERSON, JR
机构
[1] FRONTIER SCI & TECHNOL RES FDN INC,AMHERST,NY
[2] UNIV CALIF SAN DIEGO,DEPT CHEM,LA JOLLA,CA 92093
[3] UNIV CALIF SAN DIEGO,CTR CANC,LA JOLLA,CA 92093
[4] HARVARD UNIV,SCH PUBL HLTH,BOSTON,MA 02115
[5] UNIV CHICAGO,CHICAGO,IL 60637
[6] COLUMBIA UNIV COLL PHYS & SURG,NEW YORK,NY 10032
[7] WAKE FOREST UNIV,BOWMAN GRAY SCH MED,WINSTON SALEM,NC 27103
[8] HARVARD UNIV,SCH MED,DANA FARBER CANC INST,BOSTON,MA 02115
来源
MEDICAL AND PEDIATRIC ONCOLOGY | 1990年 / 18卷 / 03期
关键词
cisplatin; cytarabine; vinblastine;
D O I
10.1002/mpo.2950180306
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The Cancer and Leukemia Group B (CALGB) utilized a randomized phase II trial design to evaluate two cisplatin‐based combinations, cisplatin‐cytarabine (ara‐C) and cisplatin‐vinblastine, in 151 patients with advanced non‐small cell lung cancer. Patients entered on study had not received prior chemotherapy. Platinum doses were equivalent in the two treatment programs. The total response rate (complete response, partial response, regression of evaluable disease) for the cisplatin‐vinblastine group was 22% (16/73). Failure‐free survival at six months for this group was 41%, survival at six months was 63%. The cisplatin‐ara‐C group had a total response rate of 9% (7/78) with a failure‐free survival at six months of 14% and a six‐month survival of 47%. Severe or life‐threatening toxicity was seen in 73% of cisplatin‐vinblastine cases and 59% of cisplatin‐ara‐C patients. Neither regimen is active enough to warrant designation as “standard therapy” for patients with M1 disease. Copyright © 1990 Wiley‐Liss, Inc., A Wiley Company
引用
收藏
页码:197 / 202
页数:6
相关论文
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