期刊
NEW ENGLAND JOURNAL OF MEDICINE
卷 361, 期 13, 页码 1268-1278出版社
MASSACHUSETTS MEDICAL SOC
DOI: 10.1056/NEJMoa0809335
关键词
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资金
- Eutherapie
- Novartis
- Boehringer Ingelheim
- Pierre Fabre
- GlaxoSmithKline
- Lund beck
- Advanced Neuromodulation Systems
- Ceregene
- Medtronic Neurological
- Kyowa
- Schwarz Biosciences
- SkyePharm
- Chelsea Therapeutics
- Solvay
- Neurogen
- Eisai
- AstraZeneca
Background A therapy that slows disease progression is the major unmet need in Parkinson's disease. Methods In this double-blind trial, we examined the possibility that rasagiline has disease-modifying effects in Parkinson's disease. A total of 1176 subjects with untreated Parkinson's disease were randomly assigned to receive rasagiline (at a dose of either 1 mg or 2 mg per day) for 72 weeks (the early-start group) or placebo for 36 weeks followed by rasagiline (at a dose of either 1 mg or 2 mg per day) for 36 weeks (the delayed-start group). To determine a positive result with either dose, the early-start treatment group had to meet each of three hierarchical end points of the primary analysis based on the Unified Parkinson's Disease Rating Scale (UPDRS, a 176-point scale, with higher numbers indicating more severe disease): superiority to placebo in the rate of change in the UPDRS score between weeks 12 and 36, superiority to delayed-start treatment in the change in the score between baseline and week 72, and noninferiority to delayed-start treatment in the rate of change in the score between weeks 48 and 72. Results Early-start treatment with rasagiline at a dose of 1 mg per day met all end points in the primary analysis: a smaller mean (+/- SE) increase ( rate of worsening) in the UPDRS score between weeks 12 and 36 (0.09 +/- 0.02 points per week in the early-start group vs. 0.14 +/- 0.01 points per week in the placebo group, P=0.01), less worsening in the score between baseline and week 72 (2.82 +/- 0.53 points in the early-start group vs. 4.52 +/- 0.56 points in the delayed-start group, P=0.02), and noninferiority between the two groups with respect to the rate of change in the UPDRS score between weeks 48 and 72 (0.085 +/- 0.02 points per week in the early-start group vs. 0.085 +/- 0.02 points per week in the delayed-start group, P<0.001). All three end points were not met with rasagiline at a dose of 2 mg per day, since the change in the UPDRS score between baseline and week 72 was not significantly different in the two groups (3.47 +/- 0.50 points in the early-start group and 3.11 +/- 0.50 points in the delayed- start group, P=0.60). Conclusions Early treatment with rasagiline at a dose of 1 mg per day provided benefits that were consistent with a possible disease-modifying effect, but early treatment with rasagiline at a dose of 2 mg per day did not. Because the two doses were associated with different outcomes, the study results must be interpreted with caution. (ClinicalTrials. gov number, NCT00256204.)
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