Abstract

Background: Levodopa-carbidopa intestinal gel (LCIG) is a long-term therapy for motor fluctuations in patients with advanced Parkinson's disease (PD). The aim of this analysis was to identify the baseline characteristics that predict “Off” time reduction in advanced PD patients treated with LCIG under routine clinical care in the GLORIA registry.Methods: Patients were followed under routine care for 24 months (M) with delivery of LCIG via percutaneous gastrojejunostomy. Analysis of covariance (ANCOVA) and logistic regression were performed to identify baseline characteristics that predict “Off” time reduction.Results: Compared to baseline, 86% (n/N = 131/152; mean ± SD baseline “Off” time: 3.4 ± 2.2 h) of M24 completers had ≥ 1 h reduction in “Off” time and 64% (n/N = 97/152; mean ± SD baseline “Off” time: 7.6 ± 2.9 h) had ≥ 3 h “Off” time reduction at M24. Most baseline characteristics were similar across responder subgroups; however, patients with ≥ 3 h “Off” time improvement had more “Off” time and less time with dyskinesia at baseline compared to patients with <3 h “Off” time reduction. Despite having less improvement in absolute “Off” h at M24, patients with <3 h “Off” time reduction experienced a 33% median reduction in “Off” time and a 44% median reduction in dyskinesia duration at M24, which was similar to the dyskinesia improvement observed among patients with ≥ 3 h “Off” time improvement (50% median reduction). Baseline “Off” time was both the best predictor of and the only significant factor associated with “Off” time improvement (P <0.0001).Conclusions: LCIG treatment led to clinically meaningful improvements in “Off” time in 86% of advanced PD patients and those with greater “Off” time are likely to experience the largest absolute reduction in hours “Off.”

Highlights

  • Stages of Parkinson’s disease (PD) are well-controlled with standard oral levodopa therapy; long-term oral treatment is associated with the development of disabling motor and non-motor fluctuations

  • One long-term treatment option for advanced PD patients is levodopa-carbidopa intestinal gel (LCIG, carbidopa-levodopa enteral suspension in the United States [CLES]) that is continuously delivered to the upper intestine via percutaneous gastrojejunostomy (PEGJ) and a portable infusion pump

  • A recent publication that evaluated LCIGtreated patients from a phase 3 clinical trial reported that a patient’s baseline “Off ” time was a strong predictor of whether or not a patient experienced clinically meaning improvements in “Off ” time over the course of treatment [10]. These analyses were performed in clinical trials and it is unknown if this observation applies to the use of Levodopa-carbidopa intestinal gel (LCIG) in routine clinical practice

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Summary

Introduction

Stages of Parkinson’s disease (PD) are well-controlled with standard oral levodopa therapy; long-term oral treatment is associated with the development of disabling motor and non-motor fluctuations. A recent publication that evaluated LCIGtreated patients from a phase 3 clinical trial reported that a patient’s baseline “Off ” time was a strong predictor of whether or not a patient experienced clinically meaning improvements in “Off ” time over the course of treatment [10] These analyses were performed in clinical trials and it is unknown if this observation applies to the use of LCIG in routine clinical practice. Levodopa-carbidopa intestinal gel (LCIG) is a long-term therapy for motor fluctuations in patients with advanced Parkinson’s disease (PD). The aim of this analysis was to identify the baseline characteristics that predict “Off” time reduction in advanced PD patients treated with LCIG under routine clinical care in the GLORIA registry

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