Literature DB >> 23375241

Systematic review of combination drug therapy for non-neurogenic male lower urinary tract symptoms.

Claudius Füllhase1, Christopher Chapple, Jean-Nicolas Cornu, Cosimo De Nunzio, Christian Gratzke, Steven A Kaplan, Michael Marberger, Francesco Montorsi, Giacomo Novara, Matthias Oelke, Hartmut Porst, Claus Roehrborn, Christian Stief, Kevin T McVary.   

Abstract

BACKGROUND: Several drugs are approved for the treatment of lower urinary tract symptoms (LUTS) in men, but these are mostly used by clinicians as monotherapies. The combination of different compounds, each of which targets a different aspect of LUTS, seems appealing. However, only few clinical trials have evaluated the effects of combination therapies.
OBJECTIVE: This systematic review analyzes the efficacy and adverse events of combination therapies for male LUTS. EVIDENCE ACQUISITION: PubMed and Cochrane databases were used to identify clinical trials and meta-analyses on male LUTS combination therapy. The search was restricted to studies of level of evidence ≥ 1b. A total of 49 papers published between January 1988 and March 2012 were identified. EVIDENCE SYNTHESIS: The α1-adrenoceptor antagonist (α1-blocker)/5α-reductase inhibitor (5-ARI) combination provides the most data. This combination seems to be more efficacious in terms of several outcome variables in patients whose prostate volume is between 30 ml and 40 ml when treatment is maintained for >1 yr; when given for <1 yr, α1-blockers alone are just as effective. The combination of α1-blocker/5-ARI shows a slightly increased rate of adverse events. It remains unknown whether its safety and superiority over either drug as monotherapy are sustained after >6 yr. The α1-blocker/muscarinic receptor antagonist (antimuscarinic) combination was most frequently assessed as an add-on therapy to already existing α1-blocker therapy. Inconsistent data derive from heterogeneous study populations and different study designs. Currently, the α1-blocker/antimuscarinic combination appears to be a second-line add-on for patients with insufficient symptom relief after monotherapy. The combination seems to be safe in men with postvoid residual <200 ml. However, there are no trials >4 mo concerning safety and efficacy of this combination. The α1-blocker/phosphodiesterase type 5 inhibitor combination is a new treatment option with only preliminary reports. More studies are needed before definitive conclusions can be drawn.
CONCLUSIONS: An α1-blocker/5-ARI combination is beneficial for patients whose prostate volume is between 30 ml and 40 ml when medical treatment is intended for >1 yr. Based on short-term follow-up studies, add-on of antimuscarinics to α1-blockers is an option when postvoid residual is <200 ml.
Copyright © 2013 European Association of Urology. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  5α-reductase inhibitors; Adrenergic α(1)-receptor antagonists; Lower urinary tract symptoms; Muscarinic antagonists; Prostatic hyperplasia

Mesh:

Substances:

Year:  2013        PMID: 23375241     DOI: 10.1016/j.eururo.2013.01.018

Source DB:  PubMed          Journal:  Eur Urol        ISSN: 0302-2838            Impact factor:   20.096


  27 in total

1.  Smooth muscle contraction and growth of stromal cells in the human prostate are both inhibited by the Src family kinase inhibitors, AZM475271 and PP2.

Authors:  Yiming Wang; Christian Gratzke; Alexander Tamalunas; Beata Rutz; Anna Ciotkowska; Frank Strittmatter; Annika Herlemann; Sophie Janich; Raphaela Waidelich; Chunxiao Liu; Christian G Stief; Martin Hennenberg
Journal:  Br J Pharmacol       Date:  2016-11-01       Impact factor: 8.739

2.  Antidepression medication improves quality of life in elderly patients with benign prostatic hyperplasia and depression.

Authors:  Lina Ma; Xiaoling Zhao; Huizhen Liu; Hong Zhu; Wei Yang; Yuying Qian; Jieyu Wang; Ming Feng; Yun Li
Journal:  Int J Clin Exp Med       Date:  2015-03-15

Review 3.  Targeting phenotypic heterogeneity in benign prostatic hyperplasia.

Authors:  Douglas W Strand; Daniel N Costa; Franto Francis; William A Ricke; Claus G Roehrborn
Journal:  Differentiation       Date:  2017-08-04       Impact factor: 3.880

Review 4.  The role of inflammation in lower urinary tract symptoms (LUTS) due to benign prostatic hyperplasia (BPH) and its potential impact on medical therapy.

Authors:  Vincenzo Ficarra; Marta Rossanese; Michele Zazzara; Gianluca Giannarini; Maria Abbinante; Riccardo Bartoletti; Vincenzo Mirone; Francesco Scaglione
Journal:  Curr Urol Rep       Date:  2014-12       Impact factor: 3.092

Review 5.  Treatment of lower urinary tract symptoms in benign prostatic hypertrophy with α-blockers.

Authors:  Mathieos Belayneh; Christina Korownyk
Journal:  Can Fam Physician       Date:  2016-09       Impact factor: 3.275

6.  Inhibition of human prostate smooth muscle contraction by the LIM kinase inhibitors, SR7826 and LIMKi3.

Authors:  Qingfeng Yu; Christian Gratzke; Yiming Wang; Annika Herlemann; Christian Maximilian Sterr; Beata Rutz; Anna Ciotkowska; Xiaolong Wang; Frank Strittmatter; Christian G Stief; Martin Hennenberg
Journal:  Br J Pharmacol       Date:  2018-04-29       Impact factor: 8.739

7.  Mirabegron for male lower urinary tract symptoms.

Authors:  Oscar Suarez; David Osborn; Melissa Kaufman; W Stuart Reynolds; Roger Dmochowski
Journal:  Curr Urol Rep       Date:  2013-12       Impact factor: 3.092

8.  Effect of Onabotulinum Toxin A on Substance P and Receptor Neurokinin 1 in the Rat Ventral Prostate.

Authors:  Omer Onur Cakir; Carol A Podlasek; Douglas Wood; Kevin E McKenna; Kevin T McVary
Journal:  Andrology (Los Angel)       Date:  2015-03-28

9.  Actual medical management of lower urinary tract symptoms related to benign prostatic hyperplasia: temporal trends of prescription and hospitalization rates over 5 years in a large population of Italian men.

Authors:  Luca Cindolo; Luisella Pirozzi; Caterina Fanizza; Marilena Romero; Petros Sountoulides; Claus G Roehrborn; Vincenzo Mirone; Luigi Schips
Journal:  Int Urol Nephrol       Date:  2013-10-18       Impact factor: 2.370

10.  The STK16 inhibitor STK16-IN-1 inhibits non-adrenergic and non-neurogenic smooth muscle contractions in the human prostate and the human male detrusor.

Authors:  Bingsheng Li; Xiaolong Wang; Beata Rutz; Ruixiao Wang; Alexander Tamalunas; Frank Strittmatter; Raphaela Waidelich; Christian G Stief; Martin Hennenberg
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2019-12-23       Impact factor: 3.000

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