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比卡鲁胺150毫克联合局部或局部晚期前列腺癌患者的标准治疗:早期前列腺癌项目第二次分析结果,中位随访5.4年。

Bicalutamide 150 mg in addition to standard care in patients with localized or locally advanced prostate cancer: results from the second analysis of the early prostate cancer program at median followup of 5.4 years.

作者信息

Wirth Manfred P, See William A, McLeod David G, Iversen Peter, Morris Tom, Carroll Kevin

机构信息

Department of Urology, Technical University of Dresden, Dresden, Germany.

出版信息

J Urol. 2004 Nov;172(5 Pt 1):1865-70. doi: 10.1097/01.ju.0000140159.94703.80.

Abstract

PURPOSE

We evaluated the efficacy and tolerability of 150 mg bicalutamide daily given in addition to standard care, in patients with localized or locally advanced prostate cancer.

MATERIALS AND METHODS

The bicalutamide Early Prostate Cancer program consists of 3 randomized, double blind, placebo controlled trials prospectively designed for combined analysis. A total of 8,113 men with T1b-T4, M0, any N (N0 in 1 trial) prostate cancer were randomized to bicalutamide 150 mg/day (4,052) or placebo (4,061) in addition to standard care (radical prostatectomy, radiotherapy or watchful waiting). Primary end points were objective progression-free survival (PFS) and overall survival.

RESULTS

At median 5.4 years of followup (21.6% progression events) bicalutamide significantly improved PFS in the overall population. This result was driven by positive results in trials 24 and 25, with the North American trial (trial 23) showing no difference. Patients with locally advanced disease gained most benefit from bicalutamide in terms of PFS, irrespective of underlying therapy. Overall survival was similar in the bicalutamide and placebo groups, across the program and in each trial. Among watchful waiting patients survival appeared to be improved with bicalutamide in those with locally advanced disease, whereas survival appeared to be reduced with bicalutamide in those with localized disease. The most common adverse events with bicalutamide were gynecomastia and breast pain. Other adverse events occurred with a similarly low incidence in the 2 treatment groups.

CONCLUSIONS

This analysis confirms that bicalutamide provides benefit in patients with locally advanced disease. The current data suggest that early or adjuvant hormonal therapy for patients at low risk of disease progression, such as those with localized disease, is not appropriate.

摘要

目的

我们评估了在标准治疗基础上加用每日150mg比卡鲁胺治疗局限性或局部晚期前列腺癌患者的疗效和耐受性。

材料与方法

比卡鲁胺早期前列腺癌项目包括3项前瞻性设计用于联合分析的随机、双盲、安慰剂对照试验。共有8113例T1b - T4、M0、任何N(1项试验中为N0)期前列腺癌男性患者被随机分为接受每日150mg比卡鲁胺(4052例)或安慰剂(4061例)治疗,同时接受标准治疗(根治性前列腺切除术、放疗或观察等待)。主要终点为客观无进展生存期(PFS)和总生存期。

结果

在中位随访5.4年(21.6%发生进展事件)时,比卡鲁胺显著改善了总体人群的PFS。这一结果是由试验24和25的阳性结果驱动的,而北美试验(试验23)未显示出差异。无论采用何种基础治疗,局部晚期疾病患者从比卡鲁胺治疗中在PFS方面获益最大。在整个项目及每项试验中,比卡鲁胺组和安慰剂组的总生存期相似。在观察等待的患者中,局部晚期疾病患者使用比卡鲁胺似乎生存期有所改善,而局限性疾病患者使用比卡鲁胺生存期似乎有所降低。比卡鲁胺最常见的不良事件是乳腺增生和乳房疼痛。其他不良事件在两个治疗组中的发生率同样较低。

结论

该分析证实比卡鲁胺对局部晚期疾病患者有益。目前的数据表明,对于疾病进展风险低的患者,如局限性疾病患者,早期或辅助激素治疗并不合适。

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