Montorsi F, Verheyden B, Meuleman E, Jünemann K-P, Moncada I, Valiquette L, Casabé A, Pacheco C, Denne J, Knight J, Segal S, Watkins V S
Department of Urology, Università Vita e Salute San Raffaele, Via Olgettina 60, 20312 Milan, Italy.
Eur Urol. 2004 Mar;45(3):339-44; discussion 344-5. doi: 10.1016/j.eururo.2003.11.010.
To assess the long-term safety and tolerability of tadalafil for patients with erectile dysfunction (ED).
This was a multicentre, open-label, 24-month extension trial involving 1173 men with ED. The mean age was 57 (range 23-83) years and 74.8% of patients were taking concomitant medications for comorbid conditions, including diabetes mellitus in 30.5% of men and hypertension in 29.5%. These patients had participated in 1 of 5 previous 8-week or 12-week randomised, double-blind, placebo-controlled tadalafil studies. In the present trial, the starting 10mg dose of tadalafil could be increased to 20mg if the patient could not achieve satisfactory intercourse or reduced to 5mg for an adverse event that was persistent, intolerable and judged by the investigator to be related to tadalafil.
Four hundred ninety-three (42.0%) men completed 24 months of treatment. In addition, a further 234 (19.9%) completed 18 months of treatment due to a sponsor decision to reduce the study duration. The total tadalafil exposure was 1676.0 patient-years. Tadalafil was safe and well tolerated. Headache (15.8%), dyspepsia (11.8%), nasopharyngitis (11.4%), and back pain (8.2%) were the most common treatment-emergent adverse events. The rate of discontinuations due to adverse events for this 18-24-month study was 6.3% and the rate for any individual event was <1%. Serious adverse events occurred in 8.6% of patients. No consistent pattern of serious adverse events assessed as causally associated with tadalafil administration was observed. None of the four deaths that occurred during the study was assessed as tadalafil related. There were no clinically significant laboratory or electrocardiographic findings or changes in vital signs in mean baseline-to-endpoint analysis attributable to tadalafil. Tadalafil administration was not causally associated with drug-induced hepatotoxicity, neutropenia, thrombocytopenia, or renal dysfunction.
Tadalafil at doses of 5, 10, or 20mg taken as needed up to once daily for 18 to 24 months was safe and well tolerated. These findings support the long-term use of tadalafil in the clinical management of erectile dysfunction.
评估他达拉非对勃起功能障碍(ED)患者的长期安全性和耐受性。
这是一项多中心、开放标签、为期24个月的延长期试验,涉及1173例ED男性患者。平均年龄为57岁(范围23 - 83岁),74.8%的患者因合并症正在服用伴随药物,其中30.5%的男性患有糖尿病,29.5%的男性患有高血压。这些患者曾参与过之前5项为期8周或12周的随机、双盲、安慰剂对照的他达拉非研究中的1项。在本试验中,如果患者无法实现满意的性交,他达拉非的起始剂量10mg可增至20mg;如果出现持续、无法耐受且研究者判定与他达拉非相关的不良事件,则剂量可减至5mg。
493例(42.0%)男性完成了24个月的治疗。此外,由于申办方决定缩短研究时长,另有234例(19.9%)完成了18个月的治疗。他达拉非的总暴露量为1676.0患者 - 年。他达拉非安全且耐受性良好。头痛(15.8%)、消化不良(11.8%)、鼻咽炎(11.4%)和背痛(8.2%)是最常见的治疗中出现的不良事件。在这项18 - 24个月的研究中,因不良事件停药的发生率为6.3%,任何单个事件的发生率均<1%。8.6%的患者发生了严重不良事件。未观察到与他达拉非给药有因果关联的严重不良事件的一致模式。研究期间发生的4例死亡事件均未被判定与他达拉非相关。在平均基线至终点分析中,未发现因他达拉非导致的具有临床意义的实验室检查或心电图结果或生命体征变化。他达拉非给药与药物性肝毒性、中性粒细胞减少、血小板减少或肾功能障碍无因果关联。
按需服用他达拉非,剂量为5mg、10mg或20mg,每日一次,持续18至24个月,安全且耐受性良好。这些研究结果支持他达拉非在勃起功能障碍临床治疗中的长期使用。