Comparison of Finasteride and Dutasteride on Risk of Prostate Cancer in Patients with Benign Prostatic Hyperplasia: A Pooled Analysis of 15 Real-world Databases.

IF 4 3区 医学 Q1 ANDROLOGY
Dae Yul Yang, Won-Woo Seo, Rae Woong Park, Sang Youl Rhee, Jae Myung Cha, Yoon Soo Hah, Chang Won Jeong, Kyung-Jin Kim, Hyeon-Jong Yang, Do Kyung Kim, Ji Yong Ha
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引用次数: 0

Abstract

Purpose: Finasteride and dutasteride are used to treat benign prostatic hyperplasia (BPH) and reduce the risk of developing prostate cancer. Finasteride blocks only the type 2 form of 5-alpha-reductase, whereas dutasteride blocks both type 1 and 2 forms of the enzyme. Previous studies suggest the possibility that dutasteride may be superior to finasteride in preventing prostate cancer. We directly compared the effects of finasteride and dutasteride on the risk of prostate cancer in patients with BPH using a pooled analysis of 15 real-world databases.

Materials and methods: We conducted a multicenter, cohort study of new-users of finasteride and dutasteride. We include patients who were prescribed 5 mg finasteride or dutasteride for the first time to treat BPH and had at least 180 days of prescription. We excluded patients with a history of prostate cancer or a prostate-specific antigen level ≥ 4 ng/mL before the study drug prescription. Cox regression analysis was performed to examine the hazard ratio (HR) for prostate cancer after propensity score (PS) matching.

Results: A total of 8,284 patients of new-users of finasteride and 8,670 patients of new-users of dutasteride were included across the 15 databases. In the overall population, compared to dutasteride, finasteride was associated with a lower risk of prostate cancer in both on-treatment and intent-to-treat time-at-risk periods. After 1:1 PS matching, 4,897 patients using finasteride and 4,897 patients using dutasteride were enrolled in the present study. No significant differences were observed for risk of prostate cancer between finasteride and dutasteride both on-treatment (HR=0.66, 95% confidence interval [CI]: 0.44-1.00; p=0.051) and intent-to-treat time-at-risk periods (HR=0.87, 95% CI: 0.67-1.14; p=0.310).

Conclusions: Using real-world databases, the present study demonstrated that dutasteride was not associated with a lower risk of prostate cancer than finasteride in patients with BPH.

比较非那雄胺和度他雄胺对良性前列腺增生患者罹患前列腺癌风险的影响:对 15 个真实世界数据库的汇总分析。
目的:非那雄胺和度他雄胺用于治疗良性前列腺增生症(BPH)和降低罹患前列腺癌的风险。非那雄胺只能阻断5-α-还原酶的2型,而度他雄胺则同时阻断酶的1型和2型。以往的研究表明,在预防前列腺癌方面,度他雄胺可能优于非那雄胺。我们通过对 15 个真实世界数据库进行汇总分析,直接比较了非那雄胺和度他雄胺对良性前列腺增生症患者罹患前列腺癌风险的影响:我们对非那雄胺和度他雄胺的新用户进行了一项多中心队列研究。研究对象包括首次获得 5 毫克非那雄胺或度他雄胺处方以治疗良性前列腺增生症且处方时间至少 180 天的患者。我们排除了有前列腺癌病史或研究药物处方前前列腺特异性抗原水平≥4纳克/毫升的患者。在进行倾向评分(PS)匹配后,我们对前列腺癌的危险比(HR)进行了考克斯回归分析:15个数据库共纳入了8284名非那雄胺新用户患者和8670名度他雄胺新用户患者。在总体人群中,与度他雄胺相比,非那雄胺在治疗中和意向治疗风险时间段内的前列腺癌风险都较低。经过1:1 PS配对后,本研究共纳入了4897名使用非那雄胺的患者和4897名使用度他雄胺的患者。在治疗期间(HR=0.66,95% 置信区间[CI]:0.44-1.00;P=0.051)和意向治疗风险期(HR=0.87,95% CI:0.67-1.14;P=0.310),非那雄胺和度他雄胺的前列腺癌风险均无明显差异:本研究利用真实世界数据库证明,与非那雄胺相比,度他雄胺与前列腺增生症患者罹患前列腺癌的风险无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
World Journal of Mens Health
World Journal of Mens Health Medicine-Psychiatry and Mental Health
CiteScore
7.60
自引率
2.10%
发文量
92
审稿时长
6 weeks
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