Department of Minimally Invasive and Robotic Urologic Surgery and Kidney Transplantation, University of Florence, Florence, Italy.
Department of Urology, Sant'Andrea Hospital, University "La Sapienza", Rome, Italy.
Eur Urol Focus. 2021 Mar;7(2):432-439. doi: 10.1016/j.euf.2019.09.015. Epub 2019 Oct 10.
Safety and efficacy of tamsulosin and tadalafil for men with benign prostatic enlargement (BPE) and/or erectile dysfunction (ED) are defined. However, there are only a few pilot studies on combination therapy with these drugs for men with lower urinary tract symptom (LUTS)/BPE and ED. Moreover, preliminary reports are limited to 12 wk, without any information about subsequent therapies.
To evaluate the impact of discontinuation of tamsulosin versus tadalafil 12 wk after combination therapy.
DESIGN, SETTING, AND PARTICIPANTS: Fifty consecutive patients with moderate-to-severe LUTS (International Prostate Symptom Score [IPSS] > 7) and mild-to-severe ED (International Index of Erectile Function-5 [IIEF-5] < 22) were treated with combination therapy (tamsulosin 0.4mg/d plus tadalafil 5mg/d) for 12 wk. After 12 wk, 25 patients discontinued tamsulosin (Group TAD), while 25 patients discontinued tadalafil (Group TAM).
Efficacy variables were IPSS (total, voiding, storage) and IIEF-5. Paired samples t test and analysis of variance were used.
Groups TAD and TAM presented similar features (age, BMI, metabolic profile) including symptoms scores at baseline. Similar and significant improvements in IPSS (total, voiding, and storage) and IIEF-5 were recorded in both groups after 12 wk of combination therapy (all p< 0.001). Total IPSS was similar between the two groups at the end of the trial. However, we found between-group significant differences from baseline to 24 wk and from 12 to 24 wk in storage-IPSS (Group TAD: -3.32 vs Group TAM: -1.24, p= 0.002; Group TAD: +0.24 vs Group TAM: +1.20, p= 0.040, respectively) and in IIEF-5 (Group TAD: +4.64 vs Group TAM: +0.16, p< 0.001; Group TAD: -1.64 vs Group TAM: -4.40, p= 0.003). No significant treatment-related adverse event was recorded in both groups.
After 12 wk of combination therapy, monotherapy with tadalafil for further 12 wk allows to preserve the improvement of storage IPSS and IIEF-5, in addition to total IPSS.
In this report we evaluated the discontinuation of tamsulosin or tadalafil after 12 wk of combination therapy. We found that tadalafil monotherapy, for a further 12 wk, aids in retaining the improvement of storage symptoms and erectile function.
坦索罗辛和他达拉非治疗良性前列腺增生(BPE)和/或勃起功能障碍(ED)男性的安全性和疗效已经确定。然而,仅有少数关于这些药物联合治疗下尿路症状(LUTS)/BPE 和 ED 男性的试点研究。此外,初步报告仅限于 12 周,没有任何关于后续治疗的信息。
评估联合治疗 12 周后停用坦索罗辛与他达拉非的影响。
设计、地点和参与者:50 例中重度 LUTS(国际前列腺症状评分 [IPSS] > 7)和轻至重度 ED(国际勃起功能指数-5 [IIEF-5] < 22)的连续患者接受联合治疗(坦索罗辛 0.4mg/d 加他达拉非 5mg/d)12 周。12 周后,25 例患者停用坦索罗辛(TAD 组),25 例患者停用他达拉非(TAM 组)。
疗效变量为 IPSS(总分、排尿、储存)和 IIEF-5。采用配对样本 t 检验和方差分析。
TAD 组和 TAM 组的特征(年龄、BMI、代谢谱)相似,包括基线时的症状评分。两组在联合治疗 12 周后均记录到 IPSS(总分、排尿和储存)和 IIEF-5 的显著改善(均 p<0.001)。在试验结束时,两组的总 IPSS 相似。然而,我们发现从基线到 24 周以及从 12 周到 24 周,储存 IPSS(TAD 组:-3.32 对 TAM 组:-1.24,p=0.002;TAD 组:+0.24 对 TAM 组:+1.20,p=0.040)和 IIEF-5(TAD 组:+4.64 对 TAM 组:+0.16,p<0.001;TAD 组:-1.64 对 TAM 组:-4.40,p=0.003)存在组间显著差异。两组均未记录到与治疗相关的不良事件。
联合治疗 12 周后,再用他达拉非治疗 12 周可保持储存 IPSS 和 IIEF-5 的改善,此外还可保持总 IPSS 的改善。
在本报告中,我们评估了联合治疗 12 周后停用坦索罗辛或他达拉非的情况。我们发现,他达拉非单药治疗 12 周,有助于保持储存症状和勃起功能的改善。