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Comparison of Finasteride and Dutasteride on Risk of Prostate Cancer in Patients with Benign Prostatic Hyperplasia: A Pooled Analysis of 15 Real-world Databases.
Yang, Dae Yul; Seo, Won-Woo; Park, Rae Woong; Rhee, Sang Youl; Cha, Jae Myung; Hah, Yoon Soo; Jeong, Chang Won; Kim, Kyung-Jin; Yang, Hyeon-Jong; Kim, Do Kyung; Ha, Ji Yong.
Afiliação
  • Yang DY; Department of Urology, Kangdong Sacred Heart Hospital, Hallym University College of Medicine, Seoul, Korea.
  • Seo WW; Department of Internal Medicine, Kangdong Sacred Heart Hospital, Hallym University College of Medicine, Seoul, Korea. wonwooda@gmail.com.
  • Park RW; Department of Biomedical Informatics, Ajou University School of Medicine, Suwon, Korea.
  • Rhee SY; Department of Endocrinology and Metabolism, Kyung Hee University College of Medicine, Seoul, Korea.
  • Cha JM; Center for Digital Health, Kyung Hee University, Seoul, Korea.
  • Hah YS; Department of Internal Medicine, Kyung Hee University Hospital at Gangdong, Kyung Hee University College of Medicine, Seoul, Korea.
  • Jeong CW; Department of Urology, Daegu Catholic University School of Medicine, Daegu, Korea.
  • Kim KJ; Central Research Center of Biomedical Research Institute, Wonkwang University Hospital, Iksan, Korea.
  • Yang HJ; Department of Internal Medicine, Ewha Womans University Medical Center, Ewha Womans University School of Medicine, Seoul, Korea.
  • Kim DK; Department of Pediatrics, Soonchunhyang University Seoul Hospital, Soonchunhyang University College of Medicine, Seoul, Korea.
  • Ha JY; Department of Urology, Soonchunhyang University Seoul Hospital, Soonchunhyang University College of Medicine, Seoul, Korea.
World J Mens Health ; 2024 May 20.
Article em En | MEDLINE | ID: mdl-38772542
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 11 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.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article