Korean J Urol.  2014 May;55(5):335-340. 10.4111/kju.2014.55.5.335.

Efficacy and Safety of the Selective alpha1A-Adrenoceptor Blocker Silodosin for Severe Lower Urinary Tract Symptoms Associated With Benign Prostatic Hyperplasia: A Prospective, Single-Open-Label, Multicenter Study in Korea

Affiliations
  • 1Department of Urology, Yeungnam University Hospital, Daegu, Korea.
  • 2Department of Urology, Hallym University Medical Center, Seoul, Korea.
  • 3Department of Urology, Pusan National University Hospital, Busan, Korea.
  • 4Department of Urology, Seoul National University Hospital, Seoul, Korea.
  • 5Department of Urology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • 6Department of Urology, Seoul St. Mary's Hospital, Seoul, Korea.
  • 7Department of Urology, Korea University Guro Hospital, Seoul, Korea.
  • 8Department of Urology, Chonbuk National University Medical School, Jeonju, Korea.
  • 9Institute for Medical Sciences, Chonbuk National University, Jeonju, Korea.
  • 10Biomedical Research Institute and Clinical Trial Center of Medical Device of Chonbuk National University Hospital, Jeonju, Korea.
  • 11Department of Urology, Asan Medical Center, Seoul, Korea.
  • 12Department of Urology, Chonnam National University Medical School, Gwangju, Korea. kpark@chonnam.ac.kr

Abstract

PURPOSE
To evaluate the efficacy and safety of silodosin 8 mg once daily in a 12-week treatment of subjects with severe lower urinary tract symptoms (LUTS) associated with benign prostatic hyperplasia (BPH).
MATERIALS AND METHODS
A total of 100 subjects from 10 urology centers in Korea were included in this study. The inclusion criteria were as follows: age > or =50 years, International Prostate Symptom Score (IPSS) > or =20, quality of life (QoL) score > or =3, urine volume > or =120 mL and maximal urinary flow rate (Qmax) <15 mL/s, and postvoid residual volume (PVR) <100 mL. We assessed the improvement of LUTS with change in IPSS, QoL score, Qmax, PVR, and adverse events at baseline and 4 and 12 weeks after treatment with silodosin 8 mg once daily.
RESULTS
The IPSS values were 23.27+/-3.34, 15.89+/-6.26, and 13.80+/-6.31 at baseline, 4, and 12 weeks, respectively, with significant improvements (p<0.0001, p=0.0214, respectively). QoL scores were 4.44+/-0.85, 3.38+/-1.20, and 3.04+/-1.20 at baseline, 4, and 12 weeks, respectively, and the differences were statistically significant (p<0.0001). There was a significant difference in Qmax between baseline and 12 weeks (p<0.0001) but not in PVR (p=0.9404) during the clinical trial. The most frequent adverse event in this study was ejaculation failure with 13 cases. However, no subject dropped out because of ejaculation failure, and in 12 of the 13 cases it was fully resolved without further treatment.
CONCLUSIONS
Silodosin 8 mg once daily may be effective and safe in Korean patients with severe LUTS associated with BPH.

Keyword

alpha1A-Adrenoceptor antagonis; Benign prostatic hyperplasia; Lower urinary tract symptoms; Selective; Silodosin

MeSH Terms

Ejaculation
Humans
Korea
Lower Urinary Tract Symptoms*
Male
Prospective Studies*
Prostate
Prostatic Hyperplasia*
Quality of Life
Residual Volume
Urology

Figure

  • FIG. 1 Change in efficacy variables. The p-values are computed from paired t-test. IPSS, International Prostate Symptom Score; QoL, quality of life; Qmax, maximal urinary flow rate; PVR, postvoid residual volume.


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