Ferreira Joaquim J, Rascol Olivier, Stocchi Fabrizio, Antonini Angelo, Moreira Joana, Castilla-Fernández Guillermo, Rocha José-Francisco, Holenz Joerg, Poewe Werner
IMM - Instituto de Medicina Molecular João Lobo Antunes, Faculdade de Medicina, Universidade Lisboa, Lisbon, Portugal.
CNS - Campus Neurológico, Torres Vedras, Portugal.
Eur J Neurol. 2025 Jan;32(1):e16420. doi: 10.1111/ene.16420.
Catechol-O-methyl transferase (COMT) inhibitors are routinely used to manage motor fluctuations in Parkinson's disease (PD). We assessed the effect of opicapone on motor symptom severity in levodopa-treated patients without motor complications.
This was a randomized, double-blind, 24-week, placebo-controlled study of opicapone 50 mg as adjunct to levodopa (NCT04978597). Levodopa-treated patients without motor complications were randomized to 24 weeks of double-blind treatment with adjunct opicapone 50 mg or matching placebo. The primary efficacy endpoint was the mean change from baseline to week 24 in Movement Disorder Society-Unified Parkinson's Disease Rating Scale Part III (MDS-UPDRS-III) total score.
A total of 355 patients were randomized (opicapone 50 mg n = 177, placebo n = 178) and 322 (91%) completed the double-blind period. The adjusted mean [95% CI] change from baseline to week 24 in MDS-UPDRS-III subscore was -6.5 [-7.9, -5.2] in the opicapone group versus -4.3 [-5.7, 3.0] in the placebo group resulting in a significant difference of -2.2 [-3.9, -0.5] favoring opicapone (p = 0.010). There was no difference in the incidence of patients who developed motor complications (5.5% with opicapone vs. 9.8% with placebo) and the incidence of adverse events considered related to study medication was similar between groups (opicapone 10.2% vs. placebo 13.5%).
Treatment with once-daily adjunct opicapone was well tolerated, improved motor severity, and did not induce the development of motor complications. These results support the clinical usefulness of opicapone in the management of PD patients without motor complications.
儿茶酚-O-甲基转移酶(COMT)抑制剂常用于治疗帕金森病(PD)的运动波动。我们评估了奥匹卡朋对左旋多巴治疗且无运动并发症患者运动症状严重程度的影响。
这是一项随机、双盲、为期24周、安慰剂对照的研究,使用50毫克奥匹卡朋作为左旋多巴的辅助治疗(NCT04978597)。将左旋多巴治疗且无运动并发症的患者随机分为两组,进行为期24周的双盲治疗,一组使用50毫克奥匹卡朋作为辅助治疗,另一组使用匹配的安慰剂。主要疗效终点是从基线到第24周运动障碍协会统一帕金森病评定量表第三部分(MDS-UPDRS-III)总分的平均变化。
共有355例患者被随机分组(50毫克奥匹卡朋组n = 177,安慰剂组n = 178),322例(91%)完成了双盲期。从基线到第24周,奥匹卡朋组MDS-UPDRS-III子评分的调整后平均[95%CI]变化为-6.5[-7.9,-5.2],而安慰剂组为-4.3[-5.7,-3.0],奥匹卡朋组显著优于安慰剂组,差值为-2.2[-3.9,-0.5](p = 0.010)。发生运动并发症的患者发生率无差异(奥匹卡朋组为5.5%,安慰剂组为9.8%),且两组中被认为与研究药物相关的不良事件发生率相似(奥匹卡朋组为10.2%,安慰剂组为13.5%)。
每日一次使用奥匹卡朋作为辅助治疗耐受性良好,可改善运动严重程度,且不会诱发运动并发症。这些结果支持奥匹卡朋在治疗无运动并发症的PD患者中的临床实用性。