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良性前列腺增生患者使用 5α-还原酶抑制剂治疗后前列腺癌特异性死亡率的系统评价和荟萃分析。

Prostate cancer specific mortality after 5α-reductase inhibitors medication in benign prostatic hyperplasia patients: systematic review and meta-analysis.

机构信息

Department of Urology, Soonchunhyang University Hospital, Soonchunhyang University College of Medicine, Seoul, Korea.

Department of Preventive Medicine, Korea University College of Medicine, Seoul, Korea.

出版信息

Aging Male. 2021 Dec;24(1):80-91. doi: 10.1080/13685538.2021.1948993.

Abstract

BACKGROUND

Our study was conducted to investigate the effect of 5-ARI on the death rate from prostate cancer by means of an updated meta-analysis using related data.

METHODS

We did comprehensive literature searches using the PubMed, Embase, and Cochrane databases through July 2019. We evaluated the risk of bias in such studies using the ROBINS-I tool and analyzed deaths from cancer and deaths from all causes using HR.

RESULTS

The meta-analysis included 11 studies. The pooled overall HRs for cancer-specific deaths between 5-ARI treatment versus non-exposed groups were 0.937 (95% CI: 0.730, 1.201). In the subgroup moderator analysis, the number of patients and additional medication variables were significantly associated with deaths from all causes ( = 0.022 and  = 0.005, respectively). For detecting the publication bias or small-study effect in the included studies, we performed Begg and Mazumdar's correlation test (0.851 and 0.573) and Egger's regression coefficient test (0.035 and 0.245) and ​suggested that there was no evidence of publication bias or small-study effect in this meta-analysis.

CONCLUSIONS

Our study indicated that exposure to 5-ARI had no close association between the overall death rate or cancer-specific deaths. To confirm these results, well-designed prospective studies with large samples are required.

摘要

背景

我们的研究通过使用相关数据进行更新的荟萃分析,旨在探讨 5-ARI 对前列腺癌死亡率的影响。

方法

我们通过 2019 年 7 月之前的 PubMed、Embase 和 Cochrane 数据库进行全面的文献检索。我们使用 ROBINS-I 工具评估这些研究的偏倚风险,并使用 HR 分析癌症相关死亡和所有原因导致的死亡。

结果

荟萃分析纳入了 11 项研究。5-ARI 治疗组与未暴露组之间癌症特异性死亡的汇总总体 HR 为 0.937(95%CI:0.730,1.201)。在亚组调节分析中,患者数量和额外药物变量与所有原因导致的死亡显著相关( = 0.022 和  = 0.005)。为了检测纳入研究中的发表偏倚或小样本效应,我们进行了 Begg 和 Mazumdar 的相关性检验(0.851 和 0.573)和 Egger 的回归系数检验(0.035 和 0.245),并表明荟萃分析中没有发表偏倚或小样本效应的证据。

结论

我们的研究表明,暴露于 5-ARI 与总体死亡率或癌症特异性死亡率之间没有密切关联。为了证实这些结果,需要进行设计良好、样本量大的前瞻性研究。

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