The Effects of Combination Therapy with Dutasteride and Tamsulosin on Clinical Outcomes in Men with Symptomatic Benign Prostatic Hyperplasia: 4-Year Results from the CombAT Study

被引:533
作者
Roehrborn, Claus G. [1 ]
Siami, Paul [2 ]
Barkin, Jack [3 ]
Damiao, Ronaldo [4 ]
Major-Walker, Kim [5 ]
Nandy, Indrani [5 ]
Morrill, Betsy B. [5 ]
Gagnier, R. Paul [5 ]
Montorsi, Francesco [6 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Urol, Dallas, TX 75390 USA
[2] Deaconess Clin, Evansville, IN USA
[3] Univ Toronto, Dept Urol, Toronto, ON, Canada
[4] State Univ Rio Janeiro, Dept Urol, Rio De Janeiro, Brazil
[5] GlaxoSmithKline Inc, Res & Dev, Res Triangle Pk, NC USA
[6] Univ Vita Salute San Raffaele, Dept Urol, Milan, Italy
关键词
Benign prostatic hyperplasia; Combination drug therapy; Dutasteride; Lower urinary tract symptoms; Prostate; Surgery; Tamsulosin; Urinary retention; ACUTE URINARY RETENTION; FINASTERIDE; ENLARGEMENT; PROGRESSION; INHIBITOR; EFFICACY; ANTIGEN; PLACEBO; SAFETY; NEED;
D O I
10.1016/j.eururo.2009.09.035
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
Background: Combination therapy with dutasteride and tamsulosin provides significantly greater benefit than either monotherapy for various patient-reported outcomes in men with moderate-to-severe lower urinary tract symptoms (LUTS) due to benign prostatic hyperplasia (BPH) and prostatic enlargement. Objective: To investigate whether combination therapy is more effective than either monotherapy in reducing the relative risk for acute urinary retention (AUR), BPH-related surgery, and BPH clinical progression over 4 yr in men at increased risk of progression. Design, setting, and participants: The Combination of Avodart (R) and Tamsulosin (CombAT) study was a 4-yr, multicenter, randomised, double-blind, parallel-group study in 4844 men >= 50 yr of age with a clinical diagnosis of BPH, International Prostate Symptom Score >= 12, prostate volume >= 30 cm(3), prostate-specific antigen 1.5-10 ng/ml, and maximum urinary flow rate (Q(max)) >5 and <= 15 ml/s with minimum voided volume >= 125 ml. Intervention: Oral daily tamsulosin, 0.4 mg; dutasteride, 0.5 mg; or a combination of both. Measurements: The 4-yr primary end point was time to first AUR or BPH-related surgery. Secondary end points included BPH clinical progression, symptoms, Q(max), prostate volume, safety, and tolerability. Results and limitations: Combination therapy was significantly superior to tamsulosin monotherapy but not dutasteride monotherapy at reducing the relative risk of AUR or BPH-related surgery. Combination therapy was also significantly superior to both monotherapies at reducing the relative risk of BPH clinical progression. Combination therapy provided significantly greater symptom benefit than either monotherapy at 4 yr. Safety and tolerability of combination therapy was consistent with previous experience with dutasteride and tamsulosin monotherapies, with the exception of an imbalance in the composite term of cardiac failure among the three study arms. The lack of placebo control is a study limitation. Conclusions: The 4-yr CombAT data provide support for the long-term use of dutasteride and tamsulosin combination therapy in men with moderate-to-severe LUTS due to BPH and prostatic enlargement. Clinicaltrials.gov identifier: NCT00090103 (http://www.clinicaltrials.gov/ct2/show/NCT00090103). (C) 2009 European Association of Urology. Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:123 / 131
页数:9
相关论文
共 14 条
[1]   Intraloperative floppy-iris syndrome associated with α1-adrenoreceptors -: Comparison of tamsulosin and alfuzosin [J].
Blouin, Marie-Claude ;
Blouin, Julie ;
Perreault, Sylvie ;
Lapointe, Andre ;
Dragomir, Alice .
JOURNAL OF CATARACT AND REFRACTIVE SURGERY, 2007, 33 (07) :1227-1234
[2]   Efficacy and safety of long-term treatment with the dual 5α-reductase inhibitor dutasteride in men with symptomatic benign prostatic hyperplasia [J].
Debruyne, F ;
Barkin, J ;
van Erps, P ;
Reis, M ;
Tammela, TLJ ;
Roehrborn, C .
EUROPEAN UROLOGY, 2004, 46 (04) :488-495
[3]   Benign prostatic hyperplasia: A progressive disease of aging men [J].
Emberton, M ;
Andriole, GL ;
de la Rosette, J ;
Djavan, B ;
Hoefner, K ;
Navarrete, RV ;
Nordling, J ;
Roehrborn, C ;
Schulman, C ;
Teillac, P ;
Tubaro, A ;
Nickel, JC .
UROLOGY, 2003, 61 (02) :267-273
[4]   Progression of benign prostatic hyperplasia: systematic review of the placebo arms of clinical trials [J].
Emberton, Mark ;
Fitzpatrick, John M. ;
Garcia-Losa, Manuel ;
Qizilbash, Nawab ;
Djavan, Bob .
BJU INTERNATIONAL, 2008, 102 (08) :981-986
[5]   Natural history of benign prostatic hyperplasia [J].
Jacobsen, SJ ;
Girman, CJ ;
Lieber, MM .
UROLOGY, 2001, 58 (6A) :5-16
[6]   The long-term outcome of medical therapy for BPH [J].
Madersbacher, Stephan ;
Marszalek, Martin ;
Lackner, Jakob ;
Berger, Peter ;
Schatzl, Georg .
EUROPEAN UROLOGY, 2007, 51 (06) :1522-1533
[7]   The effect of finasteride on the risk of acute urinary retention and the need for surgical treatment among men with benign prostatic hyperplasia [J].
McConnell, JD ;
Bruskewitz, R ;
Walsh, P ;
Andriole, G ;
Lieber, M ;
Holtgrewe, HL ;
Albertsen, P ;
Roehrborn, CG ;
Nickel, JC ;
Wang, DZ ;
Taylor, AM ;
Waldstreicher, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 338 (09) :557-563
[8]   The long-term effect of doxazosin, finasteride, and combination therapy on the clinical progression of benign prostatic hyperplasia [J].
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 .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (25) :2387-2398
[9]   Serum prostate-specific antigen and prostate volume predict long-term chances in symptoms and flow rate: Results of a four-year, randomized trial comparing finasteride versus placebo [J].
Roehrborn, CG ;
Boyle, P ;
Bergner, D ;
Gray, T ;
Gittelman, M ;
Shown, T ;
Melman, A ;
Bracken, RB ;
White, RD ;
Taylor, A ;
Wang, D ;
Waldstreicher, J .
UROLOGY, 1999, 54 (04) :662-669
[10]   Serum prostate-specific antigen concentration is a powerful predictor of acute urinary retention and need for surgery in men with clinical benign prostatic hyperplasia [J].
Roehrborn, CG ;
McConnell, JD ;
Lieber, M ;
Kaplan, S ;
Geller, J ;
Malek, GH ;
Castellanos, R ;
Coffield, S ;
Saltzman, B ;
Resnick, M ;
Cook, TJ ;
Waldstreicher, J .
UROLOGY, 1999, 53 (03) :473-480