Intermittent androgen suppression for prostate cancer: Rationale and clinical experience

被引:62
作者
Gleave, M [1 ]
Bruchovsky, N [1 ]
Goldenberg, SL [1 ]
Rennie, P [1 ]
机构
[1] Univ British Columbia, Vancouver Gen Hosp, Div Urol, Vancouver, BC V5Z 3J5, Canada
关键词
intermittent androgen suppression; androgen independent; androgen ablation; quality of life; prostate cancer;
D O I
10.1159/000052297
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
The rationale behind intermittent androgen suppression (IAS) is based on: (1) observations that androgen ablation is palliative, not curative, in most patients with prostate cancer, and that quality of life must be considered; (2) the assumption that immediate androgen ablation is superior to delayed therapy in improving survival; (3) the hypothesis that if tumour cells surviving androgen withdrawal are forced into a normal pathway of differentiation by androgen replacement, then apoptotic potential might be restored and progression to androgen independence delayed, Several centres have now tested the feasibility of IAS therapy in non-randomized groups of prostate cancer patients using serum of prostate-specific antigen levels as trigger points, Clinical data suggest that prostate cancer is amenable to control by IAS and offers clinicians an opportunity to improve patients' quality of life by balancing the benefits of immediate androgen ablation (delayed progression and prolonged survival) while reducing treatment-related side effects and expense. Whether time to progression and survival is affected in a beneficial or adverse way is being studied in randomized, prospective protocols.
引用
收藏
页码:37 / 41
页数:5
相关论文
共 22 条
[1]  
Adib RS, 1997, BRIT J UROL, V79, P235
[2]  
AKAKURA K, 1993, CANCER, V71, P2782, DOI 10.1002/1097-0142(19930501)71:9<2782::AID-CNCR2820710916>3.0.CO
[3]  
2-Z
[4]   Improved survival in patients with locally advanced prostate cancer treated with radiotherapy and goserelin [J].
Bolla, M ;
Gonzalez, D ;
Warde, P ;
Dubois, JB ;
Mirimanoff, RO ;
Storme, G ;
Bernier, J ;
Kuten, A ;
Sternberg, C ;
Gil, T ;
Collette, L ;
Pierart, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (05) :295-300
[5]  
BRUCHOVSKY N, 1987, PROG CLIN BIOL RES, V239, P348
[6]  
BYAR DP, 1973, CANCER, V32, P1126, DOI 10.1002/1097-0142(197311)32:5<1126::AID-CNCR2820320518>3.0.CO
[7]  
2-C
[8]  
DENIS L, 1993, CANCER, V72, P3888, DOI 10.1002/1097-0142(19931215)72:12+<3888::AID-CNCR2820721726>3.0.CO
[9]  
2-B
[10]  
Foulds L., 1969, NEOPLASTIC DEV, V1