Bicalutamide monotherapy versus flutamide plus goserelin in prostate cancer: Updated results of a multicentric trial

被引:35
作者
Boccardo, F
Barichello, M
Battaglia, M
Carmignani, G
Comeri, G
Ferraris, V
Lilliu, S
Montefiore, F
Portoghese, F
Cortellini, P
Rigatti, P
Usai, E
Rubagotti, A
机构
[1] Univ Genoa, Dept Med Oncol, I-16132 Genoa, Italy
[2] Natl Canc Res Inst Genoa, I-16132 Genoa, Italy
[3] Univ Genoa, Biostat Unit, I-16132 Genoa, Italy
[4] Gen Hosp, Dept Urol, Venice, Italy
[5] Univ Bari, Dept Urol R, Bari, Italy
[6] Univ Genoa, Dept Urol, Genoa, Italy
[7] St Anna Hosp, Dept Urol, Como, Italy
[8] Santo Spirito Hosp, Dept Urol, Casale Monferrato, Italy
[9] S Michele Hosp, Dept Urol, Cagliari, Italy
[10] Gen Hosp, Dept Urol, Novi Ligure, Italy
[11] Reg Hosp, Dept Urol, Acquaviva Delle Fonti, Italy
[12] Gen Hosp, Dept Urol, Parma, Italy
[13] Ist Sci San Raffaele, Dept Urol, Milan, Italy
[14] Univ Cagliari, Dept Urol, Cagliari, Italy
关键词
bicalutamide; antiandrogen monotherapy; prostate cancer;
D O I
10.1016/S0302-2838(02)00435-9
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
Objectives: To compare the efficacy of bicalutamide monotherapy to maximal androgen blockade in advanced prostatic cancer. Patients and Methods: Previously untreated patients with histologically proven stage C or D (American Urological Association Staging System) disease were randomly allocated to either bicalutamide (B) or goserelin plus flutamide (G + F). After disease progression, patients treated with B were assigned to castration. The primary endpoint for this trial was overall survival. Prostate cancer-specific survival and progression were included among secondary endpoints. Results: In total 108 patients received B and 112 received G + F. At a median follow-up time of 54 months (range 1-89), 151 patients progressed and 113 died. There was no significant difference in the duration of either progression-free or overall survival. Hazards of progression, death and cancer-specific death, corrected by disease stage, tumor grade and baseline PSA level, showed that patients initially assigned to B had a higher risk of progression but a comparable risk of death and cancer-specific death with the exception of patients with G3 tumors who had an increased risk of death). Conclusions: In patients with well or moderately well differentiated tumors, B monotherapy followed by castration may offer the same survival chance as maximal androgen deprivation. In those patients it thus represents a reasonable choice that can avoid the side effects of androgen deprivation for considerable periods of time. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:481 / 489
页数:9
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