非洲-加勒比地区男性转移性去势抵抗性前列腺癌(mCRPC)的总体和无进展生存期

The Prostate Pub Date : 2022-02-01 Epub Date: 2021-11-25 DOI:10.1002/pros.24270
Pierre-Gilles Vestris, Gilles Gourtaud, Cédric Senechal, Yvanne Sadreux, Virginie Roux, Pascal Blanchet, Laurent Brureau
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引用次数: 2

摘要

引言:在高加索人群中进行的几项研究表明,对于去势抵抗期(mCRPC)的转移性前列腺癌患者,使用多西他赛、阿比特龙或恩杂鲁胺是有益的。然而,没有关于非洲裔男性的有力数据。本研究的目的是估计这些治疗在mCRPC期患者的总生存期和无进展生存期。患者和方法:这是一项单中心回顾性研究,在2009年6月1日至2020年8月31日期间连续纳入211名mCRPC男性患者。主要终点为总生存期(OS)。次要终点为无进展生存期。进行Kaplan-Meier生存和Cox比例风险分析。结果:本研究纳入180例患者进行分析。无论在一线接受何种治疗,OS无差异(log-rank检验= 0.73),中位随访时间为20.7个月。接受激素治疗(阿比特龙或恩杂鲁胺)的mCRPC患者的无进展生存期优于接受多西他赛的患者(log-rank检验= 0.004),阿比特龙的风险比(HR) = 0.51(95%可信区间:0.39-0.67)。患者的特征是相似的,除了骨病变,不管在一线给予的治疗。经过单因素和多因素分析,只有世界卫生组织状态和诊断时的转移与进展显著相关。结论:我们的研究结果表明,在mCRPC期的非洲血统男性中,一线倾向于使用激素治疗(阿比特龙或恩杂鲁胺)阿比特龙。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Overall and progression-free survival of Afro-Caribbean men with metastatic castration-resistant prostate cancer (mCRPC).

Introduction: Several studies in the Caucasian population have shown the benefit of using docetaxel, abiraterone, or enzalutamide for patients with metastatic prostate cancer at the castration-resistant stage (mCRPC). However, there are no strong data for men of African ancestry. The objective of this study was to estimate the overall and progression-free survival of patients according to these treatments at the mCRPC stage.

Patients and methods: This was a monocentric retrospective study that consecutively included 211 men with mCRPC between June 1, 2009 and August 31, 2020. The primary end point was overall survival (OS). The secondary end point was progression-free survival. Kaplan-Meier survival and Cox proportional hazard analyses were performed.

Results: The present study included 180 patients for analyses. There was no difference in OS (log-rank test = 0.73), with a median follow-up of 20.7 months, regardless of the treatment administered in the first line. Men with mCRPC who received hormonotherapy (abiraterone or enzalutamide) showed better progression-free survival than those who received docetaxel (log-rank test = 0.004), with a particular interest for abiraterone hazard ratio (HR) = 0.51 (95% confidence interval: 0.39-0.67). The patient characteristics were similar, except for bone lesions, irrespective of the treatment administered in the first line. After univariate then multivariate analysis, only World Health Organization status and metastases at diagnosis were significantly associated with progression.

Conclusion: Our results suggest the use of hormonotherapy (abiraterone or enzalutamide) with a tendency for abiraterone in first line for men with African ancestry at the mCRPC stage.

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