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Silodosin in the treatment of benign prostatic hyperplasia

Authors Maxime Rossi, Thierry Roumeguère

Published 27 October 2010 Volume 2010:4 Pages 291—297

DOI https://doi.org/10.2147/DDDT.S10428

Review by Single-blind

Peer reviewer comments 5

Maxime Rossi, Thierry Roumeguère
Department of Urology, Erasme Hospital, University Clinics of Brussels, ULB, Brussels, Belgium

Abstract: Benign prostatic hyperplasia (BPH)-associated lower urinary tract symptoms (LUTS) are highly prevalent in older men. Medical therapy is the first-line treatment for LUTS due to BPH. Alpha-adrenergic receptor blockers remain one of the mainstays in the treatment of male LUTS and clinical BPH. They exhibit early onset of efficacy with regard to both symptoms and flow rate improvement, and this is clearly demonstrated in placebo-controlled trials with extensions out to five years. These agents have been shown to prevent symptomatic progression of the disease. The aim of this article is to offer a critical review of the current literature on silodosin, formerly known as KMD-3213, a novel alpha-blocker with unprecedented selectivity for a1A-adrenergic receptors, as compared with both a1B- and a1D -adrenoceptors, exceeding the selectivity of all currently used a1-blockers, and with clinically promising effects.

Keywords: silodosin, a1A- blockers, lower urinary tract symptoms, benign prostatic hyperplasia, uroselectivity

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