The long-term effect of doxazosin, finasteride, and combination therapy on the clinical progression of benign prostatic hyperplasia
- PMID: 14681504
- DOI: 10.1056/NEJMoa030656
The long-term effect of doxazosin, finasteride, and combination therapy on the clinical progression of benign prostatic hyperplasia
Abstract
Background: Benign prostatic hyperplasia is commonly treated with alpha-adrenergic-receptor antagonists (alpha-blockers) or 5alpha-reductase inhibitors. The long-term effect of these drugs, singly or combined, on the risk of clinical progression is unknown.
Methods: We conducted a long-term, double-blind trial (mean follow-up, 4.5 years) involving 3047 men to compare the effects of placebo, doxazosin, finasteride, and combination therapy on measures of the clinical progression of benign prostatic hyperplasia.
Results: The risk of overall clinical progression--defined as an increase above base line of at least 4 points in the American Urological Association symptom score, acute urinary retention, urinary incontinence, renal insufficiency, or recurrent urinary tract infection--was significantly reduced by doxazosin (39 percent risk reduction, P<0.001) and finasteride (34 percent risk reduction, P=0.002), as compared with placebo. The reduction in risk associated with combination therapy (66 percent for the comparison with placebo, P<0.001) was significantly greater than that associated with doxazosin (P<0.001) or finasteride (P<0.001) alone. The risks of acute urinary retention and the need for invasive therapy were significantly reduced by combination therapy (P<0.001) and finasteride (P<0.001) but not by doxazosin. Doxazosin (P<0.001), finasteride (P=0.001), and combination therapy (P<0.001) each resulted in significant improvement in symptom scores, with combination therapy being superior to both doxazosin (P=0.006) and finasteride (P<0.001) alone.
Conclusions: Long-term combination therapy with doxazosin and finasteride was safe and reduced the risk of overall clinical progression of benign prostatic hyperplasia significantly more than did treatment with either drug alone. Combination therapy and finasteride alone reduced the long-term risk of acute urinary retention and the need for invasive therapy.
Copyright 2003 Massachusetts Medical Society
Comment in
-
Medical management of benign prostatic hyperplasia--are two drugs better than one?N Engl J Med. 2003 Dec 18;349(25):2449-51. doi: 10.1056/NEJMe038154. N Engl J Med. 2003. PMID: 14681512 No abstract available.
-
Finasteride in benign prostatic hyperplasia.N Engl J Med. 2004 Mar 25;350(13):1359-61; author reply 1359-61. doi: 10.1056/NEJMc045013. N Engl J Med. 2004. PMID: 15044649 No abstract available.
-
Finasteride in benign prostatic hyperplasia.N Engl J Med. 2004 Mar 25;350(13):1359-61; author reply 1359-61. N Engl J Med. 2004. PMID: 15049034 No abstract available.
-
Doxazosin plus finasteride reduced clinical progression of benign prostatic hyperplasia more than either drug used alone.ACP J Club. 2004 Jul-Aug;141(1):20. ACP J Club. 2004. PMID: 15230568 No abstract available.
-
The medical therapy of prostatic symptoms trial.Curr Urol Rep. 2004 Aug;5(4):249-50. doi: 10.1007/s11934-004-0046-2. Curr Urol Rep. 2004. PMID: 15260923 No abstract available.
Publication types
MeSH terms
Substances
Grants and funding
- U01 DK-49880/DK/NIDDK NIH HHS/United States
- U01 DK-49960/DK/NIDDK NIH HHS/United States
- U01 DK41418/DK/NIDDK NIH HHS/United States
- U01 DK46416/DK/NIDDK NIH HHS/United States
- U01 DK46429/DK/NIDDK NIH HHS/United States
- U01 DK46431/DK/NIDDK NIH HHS/United States
- U01 DK46437/DK/NIDDK NIH HHS/United States
- U01 DK46468/DK/NIDDK NIH HHS/United States
- U01 DK46472/DK/NIDDK NIH HHS/United States
- U01 DK49912/DK/NIDDK NIH HHS/United States
- U01 DK49951/DK/NIDDK NIH HHS/United States
- U01 DK49954/DK/NIDDK NIH HHS/United States
- U01 DK49963/DK/NIDDK NIH HHS/United States
- U01 DK49964/DK/NIDDK NIH HHS/United States
- U01 DK49971/DK/NIDDK NIH HHS/United States
- U01 DK49977/DK/NIDDK NIH HHS/United States
- U01 DK49980/DK/NIDDK NIH HHS/United States
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical