Department of Pharmacology, National University of Singapore, Clinical Research Centre, Singapore, Singapore.
Stroke. 2013 Aug;44(8):2093-100. doi: 10.1161/STROKEAHA.113.002055. Epub 2013 Jun 18.
Previous clinical studies suggested benefit for poststroke recovery when MLC601 was administered between 2 weeks and 6 months of stroke onset. The Chinese Medicine Neuroaid Efficacy on Stroke recovery (CHIMES) study tested the hypothesis that MLC601 is superior to placebo in acute, moderately severe ischemic stroke within a 72-hour time window.
This multicenter, double-blind, placebo-controlled trial randomized 1100 patients with a National Institutes of Health Stroke Scale score 6 to 14, within 72 hours of onset, to trial medications for 3 months. The primary outcome was a shift in the modified Rankin Scale. Secondary outcomes were modified Rankin Scale dichotomy, National Institutes of Health Stroke Scale improvement, difference in National Institutes of Health Stroke Scale total and motor scores, Barthel index, and mini-mental state examination. Planned subgroup analyses were performed according to age, sex, time to first dose, baseline National Institutes of Health Stroke Scale, presence of cortical signs, and antiplatelet use.
The modified Rankin Scale shift analysis-adjusted odds ratio was 1.09 (95% confidence interval, 0.86-1.32). Statistical difference was not detected between the treatment groups for any of the secondary outcomes. Subgroup analyses showed no statistical heterogeneity for the primary outcome; however, a trend toward benefit in the subgroup receiving treatment beyond 48 hours from stroke onset was noted. Serious and nonserious adverse events rates were similar between the 2 groups.
MLC601 is statistically no better than placebo in improving outcomes at 3 months when used among patients with acute ischemic stroke of intermediate severity. Longer treatment duration and follow-up of participants with treatment initiated after 48 hours may be considered in future studies.
URL: http://www.clinicaltrials.gov. Unique identifier: NCT00554723.
既往临床研究提示,MLC601 治疗时间窗为卒中发病后 2 周至 6 个月时,对卒中后恢复有益。中药神经修复剂(Neuroaid)治疗卒中恢复的疗效研究(CHIMES)旨在检验 MLC601 在 72 小时时间窗内治疗急性、中度严重缺血性卒中的疗效是否优于安慰剂。
本多中心、双盲、安慰剂对照临床试验纳入发病 72 小时内、NIHSS 评分 6 至 14 分的 1100 例患者,随机分组接受试验药物治疗 3 个月。主要结局为改良 Rankin 量表(mRS)评分变化。次要结局为 mRS 评分二分位数、NIHSS 评分改善、NIHSS 总分及运动评分差值、Barthel 指数和简易精神状态检查(MMSE)。根据年龄、性别、首次给药时间、基线 NIHSS 评分、皮质体征和抗血小板药物使用情况进行计划亚组分析。
mRS 评分变化分析校正比值比为 1.09(95%置信区间:0.86~1.32)。治疗组间在任何次要结局上均未发现统计学差异。主要结局的亚组分析未见统计学异质性;然而,发病后 48 小时以上开始治疗的亚组存在获益趋势。两组严重和非严重不良事件发生率相似。
在治疗中度严重急性缺血性卒中患者时,与安慰剂相比,MLC601 在 3 个月时改善结局的效果无统计学差异。在未来研究中,可考虑延长治疗时间,并对发病后 48 小时后开始治疗的患者进行更长时间的随访。