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左旋多巴/多巴脱羧酶抑制剂复方制剂与恩他卡朋治疗帕金森病患者的五年疗效和安全性

Five-year efficacy and safety of levodopa/DDCI and entacapone in patients with Parkinson's disease.

作者信息

Brooks David J, Leinonen Mika, Kuoppamäki Mikko, Nissinen Helena

机构信息

Division of Neuroscience, Faculty of Medicine, Imperial College, Hammersmith Hospital, London, UK.

出版信息

J Neural Transm (Vienna). 2008 Jun;115(6):843-9. doi: 10.1007/s00702-008-0025-8. Epub 2008 Feb 8.

Abstract

This was a retrospective pooled analysis of data from four comparably designed, double-blind, placebo-controlled, Phase III studies and their long-term open-label extensions. Patients on levodopa and a dopa decarboxylase inhibitor (DDCI) were randomized to entacapone or to placebo in the 6-month, double-blind phase, with all patients subsequently receiving entacapone in the extension phase. UPDRS III motor scores improved by -2.1 points during the first 6 months of levodopa/DDCI and entacapone therapy, and remained below baseline for up to 2 years. Increased daily 'ON' time, together with response duration to a single morning dose of levodopa and clinical global evaluation, also supported the long-term efficacy of levodopa/DDCI and entacapone. The mean daily dose of levodopa did not increase over the 5-year follow-up period. Long-term therapy with levodopa/DDCI and entacapone was well-tolerated.

摘要

这是一项对四项设计相似的双盲、安慰剂对照III期研究及其长期开放标签扩展研究的数据进行的回顾性汇总分析。在为期6个月的双盲阶段,服用左旋多巴和多巴脱羧酶抑制剂(DDCI)的患者被随机分为接受恩他卡朋或安慰剂治疗,所有患者随后在扩展阶段均接受恩他卡朋治疗。在左旋多巴/DDCI和恩他卡朋治疗的前6个月,统一帕金森病评定量表(UPDRS)III运动评分改善了-2.1分,并且在长达2年的时间里一直低于基线水平。每日“开”期时间增加,以及对单次晨起剂量左旋多巴的反应持续时间和临床整体评估,也支持了左旋多巴/DDCI和恩他卡朋的长期疗效。在5年的随访期内,左旋多巴的平均每日剂量没有增加。左旋多巴/DDCI和恩他卡朋的长期治疗耐受性良好。

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