Specifically, the mean prostate volume in the VA trial was 37 cm3 compared with
58.6 cm3 in the finasteride registration study. Therefore, the findings of the VA study reflect the effectiveness of the evaluated medical therapies for all men with clinical BPH, whereas the findings of the finasteride registration study are relevant only to the subset of men with clinical BPH and large prostates. Figure 3 Comparison of finasteride, terazosin, and combined dosing regimens for the treatment of benign Inhibitors,research,lifescience,medical prostatic hyperplasia. Symptom scores and flow rates are expressed as adjusted means and 95% confidence intervals. (A) American Urological Association symptom … The findings of the VA study were AEB071 purchase replicated by the PREDICT13 study, which substituted the α-blocker doxazosin for terazosin. Again, the doxazosin was significantly more effective than placebo at relieving LUTS and increasing peak urinary flow rate, and finasteride was no more effective than Inhibitors,research,lifescience,medical placebo; there was Inhibitors,research,lifescience,medical no benefit of
combination therapy over α-blocker monotherapy (Figure 4). In the PREDICT study, the baseline prostate volume was 36 g, which is virtually identical to the VA study. Figure 4 The mean changes in International Prostate Symptom Score (IPSS) score and peak flow rate (PFR) between baseline and 1 year of active treatment of men randomized to placebo (PLB) and finasteride (FIN), doxazosin (DOX), or a finasteride + doxazosin (CMB) …
The Inhibitors,research,lifescience,medical VA and PREDICT studies were designed to examine the relative effectiveness of α-blockers, 5-ARIs, and the combination of these two classes of drugs for improving LUTS and BOO over a 1-year period. The Medical Therapy of Prostatic Symptoms (MTOPS) study was designed primarily to address disease Inhibitors,research,lifescience,medical progression. MTOPS examined the ability of a 5-ARI (finasteride), an α-blocker (doxazosin), and the combination of these two classes of drugs (finasteride and doxazosin) to prevent disease progression relative to placebo.14 In this randomized, placebo-controlled study Digestive enzyme enrolling 3047 men with clinical BPH, the primary endpoint was clinical BPH progression and the secondary endpoints were changes in LUTS and peak urinary flow rate. Clinical BPH progression was defined as a four-point increase in AUASS or development of acute urinary retention (AUR), renal insufficiency, urinary tract infection (UTI), or incontinence. The requirement for invasive therapy due to BPH was also captured. With a mean follow-up of 4.5 years, all treatment groups significantly decreased overall disease progression relative to placebo (Figure 5). Combination therapy was significantly more effective than monotherapy at preventing overall disease progression.