Brooks David J, Leinonen Mika, Kuoppamäki Mikko, Nissinen Helena
Division of Neuroscience, Faculty of Medicine, Imperial College, Hammersmith Hospital, London, UK.
J Neural Transm (Vienna). 2008 Jun;115(6):843-9. doi: 10.1007/s00702-008-0025-8. Epub 2008 Feb 8.
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.
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。