Vokurka Petr, Barron Andrew, Sumaria Sheetal, Stockford Lindsey, Jarman Paul, Bhatia Kailash, Farmer Simon, Saifee Tabish, Warner Tom, Weil Rimona, Gandhi Sonia, Limousin Patricia, Korlipara Prasad, Foltynie Tom
Department of Clinical & Movement Neurosciences University College London Institute of Neurology London UK.
The National Hospital for Neurology and Neurosurgery, Queen Square London UK.
Mov Disord Clin Pract. 2020 Oct 21;7(8):955-960. doi: 10.1002/mdc3.13094. eCollection 2020 Nov.
Opicapone, a recently introduced catechol-o-methyl transferase (COMT) inhibitor has the advantage of being administered once daily, and has pharmacokinetic data to indicate it offers a greater degree of COMT inhibition than entacapone. Although trial data indicate it is non-inferior to entacapone, there are no data to indicate whether it offers any clinical advantages.
In this audit, we present data from 57 individuals prescribed opicapone at the National Hospital for Neurology and Neurosurgery, Queen Square who had either not tolerated or reported insufficient benefit following previous prescription of entacapone.
A total of 20 of 57 patients switched directly from entacapone to opicapone ("entacapone switchers") whereas 37 of 57 patients had previously discontinued entacapone because of lack of benefit or adverse events ("entacapone failures"). A total of 21 of 57 (37%) patients stopped opicapone prior to 6 months. A total of 7 of 20 (35%) "entacapone switchers" experienced adverse events with opicapone of which 5 stopped the drug prior to the 6 month evaluation of efficacy. A total of 23 of 37 (62%) "entacapone failures" reported adverse events of which 16 stopped the drug. Among 36 of 57 (63%) patients who continued to use opicapone at 6 months, there was an improvement in OFF time of ~2 hours per day as measured by interview.
We conclude that opicapone can be an effective additional treatment for wearing off in Parkinson's disease (PD) in a subgroup of patients. The use of opicapone in our cohort with prior entacapone exposure, however, was associated with higher rates of adverse effects and treatment discontinuation than reported in published trial data of COMT inhibitor naïve patients.
奥匹卡朋是一种最近推出的儿茶酚-O-甲基转移酶(COMT)抑制剂,具有每日给药一次的优势,其药代动力学数据表明,与恩他卡朋相比,它对COMT的抑制程度更高。尽管试验数据表明它不劣于恩他卡朋,但尚无数据表明它是否具有任何临床优势。
在本次审计中,我们提供了来自伦敦女王广场国立神经病学与神经外科医院57例服用奥匹卡朋患者的数据,这些患者要么对恩他卡朋不耐受,要么在先前使用恩他卡朋治疗后疗效不佳。
57例患者中,共有20例直接从恩他卡朋换用奥匹卡朋(“恩他卡朋换药者”),而57例患者中有37例此前因疗效不佳或不良事件而停用恩他卡朋(“恩他卡朋治疗失败者”)。57例患者中共有21例(37%)在6个月前停用奥匹卡朋。20例“恩他卡朋换药者”中有7例(35%)出现奥匹卡朋相关不良事件,其中5例在6个月疗效评估前停药。37例“恩他卡朋治疗失败者”中有23例(62%)报告了不良事件,其中16例停药。在6个月时继续使用奥匹卡朋的57例患者中的36例(63%)中,通过访谈测量,每日“关”期时间改善约2小时。
我们得出结论,奥匹卡朋可以作为帕金森病(PD)一部分患者症状波动的有效附加治疗方法。然而,在我们这个先前使用过恩他卡朋的队列中,奥匹卡朋的使用与更高的不良反应发生率和停药率相关,高于未使用过COMT抑制剂的患者的已发表试验数据中所报告的情况。