Therapeutic strategies for managing BPH progression

被引:9
作者
Fitzpatrick, John M. [1 ]
Artibani, Walter
机构
[1] Mater Hosp, Dept Surg, Dublin, Ireland
[2] Univ Padua, Urol Clin, Dept Oncol & Surg Sci, I-35100 Padua, Italy
关键词
BPH; disease progression; LUTS; 5 alpha-reductase inhibitors; TURP;
D O I
10.1016/j.eursup.2006.08.009
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
The aim of therapy for benign prostatic hyperplasia (BPH) is to improve quality of life by providing symptom relief and an increased maximum flow rate (Q(max)), as well as to reduce disease progression and the development of new morbidities. Watchful waiting can be recommended when the International Prostate Symptom Score is <= 7, that is, mild symptoms that do not interfere with daily life activities. The alpha(1)-blockers are an established therapy for BPH and onset of action is rapid, generally within 2 wk of commencing treatment. Intermediate-term benefits can be seen in an improvement in Q(max) of 10-15% and in symptom scores of 15-20%. The other main medical therapies for BPH are the 5 alpha-reductase inhibitors (5ARIs), which not only reduce symptoms and improve Q(max), but also importantly reduce prostate volume. Dutasteride, a dual 5ARI, can provide benefits in symptom score and Q(max) within 1 mo. The improvements in symptom score and Q(max) continue up to 4 yr, with stabilisation of prostate volume. In the long-term, unlike alpha(1)-blockers, 5ARIs reduce the risk of BPH progression. The risk of acute urinary retention for men taking dutasteride was reduced by 48% compared with placebo at 2 yr (p < 0.001) and the risk of BPH-related surgery by 55% (p < 0.001). The combination of an alpha(1)-blocker and a 5ARI could be considered to provide added benefits over either therapy alone. (c) 2006 European Association of Urology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:997 / 1003
页数:7
相关论文
共 42 条
[1]   Finasteride significantly reduces acute urinary retention and need for surgery in patients with symptomatic benign prostatic hyperplasia [J].
Andersen, JT ;
Nickel, JC ;
Marshall, VR ;
Schulman, CC ;
Boyle, P .
UROLOGY, 1997, 49 (06) :839-845
[3]   Alpha-blocker therapy can be withdrawn in the majority of men following initial combination therapy with the dual 5α-reductase inhibitor dutasteride [J].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
[4]   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
[5]   5-alpha reductase inhibition provides superior benefits to alpha blockade by preventing AUR and BPH-related surgery [J].
Boyle, P ;
Roehrborn, C ;
Harkaway, R ;
Logie, J ;
de la Rosette, J ;
Emberton, M .
EUROPEAN UROLOGY, 2004, 45 (05) :620-627
[6]  
Boyle P., 2003, European Urology Supplements, V2, P160, DOI 10.1016/S1569-9056(03)80634-6
[7]   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
[8]   Marked suppression of dihydrotestosterone in men with benign prostatic hyperplasia by dutasteride, a dual 5α-reductase inhibitor [J].
Clark, RV ;
Hermann, DJ ;
Cunningham, GR ;
Wilson, TH ;
Morrill, BB ;
Hobbs, S .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (05) :2179-2184
[9]   Baseline factors as predictors of clinical progression of benign prostatic hyperplasia in men treated with placebo [J].
Crawford, ED ;
Wilson, SS ;
McConnell, JD ;
Slawin, KM ;
Lieber, MC ;
Smith, JA ;
Meehan, AG ;
Bautista, OM ;
Noble, WR ;
Kusek, JW ;
Nyberg, LM ;
Roehrborn, CG .
JOURNAL OF UROLOGY, 2006, 175 (04) :1422-1426
[10]   Long-term risk of re-treatment of patients using α-blockers for lower urinary tract symptoms [J].
De La Rosette, JJMCH ;
Kortmann, BBM ;
Rossi, C ;
Sonke, GS ;
Floratos, DL ;
Kiemeney, LALM .
JOURNAL OF UROLOGY, 2002, 167 (04) :1734-1738