Dutasteride reduces prostate size and prostate specific antigen in older hypogonadal men with benign prostatic hyperplasia undergoing testosterone replacement therapy

J Urol. 2011 Jul;186(1):191-7. doi: 10.1016/j.juro.2011.03.026. Epub 2011 May 14.

Abstract

Purpose: Benign prostatic hyperplasia and hypogonadism are common disorders in aging men. There is concern that androgen replacement in older men may increase prostate size and symptoms of benign prostatic hyperplasia. We examined whether combining dutasteride, which inhibits testosterone to dihydrotestosterone conversion, with testosterone treatment in older hypogonadal men with benign prostatic hyperplasia reduces androgenic stimulation of the prostate compared to testosterone alone.

Materials and methods: We conducted a double-blind, placebo controlled trial of 53 men 51 to 82 years old with symptomatic benign prostatic hyperplasia, prostate volume 30 cc or greater and serum total testosterone less than 280 ng/dl (less than 9.7 nmol/l). Subjects were randomized to daily transdermal 1% T gel plus oral placebo or dutasteride for 6 months. Testosterone dosing was adjusted to a serum testosterone of 500 to 1,000 ng/dl. The primary outcomes were prostate volume measured by magnetic resonance imaging, serum prostate specific antigen and androgen levels.

Results: A total of 46 subjects completed all procedures. Serum testosterone increased similarly into the mid-normal range in both groups. Serum dihydrotestosterone increased in the testosterone only but decreased in the testosterone plus dutasteride group. In the testosterone plus dutasteride group prostate volume and prostate specific antigen (mean ± SEM) decreased 12% ± 2.5% and 35% ± 5%, respectively, compared to the testosterone only group in which prostate volume and prostate specific antigen increased 7.5% ± 3.3% and 19% ± 7% (p = 0.03 and p = 0.008), respectively, after 6 months of treatment. Prostate symptom scores improved in both groups.

Conclusions: Combined treatment with testosterone plus dutasteride reduces prostate volume and prostate specific antigen compared to testosterone only. Coadministration of a 5α-reductase inhibitor with testosterone appears to spare the prostate from androgenic stimulation during testosterone replacement in older, hypogonadal men with symptomatic benign prostatic hyperplasia.

Trial registration: ClinicalTrials.gov NCT00194675.

Publication types

  • Comparative Study
  • Randomized Controlled Trial
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • 5-alpha Reductase Inhibitors / pharmacology*
  • 5-alpha Reductase Inhibitors / therapeutic use
  • Aged
  • Aged, 80 and over
  • Androgens / pharmacology*
  • Androgens / therapeutic use
  • Azasteroids / pharmacology*
  • Azasteroids / therapeutic use
  • Double-Blind Method
  • Drug Therapy, Combination
  • Dutasteride
  • Hormone Replacement Therapy
  • Humans
  • Hypogonadism / blood*
  • Hypogonadism / drug therapy
  • Hypogonadism / pathology*
  • Male
  • Middle Aged
  • Organ Size / drug effects
  • Prostate / drug effects*
  • Prostate / pathology*
  • Prostate-Specific Antigen / blood*
  • Prostate-Specific Antigen / drug effects*
  • Prostatic Hyperplasia / blood*
  • Prostatic Hyperplasia / drug therapy
  • Prostatic Hyperplasia / pathology*
  • Testosterone / pharmacology*
  • Testosterone / therapeutic use

Substances

  • 5-alpha Reductase Inhibitors
  • Androgens
  • Azasteroids
  • Testosterone
  • Prostate-Specific Antigen
  • Dutasteride

Associated data

  • ClinicalTrials.gov/NCT00194675