The long-term effect of doxazosin, finasteride, and combination therapy on the clinical progression of benign prostatic hyperplasia

被引:1386
作者
McConnell, JD
Roehrborn, CG
Bautista, OM
Andriole, GL
Dixon, CM
Kusek, JW
Lepor, H
McVary, KT
Nyberg, LM
Clarke, HS
Crawford, ED
Diokno, A
Foley, JP
Foster, HE
Jacobs, SC
Kaplan, SA
Kreder, KJ
Lieber, MM
Lucia, MS
Miller, GJ
Menon, M
Milam, DF
Ramsdell, JW
Schenkman, NS
Slawin, KM
Smith, JA
Kusek, JW
Nyberg, LM
Briggs, JP
McConnell, JD
Crawford, ED
Homan, K
Donohue, R
Parker, D
Easterday, K
Robertson, K
Kaplan, S
Wentland, M
Hardy, L
Roehrborn, C
Ahrens, A
McConnell, J
Hall, D
Cutts, D
Carter, S
Waldrep, K
Schenkman, N
Sanetrik, K
Sihelnik, S
Zorn, B
机构
[1] Univ Texas, SW Med Ctr, Dallas, TX 75390 USA
[2] George Washington Univ, Rockville, MD USA
[3] Washington Univ, St Louis, MO USA
[4] NYU, New York, NY USA
[5] NIDDKD, Bethesda, MD 20892 USA
[6] Northwestern Univ, Chicago, IL 60611 USA
[7] Emory Univ, Atlanta, GA 30322 USA
[8] Univ Colorado, Hlth Sci Ctr, Denver, CO USA
[9] William Beaumont Hosp, Royal Oak, MI 48072 USA
[10] Brooke Army Med Ctr, Ft Sam Houston, TX 78234 USA
[11] Yale Univ, New Haven, CT USA
[12] Univ Maryland, Baltimore, MD 21201 USA
[13] New York Presbyterian Hosp, New York, NY USA
[14] Univ Iowa, Iowa City, IA USA
[15] Mayo Clin, Rochester, MN USA
[16] Henry Ford Hosp, Detroit, MI 48202 USA
[17] Vanderbilt Univ, Nashville, TN USA
[18] Univ Calif San Diego, San Diego, CA 92103 USA
[19] Walter Reed Army Med Ctr, Washington, DC 20307 USA
[20] Baylor Coll Med, Houston, TX 77030 USA
关键词
D O I
10.1056/NEJMoa030656
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Benign prostatic hyperplasia is commonly treated with alpha-adrenergic-receptor antagonists (alpha-blockers) or 5(alpha)-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.
引用
收藏
页码:2387 / 2398
页数:12
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