Kelleher Con J, Cardozo Linda, Chapple Christopher R, Haab Francois, Ridder Arwin M
Guy's and St. Thomas' Hospital, London, UK.
BJU Int. 2005 Jan;95(1):81-5. doi: 10.1111/j.1464-410X.2004.05255.x.
To assess the effect of solifenacin succinate treatment on quality of life (QoL) measured in clinical trials in patients with overactive bladder (OAB).
QoL data using the King's Health Questionnaire (KHQ) were analysed from two phase-3, 12-week studies (1984 patients) and a long-term extension of these studies (1637 patients) where patients received solifenacin for up to an additional 40 weeks (i.e. a 52-week exposure to solifenacin). The 12-week studies were multinational, multicentre, randomized, double-blind, and placebo-controlled. The 10 domains from the KHQ evaluated were general health perception, incontinence impact, role limitations, physical limitations, social limitations, personal relationships, emotions, sleep/energy, severity measures, and symptom severity. Changes from baseline to endpoint in QoL variables were assessed by analysis of variance, and from pooled outcomes of the 12-week studies by analysis of covariance. Descriptive statistics were used to evaluate data in the extension study.
In the two 12-week studies (1033 and 857 patients), those receiving once-daily solifenacin had statistically significantly better QoL than those on placebo. Changes in the KHQ were statistically significantly (P < 0.05) different from placebo for both solifenacin 5 and 10 mg once daily on five of the 10 KHQ domains in each of the studies. Pooled data from the two 12-week studies showed statistically significant (P < 0.05) differences from placebo for both solifenacin doses in nine of the 10 domains. Improvements in QoL scores for solifenacin were 35-48% in nine of the 10 domains for the 1347 patients providing QoL data in the extension study. About two-thirds of this overall improvement occurred during the original 12-week study, with an additional third reported during the extension, with an improvement in QoL over time in patients treated with solifenacin.
Results from the KHQ in study participants in the two double-blind studies showed that solifenacin significantly improved the QoL in patients with OAB symptoms after 12 weeks of treatment, with further improvements during long-term administration up to 1 year. Clinical trial outcomes show a favourable balance of efficacy and tolerability with solifenacin; the present report further supports this efficacy and tolerability by providing evidence for both short- and long-term improvements in QoL.
评估琥珀酸索利那新治疗对膀胱过度活动症(OAB)患者在临床试验中所测量的生活质量(QoL)的影响。
使用国王健康问卷(KHQ)的生活质量数据来自两项为期12周的3期研究(1984例患者)以及这些研究的长期扩展研究(1637例患者),其中患者接受索利那新治疗长达40周(即接受索利那新治疗52周)。这两项为期12周的研究为多中心、多国、随机、双盲且安慰剂对照研究。KHQ评估的10个领域包括总体健康感知、尿失禁影响、角色限制、身体限制、社交限制、人际关系、情绪、睡眠/精力、严重程度测量以及症状严重程度。生活质量变量从基线到终点的变化通过方差分析进行评估,12周研究的汇总结果通过协方差分析进行评估。描述性统计用于评估扩展研究中的数据。
在两项为期12周的研究(分别为1033例和857例患者)中,每日一次服用索利那新的患者在生活质量方面在统计学上显著优于服用安慰剂的患者。在每项研究的10个KHQ领域中的5个领域,索利那新5毫克和10毫克每日一次组在KHQ方面的变化与安慰剂相比在统计学上有显著差异(P < 0.05)。两项为期12周研究的汇总数据显示在10个领域中的9个领域,两种索利那新剂量与安慰剂相比在统计学上有显著差异(P < 0.05)。在扩展研究中提供生活质量数据并接受索利那新治疗的1347例患者中,在10个领域中的9个领域,索利那新的生活质量评分改善幅度为35%至48%。总体改善的约三分之二发生在最初的12周研究期间,另外三分之一在扩展期间报告,接受索利那新治疗的患者生活质量随时间有所改善。
两项双盲研究中研究参与者的KHQ结果表明,索利那新在治疗12周后显著改善了OAB症状患者的生活质量,在长达1年的长期给药期间进一步改善。临床试验结果显示索利那新在疗效和耐受性方面具有良好的平衡;本报告通过提供短期和长期生活质量改善的证据进一步支持了这种疗效和耐受性。