Premier Medical Group of the Hudson Valley, Poughkeepsie, NY.
Division of Urology, Department of Surgery, University of Tennessee Graduate School of Medicine, Knoxville, TN.
Urology. 2014 Jun;83(6):1326-33. doi: 10.1016/j.urology.2014.02.019. Epub 2014 Apr 13.
To evaluate, posthoc, the relationship between serum total testosterone and response to therapy in a study of tadalafil once daily for erectile dysfunction (ED).
Men were aged ≥18 years, with ≥3-month history of ED and partial prior response to on-demand (PRN) phosphodiesterase type 5 inhibitor (PDE5I) therapy. A 4-week maximum-dose PRN PDE5I run-in was followed by a 4-week nondrug washout period, then randomization to tadalafil 2.5 mg titrated to 5 mg or tadalafil 5 mg (pooled for analyses) or placebo once daily for 12 weeks. Analyses compared endpoint efficacy results between low- (<300 ng/dL) vs normal-testosterone (≥300 ng/dL) level subgroups.
Improvements for tadalafil vs placebo were significant for the International Index of Erectile Function (IIEF) Erectile Function domain, Intercourse Satisfaction domain, Overall Satisfaction domain, and Question 15 (confidence in the ability to get and keep an erection; all P<.001), and for the Sexual Encounter Profile Questions 1-5 (all P≤.011). Analysis of covariance modeling identified significant treatment-by-subgroup interactions for the IIEF-Overall Satisfaction domain and erection confidence question and Sexual Encounter Profile Question 3. Comparing between tadalafil-treated testosterone subgroups, the IIEF-Erectile Function domain scores improved significantly more in men with normal vs low testosterone (P=.022); no other significant differences were identified for either placebo or tadalafil. No significant differences in pre-existing conditions were observed between tadalafil and placebo within the normal- and low-testosterone subgroups.
In men with partial response to a PRN PDE5I, tadalafil 5 mg once daily significantly improved ED and sexual function vs placebo irrespective of testosterone levels.
在一项每日一次他达拉非治疗勃起功能障碍(ED)的研究中,事后评估血清总睾酮与治疗反应的关系。
男性年龄≥18 岁,ED 病史≥3 个月,按需(PRN)磷酸二酯酶 5 抑制剂(PDE5I)治疗有部分反应。进行为期 4 周的最大剂量 PRN PDE5I 导入期后,进行为期 4 周的无药物洗脱期,然后随机分配至每日一次他达拉非 2.5mg 滴定至 5mg 或他达拉非 5mg(合并分析)或安慰剂治疗 12 周。分析比较低睾酮(<300ng/dL)与正常睾酮(≥300ng/dL)水平亚组之间的终点疗效结果。
与安慰剂相比,他达拉非在国际勃起功能指数(IIEF)勃起功能域、性交满意度域、总体满意度域和问题 15(对获得和维持勃起能力的信心;均 P<.001)以及性遭遇概况问卷 1-5(均 P≤.011)方面有显著改善。协方差分析模型确定了 IIEF-总体满意度域和勃起信心问题以及性遭遇概况问卷 3 存在显著的治疗-亚组交互作用。在接受他达拉非治疗的睾酮亚组之间进行比较,IIEF-勃起功能域评分在正常睾酮和低睾酮男性中均有显著改善(P=.022);在安慰剂或他达拉非组中未发现其他显著差异。在正常和低睾酮亚组中,未观察到他达拉非与安慰剂之间的预先存在疾病有显著差异。
在对 PRN PDE5I 有部分反应的男性中,每日一次他达拉非 5mg 显著改善了 ED 和性功能,与睾酮水平无关。