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A meta-analysis and systematic review of randomized controlled trials with degarelix versus gonadotropin-releasing hormone agonists for advanced prostate cancer

机译:地加瑞克与促性腺激素释放激素激动剂对晚期前列腺癌的随机对照试验的荟萃分析和系统评价

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摘要

Our aim was to systematically evaluate the benefits of degarelix as antagonist versus agonists of gonadotropin-releasing hormones (GnRH) for the treatment of advanced prostate cancer (PC). This comparison was performed either in terms of biochemical or oncological or safety profiles. To this end we, carried out a systematic review and meta-analysis of the literature.We selected only studies directly and prospectively analyzing the two treatments in the same population (randomized phase III studies). We followed the Preferred Reporting Items for Systematic Reviews and meta-analyses process for reporting studies.After we eliminated studies according to the exclusion criteria, 9 publications were considered relevant to this review. These articles described 5 clinical trials that were eligible for inclusion. The follow-up duration in all trials did not exceed 364 days. This meta-analysis and review comprised a total of 1719 men, 1061 randomized to degarelix versus 658 to GnRH agonists treatment for advanced PC. Oncological results were evaluated only in 1 trial (CS21:408 cases) and they were not the primary endpoints of the study. Treatment emerging adverse events were reported in 61.4% and 58.8% of patients in the degarelix and GnRH agonists group, respectively (odds ratio, OR = 1.17; 95% confidence interval, 95% CI: 0.78-1.77, P > 0.1). Treatment related severe cardiovascular side effects were reported (trial CS21-30-35) in 1.6% and 3.6% of patients in the degarelix and GnRH agonists group, respectively (OR = 0.55, 95% CI: 0.26-1.14, P > 0.1).Our analysis evidences relevant limitations in particular for the comparative evaluation of the efficacy and the oncological results related to degarelix.
机译:我们的目标是系统评估地加瑞克作为促性腺激素释放激素(GnRH)拮抗剂与激动剂的疗效,以治疗晚期前列腺癌(PC)。该比较是根据生化或肿瘤学或安全性方面进行的。为此,我们对文献进行了系统的回顾和荟萃分析。我们仅选择直接和前瞻性分析同一人群中两种治疗方法的研究(随机III期研究)。我们按照系统评价的首选报告项目和报告研究的荟萃分析流程进行操作。根据排除标准取消研究后,有9种出版物被认为与该评价相关。这些文章描述了5个符合纳入条件的临床试验。所有试验的随访时间均不超过364天。这项荟萃分析和综述总共包括1719名男性,其中1061例随机分配给地加瑞克,而658例随机分配给GnRH激动剂用于晚期PC。仅在一项试验(CS21:408例)中评估了肿瘤学结果,它们不是研究的主要终点。在地加瑞克和GnRH激动剂组中,分别有61.4%和58.8%的患者报告了治疗出现的不良事件(几率,OR = 1.17; 95%置信区间,95%CI:0.78-1.77,P。> 0.1)。在地加瑞克和GnRH激动剂组中,分别有1.6%和3.6%的患者报告了与治疗有关的严重心血管副作用(试验CS21-30-35)(OR = 0.55,95%CI:0.26-1.14,P> 0.1)。我们的分析证明了相关局限性,特别是在与度加瑞克相关的疗效和肿瘤学结果的比较评估中。

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