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比卡鲁胺治疗局限性或局部进展性前列腺癌患者:中位随访 9.7 年后比卡鲁胺早期前列腺癌计划的最终结果。

Antiandrogen monotherapy in patients with localized or locally advanced prostate cancer: final results from the bicalutamide Early Prostate Cancer programme at a median follow-up of 9.7 years.

机构信息

Department of Urology, Rigshospitalet, Copenhagen, Denmark.

出版信息

BJU Int. 2010 Apr;105(8):1074-81. doi: 10.1111/j.1464-410X.2010.09319.x.

Abstract

OBJECTIVE

To evaluate the efficacy and tolerability of bicalutamide 150 mg once-daily as immediate hormonal therapy in patients with prostate cancer or as adjuvant to radical prostatectomy or radiotherapy.

PATIENTS AND METHODS

In all, 8113 patients with localized (T1-2, N0/Nx) or locally advanced (T3-4, any N; or any T, N+) prostate cancer (all M0) were enrolled in three complementary, double-blind, placebo-controlled trials. Patients were randomized to receive standard care plus either oral bicalutamide 150 mg once-daily or oral placebo. Primary endpoints were progression-free survival (PFS) and overall survival (OS). Data were collated from individual trials and evaluated in a combined analysis.

RESULTS

Overall, at a median follow-up of 9.7 years, bicalutamide significantly improved PFS (hazard ratio 0.85, 95% confidence interval 0.79-0.91; P= 0.001). Compared with placebo there was no difference in OS (hazard ratio 1.01, P= 0.77). Patients who derived benefit from bicalutamide in terms of PFS were those with locally advanced disease, with OS significantly favouring bicalutamide in patients with locally advanced disease undergoing radiotherapy (P= 0.031). Patients with localized disease showed no clinically or statistically significant improvements in PFS; there was a survival trend in favour of placebo in patients with localized disease undergoing watchful waiting (P= 0.054). The overall tolerability of bicalutamide was consistent with previous analyses, with breast pain (73.7%) and gynaecomastia (68.8%) the most frequently reported adverse events in patients randomized to bicalutamide.

CONCLUSIONS

Bicalutamide 150 mg, either as monotherapy or adjuvant to standard care, improved PFS in patients with locally advanced prostate cancer, but not in patients with localized disease. A pre-planned subset analysis showed a benefit for OS in patients with locally advanced disease undergoing radiotherapy. Bicalutamide 150 mg might represent an alternative for patients with locally advanced prostate cancer considering androgen-deprivation therapy.

摘要

目的

评估比卡鲁胺 150mg 每日一次作为前列腺癌患者的即刻激素治疗或作为根治性前列腺切除术或放疗的辅助治疗的疗效和耐受性。

患者和方法

共有 8113 名局限性(T1-2,N0/Nx)或局部晚期(T3-4,任何 N;或任何 T,N+)前列腺癌(均为 M0)患者参加了三项互补的、双盲的、安慰剂对照试验。患者被随机分配接受标准治疗加口服比卡鲁胺 150mg 每日一次或口服安慰剂。主要终点是无进展生存期(PFS)和总生存期(OS)。数据来自于个体试验进行汇总,并在联合分析中进行评估。

结果

总体而言,中位随访 9.7 年后,比卡鲁胺显著改善了 PFS(风险比 0.85,95%置信区间 0.79-0.91;P=0.001)。与安慰剂相比,OS 无差异(风险比 1.01,P=0.77)。在 PFS 方面从比卡鲁胺中获益的患者是局部晚期疾病患者,而在接受放疗的局部晚期疾病患者中,OS 明显有利于比卡鲁胺(P=0.031)。局限性疾病患者的 PFS 没有明显的临床或统计学改善;在接受观察等待的局限性疾病患者中,安慰剂有生存趋势(P=0.054)。比卡鲁胺的总体耐受性与之前的分析一致,乳房疼痛(73.7%)和男性乳房发育(68.8%)是随机分配至比卡鲁胺的患者中最常报告的不良事件。

结论

比卡鲁胺 150mg 作为单一疗法或辅助标准治疗,改善了局部晚期前列腺癌患者的 PFS,但对局限性疾病患者无效。一项预先计划的亚组分析显示,接受放疗的局部晚期疾病患者的 OS 获益。对于考虑去势治疗的局部晚期前列腺癌患者,比卡鲁胺 150mg 可能是一种替代方案。

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