Hattori Nobutaka, Mochizuki Hideki, Hasegawa Kazuko, Nomoto Masahiro, Uchida Eiji, Terahara Takaaki, Okawa Koji, Fukuta Hiroyuki
Department of Neurology, Juntendo University Faculty of Medicine, Tokyo, Japan.
Department of Neurology, Osaka University Graduate School of Medicine, Osaka, Japan.
Mov Disord. 2020 Sep;35(9):1565-1573. doi: 10.1002/mds.28071. Epub 2020 May 12.
A dopamine agonist patch is an important treatment option for PD.
A randomized, double-blind, parallel-group, placebo-controlled trial was conducted to evaluate superiority of ropinirole hydrochloride patch over placebo and noninferiority to ropinirole hydrochloride extended-release tablet.
PD patients using levodopa received ropinirole patch (up to 64 mg/d), ropinirole tablets (up to 16 mg/d), or placebo once-daily (double-dummy technique). The primary endpoint was the change from baseline in the total score for the UPDRS Part III (on state) at week 16.
The change of the least squares mean (95% confidence interval) in the UPDRS Part III total score was -9.8 (-10.8 to -8.7) with ropinirole patch, -4.3 (-5.8 to -2.8) with placebo, and -10.1 (-11.2 to -9.1) with ropinirole tablet. The difference between the ropinirole patch and placebo groups was -5.4 (-7.3 to -3.6), demonstrating superiority of the patch over placebo. The difference between the ropinirole patch and tablet groups was 0.3 (-1.2 to 1.8). The upper limit of the 95% confidence interval was smaller than the noninferiority limit of 2.5, demonstrating noninferiority of ropinirole patch to ropinirole tablet. In all three groups, most adverse events were mild or moderate and there were no serious safety concerns.
Once-daily ropinirole patch was effective in advanced PD patients, having demonstrated superiority over placebo and noninferiority to ropinirole tablet, without causing serious safety problems. Ropinirole patch can be an alternative option for PD patients. © 2020 International Parkinson and Movement Disorder Society.
多巴胺激动剂贴剂是帕金森病(PD)的一种重要治疗选择。
开展一项随机、双盲、平行组、安慰剂对照试验,以评估盐酸罗匹尼罗贴剂相对于安慰剂的优越性以及相对于盐酸罗匹尼罗缓释片的非劣效性。
正在使用左旋多巴的PD患者接受罗匹尼罗贴剂(最高64mg/天)、罗匹尼罗片(最高16mg/天)或安慰剂,每日一次(采用双模拟技术)。主要终点是第16周时帕金森病统一评分量表(UPDRS)第三部分(状态)总分相对于基线的变化。
罗匹尼罗贴剂组UPDRS第三部分总分的最小二乘均值(95%置信区间)变化为-9.8(-10.8至-8.7),安慰剂组为-4.3(-5.8至-2.8),罗匹尼罗片剂组为-10.1(-11.2至-9.1)。罗匹尼罗贴剂组与安慰剂组之间的差异为-5.4(-7.3至-3.6),表明贴剂优于安慰剂。罗匹尼罗贴剂组与片剂组之间的差异为0.3(-1.2至1.8)。95%置信区间的上限小于非劣效性界值2.5,表明罗匹尼罗贴剂相对于罗匹尼罗片具有非劣效性。在所有三组中,大多数不良事件为轻度或中度,无严重安全性问题。
每日一次的罗匹尼罗贴剂对晚期PD患者有效,已证明其优于安慰剂且相对于罗匹尼罗片具有非劣效性,且未引起严重安全问题。罗匹尼罗贴剂可为PD患者提供另一种治疗选择。©2020国际帕金森病和运动障碍协会。