Schimrigk Sebastian, Marziniak Martin, Neubauer Christine, Kugler Eva Maria, Werner Gudrun, Abramov-Sommariva Dimitri
Märkische Kliniken GmbH, Klinikum Lüdenscheid, Klinik für Neurologie, Lüdenscheid, Germany.
Kbo-Isar-Amper-Klinikum München-Ost, Klinik für Neurologie, Haar, Germany.
Eur Neurol. 2017;78(5-6):320-329. doi: 10.1159/000481089. Epub 2017 Oct 26.
Treatment of neuropathic pain (NP) symptoms associated with multiple sclerosis (MS) is frequently insufficient. Yet, cannabis is still rarely offered for treatment of pain. This clinical trial aimed at showing the positive benefit-risk ratio of dronabinol. Two hundred forty MS patients with central NP entered a 16-weeks placebo-controlled phase-III study followed by a 32-weeks open-label period. One hundred patients continued therapy for overall up to 119 weeks. Primary endpoint was change of pain intensity on the 11-point Numerical Rating Scale over a 16-weeks treatment period. Safety was assessed on the basis of adverse reactions (ARs), signs of dependency and abuse. Pain intensity during 16-weeks dronabinol and placebo treatment was reduced by 1.92 and 1.81 points without significant difference in between (p = 0.676). Although the proportion of patients with ARs was higher under dronabinol compared to placebo (50.0 vs. 25.9%), it decreased during long-term use of dronabinol (26%). No signs of drug abuse and only one possible case of dependency occurred. The trial results demonstrate that dronabinol is a safe long-term treatment option.
与多发性硬化症(MS)相关的神经性疼痛(NP)症状的治疗常常并不充分。然而,大麻仍很少被用于疼痛治疗。这项临床试验旨在证明屈大麻酚的积极效益风险比。240名患有中枢性NP的MS患者进入了一项为期16周的安慰剂对照III期研究,随后是为期32周的开放标签期。100名患者持续治疗长达119周。主要终点是在16周治疗期内11点数字评分量表上的疼痛强度变化。根据不良反应(ARs)、依赖和滥用迹象评估安全性。屈大麻酚和安慰剂治疗16周期间的疼痛强度分别降低了1.92和1.81分,两者之间无显著差异(p = 0.676)。尽管与安慰剂相比,屈大麻酚治疗下出现ARs的患者比例更高(50.0%对25.9%),但在屈大麻酚长期使用期间这一比例下降了(26%)。未出现药物滥用迹象,仅发生了1例可能的依赖情况。试验结果表明,屈大麻酚是一种安全的长期治疗选择。