Iversen P, Tyrrell C J, Kaisary A V, Anderson J B, Baert L, Tammela T, Chamberlain M, Carroll K, Gotting-Smith K, Blackledge G R
University of Copenhagen, Denmark.
Urology. 1998 Mar;51(3):389-96. doi: 10.1016/s0090-4295(98)00004-1.
To compare the efficacy, tolerability, and quality of life benefits of bicalutamide (Casodex) 150-mg/day monotherapy and castration in previously untreated nonmetastatic (M0) advanced prostate cancer.
A total of 480 patients with Stage T3/T4 nonmetastatic disease randomly received oral bicalutamide 150 mg/day or castration (either bilateral orchiectomy or goserelin acetate [Zoladex] 3.6 mg every 28 days) in a 2:1 ratio in two open multicenter studies (studies 306 and 307). The design of these studies was similar to allow a pooled analysis.
In the combined survival analysis, at median follow-up of 202 and 205 weeks in studies 306 and 307, respectively, with 31% of the cases resulting in death, bicalutamide 150-mg monotherapy was statistically equivalent to castration; the risk of death from any cause was 7% less with bicalutamide than with castration (hazard ratio [HR] = 0.93). Data on time to treatment failure and objective progression could not be pooled, as results for these end points differed between the trials. In study 306, bicalutamide 150-mg monotherapy increased time to objective progression (HR = 0.58; P = 0.033) and treatment failure (HR = 0.66; P = 0.074), whereas in study 307, time to progression (HR = 1.35; P = 0.0471) and treatment failure (HR = 1.24; P = 0.097) favored castration. Bicalutamide therapy showed significant advantages over castration for both sexual interest (P = 0.029) and physical capacity (P = 0.046). Bicalutamide 150-mg monotherapy was well tolerated.
Bicalutamide 150-mg monotherapy provides a similar survival outcome to castration in previously untreated patients with nonmetastatic advanced prostate cancer and confers statistically significant benefits over castration with respect to sexual interest and physical capacity.
比较比卡鲁胺(康士得)每日150毫克单药治疗与去势治疗对既往未接受过治疗的非转移性(M0)晚期前列腺癌患者的疗效、耐受性及生活质量改善情况。
在两项开放的多中心研究(研究306和307)中,共480例T3/T4期非转移性疾病患者按2:1的比例随机接受每日口服150毫克比卡鲁胺或去势治疗(双侧睾丸切除术或每28天注射3.6毫克醋酸戈舍瑞林[诺雷德])。这些研究的设计相似,以便进行汇总分析。
在联合生存分析中,研究306和307的中位随访时间分别为202周和205周,31%的病例死亡,每日150毫克比卡鲁胺单药治疗在统计学上与去势治疗等效;比卡鲁胺治疗组任何原因导致的死亡风险比去势治疗组低7%(风险比[HR]=0.93)。由于这些终点在试验中的结果不同,因此无法汇总治疗失败时间和客观进展的数据。在研究306中,每日150毫克比卡鲁胺单药治疗可延长客观进展时间(HR=0.58;P=0.033)和治疗失败时间(HR=0.66;P=0.074),而在研究307中,进展时间(HR=1.35;P=0.0471)和治疗失败时间(HR=1.24;P=0.097)则有利于去势治疗。比卡鲁胺治疗在性兴趣(P=0.029)和身体能力(P=0.046)方面均显示出优于去势治疗的显著优势。每日150毫克比卡鲁胺单药治疗耐受性良好。
对于既往未接受过治疗的非转移性晚期前列腺癌患者,每日150毫克比卡鲁胺单药治疗与去势治疗的生存结果相似,且在性兴趣和身体能力方面比去势治疗具有统计学上的显著优势。