Amarenco G, Sutory M, Zachoval R, Agarwal M, Del Popolo G, Tretter R, Compion G, De Ridder D
Hôpital Tenon, Service De Neuro-Urologie Et D'Explorations Perineales, Paris, France.
Urological Department of Traumatological Clinic, Traumatological Hospital, School of Medicine, Masaryk University, Brno, Czech Republic.
Neurourol Urodyn. 2017 Feb;36(2):414-421. doi: 10.1002/nau.22945. Epub 2015 Dec 29.
To investigate the effect on urodynamics of 4 weeks treatment with solifenacin succinate in patients with neurogenic detrusor overactivity (NDO) due to multiple sclerosis (MS) or spinal cord injury (SCI).
SONIC was a prospective, multicenter, double-blind, phase 3b/4 study investigating the efficacy and safety of solifenacin 10 mg in patients with NDO due to MS or SCI. Patients (n = 189) were randomized to placebo or active treatment (solifenacin 5 mg, 10 mg or oxybutynin hydrochloride 15 mg) for 4 weeks, after a 2-week, single-blind, placebo run-in period. The primary endpoint was change in maximum cystometric capacity (MCC) from baseline to end of treatment. The primary analysis compared solifenacin 10 mg versus placebo; all other comparisons were considered secondary. Secondary endpoints included changes in urodynamic parameters, patient-reported outcomes, and safety assessments.
In the primary analysis, solifenacin 10 mg significantly improved mean change from baseline MCC versus placebo (P < 0.001) and was associated with improvements in bladder volume at first contraction and at first leak as well as detrusor pressure at first leak. Similar results were obtained for oxybutynin versus placebo. Patient perception of bladder condition significantly improved with solifenacin 10 mg versus placebo (P = 0.041). There was a clear improvement in quality of life (QoL) in the solifenacin arms versus placebo. The overall incidence of adverse events was low.
In patients with NDO due to MS and SCI, 4 weeks of treatment with solifenacin 10 mg improved urodynamic variables and QoL versus placebo and was well tolerated. Neurourol. Urodynam. 36:414-421, 2017. © 2015 Wiley Periodicals, Inc.
研究琥珀酸索利那新治疗4周对因多发性硬化症(MS)或脊髓损伤(SCI)导致神经源性逼尿肌过度活动(NDO)患者尿动力学的影响。
SONIC是一项前瞻性、多中心、双盲、3b/4期研究,旨在调查10毫克索利那新对因MS或SCI导致NDO患者的疗效和安全性。在为期2周的单盲安慰剂导入期后,189例患者被随机分为安慰剂组或活性治疗组(索利那新5毫克、10毫克或盐酸奥昔布宁15毫克),治疗4周。主要终点是从基线到治疗结束时最大膀胱测压容量(MCC)的变化。主要分析比较了10毫克索利那新与安慰剂;所有其他比较均视为次要分析。次要终点包括尿动力学参数变化、患者报告的结局和安全性评估。
在主要分析中,10毫克索利那新与安慰剂相比,从基线MCC的平均变化有显著改善(P < 0.001),并与首次收缩时和首次漏尿时的膀胱容量改善以及首次漏尿时的逼尿肌压力改善相关。奥昔布宁与安慰剂相比也获得了类似结果。与安慰剂相比,10毫克索利那新使患者对膀胱状况的感知有显著改善(P = 0.041)。与安慰剂相比,索利那新组的生活质量(QoL)有明显改善。不良事件的总体发生率较低。
在因MS和SCI导致NDO的患者中,与安慰剂相比,10毫克索利那新治疗4周可改善尿动力学变量和QoL,且耐受性良好。《神经泌尿学与尿动力学》36:414 - 421,2017年。© 2015威利期刊公司