World J Mens Health.  2014 Apr;32(1):28-35.

The Efficacy and Safety of Tadalafil 5 mg Once Daily in Korean Men with Lower Urinary Tract Symptoms Suggestive of Benign Prostatic Hyperplasia: An Integrated Analysis

Affiliations
  • 1Department of Urology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • 2Department of Urology, Seoul National University Hospital, Seoul, Korea.
  • 3Department of Urology, Pusan National University Hospital, Medical Research Institute, Pusan National University School of Medicine, Busan, Korea.
  • 4Eli Lilly Korea, Seoul, Korea. won_ji_eon@lilly.com
  • 5Eli Lilly Japan K.K., Kobe, Japan.
  • 6Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, USA.

Abstract

PURPOSE
This post hoc integrated analysis assessed the efficacy and safety of tadalafil 5 mg once daily in a large Korean population with lower urinary tract symptoms suggestive of benign prostatic hyperplasia (BPH-LUTS).
MATERIALS AND METHODS
Individual Korean participant data were integrated from three 12-week, randomized, double-blind, placebo-controlled studies in Asian men with BPH-LUTS, wherein 177 Korean men received placebo and 177 received tadalafil 5 mg once daily. The primary objective was to compare the change from baseline to week 12 in total International Prostate Symptom Score (IPSS) after treatment with tadalafil versus placebo.
RESULTS
A significantly greater improvement (p<0.001) in total IPSS from baseline to week 12 was observed for tadalafil compared to placebo (least squares mean: tadalafil=-5.97; placebo=-3.94 ). Total IPSS at weeks 4 and 12, IPSS voiding and storage subscores at weeks 4, 8, and 12, and IPSS quality of life index at weeks 8 and 12 were also significantly improved (p<0.05) for tadalafil compared to placebo. There was significant improvement (p<0.001) in the patient global Impression of improvement responses and numerical improvement in the clinician global impression of improvement responses with tadalafil compared to placebo. There were no significant treatment differences for peak urine flow rate or postvoid residual volume . Few participants had treatment-emergent adverse events and there were no unexpected safety findings.
CONCLUSIONS
This integrated analysis of three randomized, placebo-controlled Asian studies confirmed tadalafil 5 mg once daily as an efficacious and well-tolerated treatment for Korean men with BPH-LUTS.

Keyword

Benign prostatic hyperplasia; Korean; Lower urinary tract symptoms; Phosphodiesterase type 5 inhibitors; Tadalafil

MeSH Terms

Asian Continental Ancestry Group
Humans
Lower Urinary Tract Symptoms*
Male
Phosphodiesterase 5 Inhibitors
Prostate
Prostatic Hyperplasia*
Quality of Life
Residual Volume
Tadalafil
Phosphodiesterase 5 Inhibitors

Figure

  • Fig. 1 Disposition of participants. aNumber of participants randomized.

  • Fig. 2 Change from the baseline to weeks 4, 8, and 12 in total IPSS in Korean men with BPH-LUTS receiving placebo or tadalafil 5 mg. Data were analyzed using mixed-effects model repeated measures analysis and represent LS mean change±SE. IPSS: International Prostate Symptom Score, LS: least squares, SE: standard error, BPH-LUTS: lower urinary tract symptoms suggestive of benign prostatic hyperplasia. *p<0.05. **p<0.001.


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