Continuous-infusion 5-fluorouracil and cisplatin for advanced/recurrent transitional cell cancer of the bladder: A Southwest Oncology Group trial

被引:3
|
作者
Kish, JA
Wolf, MK
Schellhammer, PF
Hussain, MHA
Einstein, AB
Crawford, ED
机构
[1] HENRY FORD HOSP,DETROIT,MI 48202
[2] SW ONCOL GRP,CTR STAT,SEATTLE,WA
[3] EASTERN VIRGINIA MED SCH,HAUGE MED CTR,NORFOLK,VA 23501
[4] WAYNE STATE UNIV,MED CTR,DETROIT,MI 48202
[5] UNIV S FLORIDA,H LEE MOFFITT CANC CTR,TAMPA,FL 33682
[6] UNIV COLORADO,DENVER,CO 80202
关键词
5-fluorouracil; cisplatin; advanced/recurrent bladder carcinoma;
D O I
10.1097/00000421-199708000-00001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Significant toxicities result from the use of MVAC (methotrexate, vinblastine, adriamycin, cisplatin) for advanced/recurrent transitional cell carcinoma of the bladder (ARTCCB). An alternative regimen of 5-fluorouracil (5-FU) and cisplatin was evaluated by Southwest Oncology Group (SWOG). Thirty-eight patients with ARTCCB were treated with continuous infusion 5-FU 1,000 mg/m(2)/days 1-5 and cisplatin 100 mg/day 1, on a every-21-days schedule. There were two complete responses (CR) and eight partial responses (PR) among 36 eligible patients, for an overall response rate of 28% [95% confidence interval (CI) 14-45%]. Median duration of response was 6 months, and median duration of survival was 9 months. No toxic deaths occurred. Grade 4 leukopenia occurred in 5 patients. Other toxicities were mild. Only two documented infections occurred in 5 patients with neutropenia. The response rate of 28% is better than that achieved with cisplatin alone and not dissimilar to the range of response for MVAC. Toxicities were less and tolerable. This regimen will need further evaluation.
引用
收藏
页码:327 / 330
页数:4
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