Hauser Robert A, Abler Victor, Eyal Eli, Eliaz Rom E
a Parkinson's Disease and Movement Disorders Center , University of South Florida, National Parkinson Foundation Center of Excellence , Tampa , FL , USA.
b Teva Pharmaceuticals , Frazer , PA , USA , and.
Int J Neurosci. 2016 Oct;126(10):942-6. doi: 10.3109/00207454.2016.1154552. Epub 2016 Mar 18.
To evaluate the efficacy of rasagiline versus placebo in a pooled population of patients with early Parkinson's disease (PD).
TEMPO and ADAGIO were Phase III studies that evaluated the symptomatic efficacy of rasagiline versus placebo in patients with early PD. This meta-analysis included Unified Parkinson's Disease Rating Scale (UPDRS) observations from weeks 12, 24 and 36 in ADAGIO and from weeks 14 and 26 in TEMPO; TEMPO visits were recoded to weeks 12 and 24, respectively. The present analysis includes all patients who received rasagiline 1 mg/day, 2 mg/day or placebo, and had ≥1 post-baseline observations and a subgroup of patients whose baseline UPDRS Total scores were ≥27 (Upper Quartile population). Change from baseline in UPDRS scores were evaluated using mixed models repeated measures analyses.
Of the 1578 patients randomized to the two studies, 1546 patients met criteria for inclusion in the meta-analysis. Effects on UPDRS Total, motor and activities of daily living scores were significantly better for both doses of rasagiline compared with placebo at all time periods. The Upper Quartile population included 402 patients with a UPDRS Total score ≥27 at baseline. These patients generally demonstrated a larger magnitude of treatment effect than was seen in the full population.
This meta-analysis confirms the efficacy of rasagiline monotherapy over 36 weeks. Although TEMPO and ADAGIO are considered studies of "very early" PD, both contained a sizeable pool of patients with more severe disease. In addition, the meta-analysis showed a larger magnitude of effect in patients with more severe baseline disease.
评估雷沙吉兰与安慰剂在早期帕金森病(PD)合并人群中的疗效。
TEMPO和ADAGIO是评估雷沙吉兰与安慰剂对早期PD患者症状疗效的III期研究。这项荟萃分析纳入了ADAGIO研究中第12、24和36周以及TEMPO研究中第14和26周的统一帕金森病评定量表(UPDRS)观察结果;TEMPO研究的访视时间分别重新编码为第12周和第24周。本分析包括所有接受1mg/天、2mg/天雷沙吉兰或安慰剂治疗且基线后有≥1次观察结果的患者,以及基线UPDRS总分≥27的患者亚组(上四分位数人群)。使用混合模型重复测量分析评估UPDRS评分相对于基线的变化。
在随机分配到这两项研究的1578例患者中,1546例患者符合纳入荟萃分析的标准。在所有时间段,两种剂量的雷沙吉兰对UPDRS总分、运动及日常生活评分的影响均显著优于安慰剂。上四分位数人群包括402例基线时UPDRS总分≥27的患者。这些患者总体上表现出比全部人群更大的治疗效果。
这项荟萃分析证实了雷沙吉兰单药治疗36周的疗效。尽管TEMPO和ADAGIO被视为“极早期”PD的研究,但两者都包含了相当数量病情较重的患者。此外,荟萃分析显示,基线疾病较重的患者治疗效果更大。