Iversen P, Tyrrell C J, Kaisary A V, Anderson J B, Van Poppel H, Tammela T L, Chamberlain M, Carroll K, Melezinek I
Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
J Urol. 2000 Nov;164(5):1579-82.
Nonsteroidal antiandrogen monotherapy may be a treatment option for some patients with advanced prostate cancer. We report a survival and safety update from an analysis of 2 studies in which patients with nonmetastatic (M0) locally advanced disease were treated with either 150 mg. bicalutamide monotherapy or castration.
Data from 2 open label, multicenter studies of identical design were pooled according to protocol. Patients with stage T3/4 prostate cancer were randomized to receive 150 mg. bicalutamide daily or castration (orchiectomy or 3.6 mg. goserelin acetate every 28 days) in a 2:1 ratio.
A total of 480 patients with locally advanced prostate cancer were randomized to treatment. After a median followup of 6.3 years mortality was 56%. There was no statistically significant difference between the 2 groups in overall survival (hazard ratio 1.05, upper 1-sided 95% confidence limit 1.31, p = 0.70) or time to progression (1.20, 1.45, p = 0.11). There were statistically significant benefits in the bicalutamide monotherapy group in the 2 quality of life parameters of sexual interest (p = 0.029) and physical capacity (p = 0.046). The highest incidences of adverse events were the pharmacological side effects of hot flashes in the castration group, and breast pain and gynecomastia in the bicalutamide group. The incidences of other types of adverse events were low. Bicalutamide was well tolerated, with few drug related withdrawals from study, and no new safety issues were identified during this longer followup.
Monotherapy with 150 mg. bicalutamide is an attractive alternative to castration in patients with locally advanced prostate cancer for whom immediate hormone therapy is indicated.
非甾体类抗雄激素单药治疗可能是部分晚期前列腺癌患者的一种治疗选择。我们报告了一项生存和安全性更新情况,该更新来自对两项研究的分析,在这两项研究中,非转移性(M0)局部晚期疾病患者接受了150毫克比卡鲁胺单药治疗或去势治疗。
根据方案汇总了两项设计相同的开放标签、多中心研究的数据。T3/4期前列腺癌患者按2:1的比例随机接受每日150毫克比卡鲁胺治疗或去势治疗(睾丸切除术或每28天注射3.6毫克醋酸戈舍瑞林)。
共有480例局部晚期前列腺癌患者被随机分配接受治疗。中位随访6.3年后,死亡率为56%。两组在总生存期(风险比1.05,单侧95%置信上限1.31,p = 0.70)或疾病进展时间(1.20,1.45,p = 0.11)方面无统计学显著差异。比卡鲁胺单药治疗组在性兴趣(p = 0.029)和身体能力(p = 0.046)这两个生活质量参数方面有统计学显著益处。不良事件的最高发生率在去势组是潮热的药物副作用,在比卡鲁胺组是乳房疼痛和男性乳房发育。其他类型不良事件的发生率较低。比卡鲁胺耐受性良好,因药物相关原因退出研究的情况很少,在这次更长时间的随访中未发现新的安全问题。
对于需要立即进行激素治疗的局部晚期前列腺癌患者,150毫克比卡鲁胺单药治疗是去势治疗的一种有吸引力的替代方案。