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5α-reductase inhibitors and the risk of bladder cancer in a large, population-based cohort.
Dekalo, Snir; McArthur, Eric; Campbell, Jeffrey; Ordon, Michael; Power, Nicholas; Welk, Blayne.
Afiliación
  • Dekalo S; Division of Urology, Department of Surgery, Western University, London, Ontario, Canada; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Electronic address: snirdekalo@gmail.com.
  • McArthur E; Institute for Clinical Evaluative Sciences, London, Ontario, Canada.
  • Campbell J; Division of Urology, Department of Surgery, Western University, London, Ontario, Canada.
  • Ordon M; Institute for Clinical Evaluative Sciences, London, Ontario, Canada; Division of Urology, Department of Surgery, University of Toronto, Toronto, Ontario, Canada.
  • Power N; Division of Urology, Department of Surgery, Western University, London, Ontario, Canada.
  • Welk B; Division of Urology, Department of Surgery, Western University, London, Ontario, Canada; Institute for Clinical Evaluative Sciences, London, Ontario, Canada.
Urol Oncol ; 41(1): 50.e11-50.e17, 2023 01.
Article en En | MEDLINE | ID: mdl-36319553
ABSTRACT

PURPOSE:

The ability of 5α-reductase inhibitors (5ARI) to reduce the risk of new onset bladder cancer (BC) has been studied with variable results. Our objective was to conduct a retrospective cohort population-based study to evaluate the association between 5ARI use, BC diagnosis, and BC mortality. PATIENTS AND

METHODS:

We used routinely collected health care data from Ontario, Canada. Men ≥66 years of age with a prescription for a 5ARI were matched to non-5ARI users. Matching was done using a propensity score of selected covariates to make 96 different covariates comparable. We measured 5 additional baseline variables which may have impacted the risk of future BC diagnosis prior cystoscopy, urine cytology, urinalysis, gross hematuria episodes, and transurethral resection of a bladder lesion. Only the first period of continuous usage of 5ARIs was considered. The prespecified at-risk period for outcomes started 1 year after initiating therapy and ended at the last date of 5ARI exposure + 1 year.

RESULTS:

We identified 93,197 men who initiated 5ARI therapy (52% dutasteride, and 48% finasteride) between 2003 and 2013 and matched them 11 to men who did not start a 5ARI. The median at-risk period for the 5ARI group was 1.68 years (interquartile range 1.00, 4.27). With adjustment for the variables related to prior BC investigations there was no significant difference in BC diagnosis (hazard ratio [HR] 1.05, 95% confidence interval [CI] 0.82-1.32) during the period of 0 to <2 years of 5ARI use; however, after ≥2 years of 5ARI use, the risk of BC diagnosis was significantly lower among the 5ARI group (HR 0.82, 95% CI 0.79-0.94). In a similarly adjusted model, BC mortality was lower among 5ARI users, but no longer statistically significant (HR 0.82, 95% CI 0.65, 1.02). When stratified by type of 5ARI, finasteride significantly reduced the risk of BC diagnosis after ≥2 years of continuous use (HR 0.86, 95% CI 0.76, 0.96); however, dutasteride did not (HR 0.92, 95% CI 0.83, 1.03).

CONCLUSIONS:

In a large cohort of men, the use of a 5ARI was associated with a significantly decreased the risk of BC diagnosis after more than 2 years of continuous therapy.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Hiperplasia Prostática / Neoplasias de la Vejiga Urinaria Límite: Humans / Male País/Región como asunto: America do norte Idioma: En Revista: Urol Oncol Asunto de la revista: NEOPLASIAS / UROLOGIA Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Hiperplasia Prostática / Neoplasias de la Vejiga Urinaria Límite: Humans / Male País/Región como asunto: America do norte Idioma: En Revista: Urol Oncol Asunto de la revista: NEOPLASIAS / UROLOGIA Año: 2023 Tipo del documento: Article
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