Bump Richard C, Voss Simon, Beardsworth Anthony, Manning Martina, Zhao Yan D, Chen Wei
Lilly Research Laboratories, Indianapolis, IN 46285, USA.
BJU Int. 2008 Jul;102(2):214-8. doi: 10.1111/j.1464-410X.2008.07577.x. Epub 2008 Jul 1.
To assess the maintenance of efficacy of duloxetine beyond 3 months, using data from several long-term, open-label studies, as the efficacy of duloxetine 40-mg twice daily for treating women with stress urinary incontinence (SUI) for up to 3 months has been established in several randomized, placebo-controlled clinical trials.
Data from 1424 patients (Cohort A) enrolled in three 12-week, placebo-controlled clinical trials and their uncontrolled, open-label extensions, and in one uncontrolled, open-label study, were used to assess long-term continuation rates and continued efficacy based on responses to the validated Patient Global Impression of Improvement (PGI-I) scale for up to 30 months. Data from another 2758 patients (Cohort B) enrolled in an additional placebo-controlled study and its open-label extension were used to assess PGI-I ratings, reductions in incontinence episode frequency (IEF) recorded on urinary diaries, and the relationship between PGI-I ratings and reductions in IEF for up to 72 weeks.
In Cohort A, the duloxetine continuation rate at 1 year was 42.5%. At 12, 24 and 30 months, most (83%, 83% and 88%, respectively) patients in Cohort A who continued treatment rated their incontinence in one of the three 'better since starting treatment' PGI-I categories. Both the median IEF reductions (50-77%) and the PGI-I 'better' ratings (70-88% of patients) remained fairly consistent over 72 weeks in Cohort B. Finally, IEF reductions increased with increasing PGI-I ratings (approximately 46% for 'a little better', 75% for 'much better' and 95% for 'very much better') over the first year of treatment.
The benefits of duloxetine were maintained in patients who continued treatment for up to 30 months. However, these favourable results need to be interpreted cautiously, as many patients discontinued treatment and those with better responses are more likely to continue taking medication.
利用多项长期开放标签研究的数据,评估度洛西汀治疗超过3个月的疗效维持情况,因为在多项随机、安慰剂对照临床试验中已证实,每日两次服用40毫克度洛西汀治疗压力性尿失禁(SUI)女性长达3个月的疗效。
来自1424例患者(队列A)的数据,这些患者参加了三项为期12周的安慰剂对照临床试验及其非对照、开放标签延长期试验,以及一项非对照、开放标签研究,用于评估长达30个月的长期持续率和基于有效患者总体改善印象(PGI-I)量表反应的持续疗效。来自另外2758例患者(队列B)的数据,这些患者参加了另一项安慰剂对照研究及其开放标签延长期试验,用于评估PGI-I评分、尿日记记录的尿失禁发作频率(IEF)降低情况,以及长达72周的PGI-I评分与IEF降低之间的关系。
在队列A中,1年时度洛西汀的持续率为42.5%。在12个月、24个月和30个月时,队列A中继续治疗的大多数患者(分别为83%、83%和88%)将其尿失禁评定为PGI-I三个“自开始治疗后病情好转”类别中的一种。在队列B中,中位数IEF降低(50%-77%)和PGI-I“好转”评分(70%-88%的患者)在72周内保持相当一致。最后,在治疗的第一年,IEF降低随着PGI-I评分的增加而增加(“稍好转”约为46%,“明显好转”为75%,“非常明显好转”为95%)。
继续治疗长达30个月的患者维持了度洛西汀的益处。然而,这些有利结果需要谨慎解读,因为许多患者停止了治疗,且反应较好的患者更有可能继续服药。