ORCHIECTOMY VERSUS BUSERELIN IN COMBINATION WITH CYPROTERONE-ACETATE, FOR 2 WEEKS OR CONTINUOUSLY, IN THE TREATMENT OF METASTATIC PROSTATIC-CANCER - PRELIMINARY-RESULTS OF EORTC-TRIAL-30843

被引:20
作者
DEVOOGT, HJ
KLIJN, JGM
STUDER, U
SCHRODER, F
SYLVESTER, R
DEPAUW, M
机构
[1] FREE UNIV AMSTERDAM HOSP, DEPT UROL, AMSTERDAM, NETHERLANDS
[2] DR DANIEL DEN HOED CLIN, ROTTERDAM, NETHERLANDS
[3] ERASMUS UNIV, DEPT UROL, 3000 DR ROTTERDAM, NETHERLANDS
[4] INSELSPITAL BERN, DEPT UROL, CH-3010 BERN, SWITZERLAND
[5] EUROPEAN ORG RES TREATMENT CANC, CTR DATA, BRUSSELS, BELGIUM
关键词
D O I
10.1016/0960-0760(90)90451-P
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This prospective randomized phase III trial compares orchidetomy as standard androgen-deprivative therapy of advanced (metastatic) prostatic cancer with treatment using the LHRH agonist Buserelin(R) administered as nasal spray 3 daily doses of 400-mu-g, and combined with cyproterone acetate (CPA) 3 daily doses of 50 mg orally for 2 weeks initially to prevent flare-up of the disease, or continuously as complete androgen blockade. The trial was closed to entry in September 1989 when 367 patients were recruited. Patients were stratified for performance status (WHO) and metastatic status prior to randomization. According to patient and disease characteristics spreading of patients over the 3 arms was without statistical significant differences. Ineligibility was 5 and 4% of the patients were only partly evaluable. In March 1990 a first, preliminary analysis was performed. At that time 207 patients were off-study for progression or death and median follow-up was 1 yr. As to time-to-progression and survival there were no significant differences between the 3 arms. The meaning of this in regard to results of other trials with complete androgen blockade is discussed.
引用
收藏
页码:965 / 969
页数:5
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