恩杂鲁胺在去势抵抗性前列腺癌患者中的应用:回顾性、多中心、真实生活研究。

Q1 Medicine
M. Gacci, M. Marchioni, P. De Francesco, C. Natoli, F. Calabrò, T. Losanno, Cito Giammartin, S. Serni, L. Doni, C. de Nunzio, M. De Tursi, M. Valeriani, S. Giacinti, M. Álvarez-Maestro, M. Scarcia, G. Ludovico, G. Del Bene, G. Simone, M. Ferriero, G. Tuderti, P. Bove, A. Laudisi, G. Carrieri, L. Cormio, P. Verze, R. La Rocca, M. Falsaperla, V. Frantellizzi, F. Greco, M. Di Nicola, L. Schips, L. Cindolo
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引用次数: 2

摘要

背景:转移性去势抵抗性前列腺癌(mCRPC)是前列腺癌历史的最后阶段,是一种具有较高死亡率的临床相关表型。本研究的目的是评估enzalutamide在mCRPC患者“现实生活”环境中的有效性和安全性。方法收集2017年9月至2018年9月接受恩杂鲁胺治疗的所有mCRPC患者的数据。分析了人口统计学、合并症、临床参数、结果、毒性、总生存期和无进展生存期。结果共入组158例患者。平均年龄为75.8(±8.7)岁,基线中位PSA为16.5 (IQR 7.4-47.8) ng/mL。中位随访时间为7.7个月(IQR 4 ~ 14.1)。10.1%的患者报告了3-4级不良事件。43.7%的患者出现进展。总体而言,6个月和12个月的PFS率分别为69.5% (95% CI: 61.7-78.3%)和45.6% (95% CI: 36.5-57.1%);中位基线PSA >16 ng/mL (HR:2.0, 95% CI: 1.2-3.3, p=0.005)、阿片类药物的使用(HR:3.1, 95% CI 1.9-5.0, p<0.001)、既往治疗(阿比特龙、多西他赛或阿比特龙+多西他赛)与较高的癌症进展率显著相关。相反,0-1的简短疼痛问卷(HR: 0.4, 95% CI: 0.2-0.7, p<0.001)、12周50% PSA降低(HR: 0.4, 95% CI: 0.2-0.8, p=0.006)和较长的mCRPC时间(HR: 0.4, 95% CI: 0.3-0.7, p=0.002)与较低的癌症进展率相关。结论:从“现实世界”的角度来看,我们的数据显示恩杂鲁胺对mcRPC患者有效且安全。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enzalutamide in patients with castration-resistant prostate cancer: retrospective, multicenter, real life study.
BACKGROUND Metastatic castration-resistant prostate cancer (mCRPC) is the final stage of pCa history and represents a clinically relevant phenotype with an elevated burden of mortality. The aim of the present study is to evaluate the efficacy and safety of enzalutamide in a "real-life" setting in mCRPC patients. METHODS Data about all mCRPC patients treated with enzalutamide from September 2017 to September 2018 were collected. Demographics, comorbidities, clinical parameters, outcomes, toxicity, overall survival and progression free survival were analyzed. RESULTS Overall 158 patients were enrolled. Mean age was 75.8 (±8.7) years with a baseline median PSA of 16.5 (IQR 7.4-47.8) ng/mL. The median follow-up lasted 7.7 (IQR 4-14.1) months. Of all the 10.1% of patients reported grade 3-4 adverse events. 43.7% of patients experienced a progression. Overall the 6 and 12 months PFS rates were 69.5% (95% CI: 61.7-78.3%) and the 45.6% (95% CI: 36.5-57.1%); a median baseline PSA >16 ng/mL (HR:2.0, 95% CI: 1.2-3.3, p=0.005), the use of opioid (HR:3.1, 95% CI 1.9-5.0, p<0.001), a previous treatment (abiraterone, docetaxel or abiraterone + docetaxel) were significantly associated with higher rates of cancer progression. Conversely, a brief pain questionnaire of 0-1 (HR: 0.4, 95% CI: 0.2-0.7, p<0.001), a 12 weeks 50% PSA reduction (HR: 0.4, 95% CI: 0.2-0.8, p=0.006) and a longer time to mCRPC (HR: 0.4, 95% CI: 0.3-0.7, p=0.002) were related to lower cancer progression rates. CONCLUSIONS Our data shows an effective and safe profile of enzalutamide in a "realworld" perspective in patients with mcRPC.
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来源期刊
Minerva Urologica E Nefrologica
Minerva Urologica E Nefrologica UROLOGY & NEPHROLOGY-
CiteScore
5.50
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: The journal Minerva Urologica e Nefrologica publishes scientific papers on nephrology and urology. Manuscripts may be submitted in the form of Minerva opinion editorials, editorial comments, original articles, video illustrated articles, review articles and letters to the Editor.
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