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左旋多巴-卡比多巴肠凝胶治疗晚期帕金森病的长期安全性和疗效。

Long-term safety and efficacy of levodopa-carbidopa intestinal gel in advanced Parkinson's disease.

机构信息

Center for Neurological Restoration, Cleveland Clinic, Cleveland, Ohio, USA.

University of Vermont Larner College of Medicine, Burlington, Vermont, USA.

出版信息

Mov Disord. 2018 Jul;33(6):928-936. doi: 10.1002/mds.27338. Epub 2018 Mar 23.

Abstract

BACKGROUND

Levodopa-carbidopa intestinal gel (designated as carbidopa-levodopa enteral suspension in the United States) provides stable plasma levodopa concentrations and reduces motor fluctuations in advanced Parkinson's disease patients through continuous delivery of levodopa via percutaneous endoscopic gastrojejunostomy. We report long-term safety and efficacy outcomes from an open-label phase 3 treatment program.

METHODS

PD patients (n = 262) who completed a 12-week double-blind study and its 52-week open-label extension or a separate 54-week open-label study were enrolled in this ongoing phase 3 open-label, multinational study (NCT00660673). Safety and efficacy assessments were collected every 6 months.

RESULTS

Mean total duration of exposure to levodopa-carbidopa intestinal gel was 4.1 years (range, 1.2 to 6.9 years). The overall discontinuation rate was 34% (average annual discontinuation rate, 10%). Although most patients (94%) reported an adverse event, the rate of adverse events decreased over time; 53% experienced a serious adverse event. Of patients in this extension study, 54% required jejunal tube replacement during the study, and 37% required percutaneous endoscopic gastrostomy tube replacement. Most patients were on levodopa monotherapy. Patients maintained reductions in "off" time and increases in mean "on" time without dyskinesia from initial levodopa-carbidopa intestinal gel infusion to he study end point (P < 0.001; n = 81). Activities of daily living and quality-of-life assessments demonstrated significant improvements that persisted through the study.

CONCLUSIONS

This long-term study demonstrates sustained and clinically meaningful benefits from levodopa-carbidopa intestinal gel in advanced PD patients. Although adverse event rates decreased over time, vigilance is required for device-related complications and adverse events. © 2018 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society.

摘要

背景

左旋多巴-卡比多巴肠凝胶(在美国被指定为卡比多巴-左旋多巴肠内混悬液)通过经皮内镜胃空肠造口术持续输送左旋多巴,为晚期帕金森病患者提供稳定的血浆左旋多巴浓度并减少运动波动。我们报告了一项开放标签的 3 期治疗计划的长期安全性和疗效结果。

方法

完成 12 周双盲研究及其 52 周开放标签扩展或单独 54 周开放标签研究的 PD 患者(n = 262)被纳入这项正在进行的 3 期开放标签、多国研究(NCT00660673)。每 6 个月收集安全性和疗效评估。

结果

平均暴露于左旋多巴-卡比多巴肠凝胶的总持续时间为 4.1 年(范围 1.2 至 6.9 年)。总的停药率为 34%(平均年停药率为 10%)。尽管大多数患者(94%)报告了不良事件,但不良事件的发生率随时间降低;53%发生严重不良事件。在这项扩展研究中,54%的患者在研究期间需要更换空肠管,37%的患者需要更换经皮内镜胃造口管。大多数患者接受左旋多巴单药治疗。患者维持从初始左旋多巴-卡比多巴肠凝胶输注到研究终点时的“关期”减少和“开期”时间平均增加而无运动障碍(P < 0.001;n = 81)。日常生活活动和生活质量评估显示出显著的改善,并持续到研究结束。

结论

这项长期研究表明,在晚期 PD 患者中,左旋多巴-卡比多巴肠凝胶具有持续和有临床意义的益处。尽管不良事件发生率随时间降低,但需要警惕与器械相关的并发症和不良事件。© 2018 作者。运动障碍由 Wiley Periodicals, Inc. 代表国际帕金森病和运动障碍协会出版。

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