The role of combination medical therapy in benign prostatic hyperplasia

被引:37
作者
Greco, K. A. [1 ]
McVary, K. T. [1 ]
机构
[1] Northwestern Univ, Dept Urol, Feinberg Sch Med, Chicago, IL 60611 USA
关键词
D O I
10.1038/ijir.2008.51
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
To review key trials of monotherapy and combination therapy of a1-adrenergic receptor antagonists (alpha(1)-ARAs), 5a-reductase inhibitors (5aRIs) and anti-muscarinic agents in the treatment of lower urinary tract symptoms (LUTS) associated with benign prostatic hyperplasia (BPH). To assess the safety and efficacy of combination therapies for LUTS associated with BPH, a search of the MEDLINE and Cochrane databases (1976-2008) was conducted for relevant trials and reviews using the terms benign prostatic hyperplasia, lower urinary tract symptoms, alpha(1)-adrenergic receptor antagonists, 5a-reductase inhibitors, anti-muscarinics, anticholinergics, combination therapy, alfuzosin, doxazosin, tamsulosin, terazosin, dutasteride, finasteride, tolterodine, flavoxate, propiverine, oxybutynin, erectile dysfunction, sildenafil, vardenafil and tadalafil. Data from the Medical Therapy of Prostatic Symptoms (MTOPS) study indicated a role for long-term use of a1-ARAs and 5aRIs in combination. In the MTOPS study, combination therapy with the alpha(1)-ARA doxazosin and the 5aRI finasteride was significantly more effective than either component alone in reducing symptoms (P = 0.006 vs doxazosin monotherapy; P < 0.001 vs finasteride monotherapy) and in lowering the rate of clinical progression (P < 0.001 vs either monotherapy). These findings were confirmed by the 2-year preliminary results of the Combination of Avodart and Tamsulosin study. In this study, combination therapy of the alpha(1)-ARA tamsulosin and the 5 alpha RI dutasteride resulted in a significantly greater decrease in International Prostate Symptom Score (IPSS) when compared with either monotherapy. Several recent trials have studied the efficacy of combining alpha(1)-ARAs and anti-muscarinic agents in the treatment of BPH. These studies have found this combination to result in statistically significant benefits in quality of life scores, patient satisfaction, urinary frequency, storage symptoms and IPSS scores. Studies have not shown an increased risk of urinary retention associated with the use of anti-muscarinics in a highly select cohort of men with BPH. The available data suggest that combination therapy can be beneficial in the treatment of BPH and associated LUTS. The greatest efficacy for the alpha(1)-ARA and 5 alpha RI combination was shown in patients with larger prostate size and more severe symptoms. The combination of alpha(1)-ARAs and 5aRIs appears to prevent disease progression in these patients. The combination of alpha(1)-ARAs with anti-muscarinic agents is useful for relieving symptoms of bladder outlet obstruction and detrusor overactivity. Theoretic concerns regarding the risk of acute urinary retention have been refuted in several recent clinical trials; however, it must be noted that the patients in these trials were a highly select cohort of men. Men with overactive bladder and BPH who are not receiving adequate alleviation of symptoms from the first-line alpha(1)-ARAs may benefit from the addition of an anti-muscarinic agent.
引用
收藏
页码:S33 / S43
页数:11
相关论文
共 49 条
[1]   Safety and tolerability of tolterodine for the treatment of overactive bladder in men with bladder outlet obstruction [J].
Abrams, P ;
Kaplan, S ;
Gans, HJD ;
Millard, R .
JOURNAL OF UROLOGY, 2006, 175 (03) :999-1004
[2]  
*AM UR ASS, GUID MAN BEN PROST H
[3]   Combination treatment with an α-blocker plus an anticholinergic for bladder outlet obstruction:: A prospective, randomized, controlled study [J].
Athanasopoulos, A ;
Gyftopoulos, K ;
Giannitsas, K ;
Fisfis, J ;
Perimenis, P ;
Barbalias, G .
JOURNAL OF UROLOGY, 2003, 169 (06) :2253-2256
[4]   Alpha-blocker therapy can be withdrawn in the majority of men following initial combination therapy with the dual 5α-reductase inhibitor dutasteride [J].
Barkin, J ;
Guimaraes, M ;
Jacobi, G ;
Pushkar, D ;
Taylor, S ;
van Vierssen Trip, OB .
EUROPEAN UROLOGY, 2003, 44 (04) :461-466
[5]   THE AMERICAN-UROLOGICAL-ASSOCIATION SYMPTOM INDEX FOR BENIGN PROSTATIC HYPERPLASIA [J].
BARRY, MJ ;
FOWLER, FJ ;
OLEARY, MP ;
BRUSKEWITZ, RC ;
HOLTGREWE, HL ;
MEBUST, WK ;
COCKETT, ATK ;
BLAIVAS, JG ;
WEIN, AJ .
JOURNAL OF UROLOGY, 1992, 148 (05) :1549-1557
[6]   THE DEVELOPMENT OF HUMAN BENIGN PROSTATIC HYPERPLASIA WITH AGE [J].
BERRY, SJ ;
COFFEY, DS ;
WALSH, PC ;
EWING, LL .
JOURNAL OF UROLOGY, 1984, 132 (03) :474-479
[7]   The role of anticholinergics in men with lower urinary tract symptoms suggestive of benign prostatic hyperplasia: a systematic review and meta-analysis [J].
Blake-James, Benedict T. ;
Rashidian, Arash ;
Ikeda, Youko ;
Emberton, Mark .
BJU INTERNATIONAL, 2007, 99 (01) :85-96
[8]   Prostate volume predicts outcome of treatment of benign prostatic hyperplasia with finasteride: Meta-analysis of randomized clinical trials [J].
Boyle, P ;
Gould, AL ;
Roehrborn, CG .
UROLOGY, 1996, 48 (03) :398-405
[9]   The fear of prostate cancer in men with lower urinary tract symptoms: should symptomatic men be screened? [J].
Brown, CT ;
O'Flynn, E ;
Van der Meulen, J ;
Newman, S ;
Mundy, AR ;
Emberton, M .
BJU INTERNATIONAL, 2003, 91 (01) :30-32
[10]   ADRENERGIC AND CHOLINERGIC RECEPTORS IN HUMAN PROSTATE, PROSTATIC CAPSULE AND BLADDER NECK [J].
CAINE, M ;
RAZ, S ;
ZEIGLER, M .
BRITISH JOURNAL OF UROLOGY, 1975, 47 (02) :193-202