Journal
MOVEMENT DISORDERS
Volume 26, Issue 5, Pages 813-818Publisher
WILEY-BLACKWELL
DOI: 10.1002/mds.23638
Keywords
minimal clinically important change; Parkinson's disease; clinical global impression; treatment; clinical trial
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Funding
- Teva Pharmaceuticals
- Parkinson's Disease Foundation
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Two common primary efficacy outcome measures in Parkinson's disease (PD) are change in Unified Parkinson's Disease Rating Scale (UPDRS) scores in early PD and change in off time in patients with motor fluctuations. Defining the minimal clinically important change (MCIC) in these outcome measures is important to interpret the clinical relevance of changes observed in clinical trials and other situations. We analyzed data from 2 multicenter, placebo-controlled, randomized clinical trials of rasagiline; TEMPO studied 404 early PD subjects, and PRESTO studied 472 levodopa-treated subjects with motor fluctuations. An anchor-based approach using clinical global impression of improvement (CGI-I) was used to determine MCIC for UPDRS scores and daily off time. MCIC was defined as mean change in actively treated subjects rated minimally improved on CGI-I. Receiver operating characteristic (ROC) curves defined optimal cutoffs discriminating between changed and unchanged subjects. MCIC for improvement in total UPDRS score (parts I-III) in early PD was determined to be -3.5 points based on mean scores and -3.0 points based on ROC curves. In addition, we found an MCIC for reduction in off time of 1.0 hours as defined by mean reduction in off time in active treated subjects self-rated as minimally improved on CGI-I minus mean reduction in off time in placebo-treated subjects self-rated as unchanged (1.9-0.9 hours). We hypothesize that many methodological factors can influence determination of the MCIC, and a range of values is likely to emerge from multiple studies. (C) 2011 Movement Disorder Society
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