Hauser Robert A, Hewitt L Arthur, Isaacson Stuart
University of South Florida, Tampa, FL, USA.
Chelsea Therapeutics, Inc., Charlotte, NC, USA.
J Parkinsons Dis. 2014;4(1):57-65. doi: 10.3233/JPD-130259.
Neurogenic orthostatic hypotension (nOH) is common in Parkinson's disease (PD), and represents a failure to generate norepinephrine responses appropriate for postural change. Droxidopa (L-threo-3,4-dihydroxyphenylserine) is an oral norepinephrine prodrug.
Interim analyses of the initial patients enrolled in a multicenter, randomized, double-blind, placebo-controlled phase 3 trial of droxidopa for nOH in PD (ClinicalTrials.gov Identifier: NCT01176240).
PD patients with documented nOH underwent ≤ 2 weeks of double-blind droxidopa or placebo dosage optimization followed by 8 weeks of maintenance treatment (100-600 mg t.i.d.). The primary efficacy measure was change in Orthostatic Hypotension Questionnaire (OHQ) composite score from baseline to Week 8. Key secondary variables included dizziness/lightheadedness score (OHQ item 1) and patient-reported falls.
Among 24 droxidopa and 27 placebo recipients, mean OHQ composite-score change at Week 8 was -2.2 versus -2.1 (p = 0.98); in response to this pre-planned futility analysis, the study was temporarily stopped and all data from these patients were considered exploratory. At Week 1, mean dizziness/lightheadedness score change favored droxidopa by 1.5 units (p = 0.24), with subsequent numerical differences favoring droxidopa throughout the observation period, and at Week 1, mean standing systolic blood-pressure change favored droxidopa by 12.5 mmHg (p = 0.04). Compared with placebo, the droxidopa group exhibited an approximately 50% lower rate of reported falls (p = 0.16) and fall-related injuries (post-hoc analysis).
This exploratory analysis of a small dataset failed to show benefit of droxidopa, as compared with placebo by the primary endpoint. Nonetheless, there were signals of potential benefit for nOH, including improvement in dizziness/lightheadedness and reduction in falls, meriting evaluation in further trials.
神经源性直立性低血压(nOH)在帕金森病(PD)中很常见,表现为无法产生与体位变化相适应的去甲肾上腺素反应。屈昔多巴(L-苏式-3,4-二羟基苯丝氨酸)是一种口服去甲肾上腺素前体药物。
对屈昔多巴治疗帕金森病合并神经源性直立性低血压的多中心、随机、双盲、安慰剂对照3期试验中最初入组患者的中期分析(ClinicalTrials.gov标识符:NCT01176240)。
记录有神经源性直立性低血压的帕金森病患者接受≤2周的双盲屈昔多巴或安慰剂剂量优化,随后进行8周的维持治疗(每日3次,每次100 - 600 mg)。主要疗效指标是从基线到第8周直立性低血压问卷(OHQ)综合评分的变化。关键次要变量包括头晕/头重脚轻评分(OHQ项目1)和患者报告的跌倒情况。
在24名接受屈昔多巴治疗和27名接受安慰剂治疗的患者中,第8周时OHQ综合评分的平均变化分别为-2.2和-2.1(p = 0.98);针对这一预先计划的无效性分析,该研究暂时停止,这些患者的所有数据均被视为探索性数据。在第1周时,头晕/头重脚轻评分的平均变化有利于屈昔多巴,差值为1.5个单位(p = 0.24),在整个观察期内后续的数值差异均有利于屈昔多巴,且在第1周时,站立位收缩压的平均变化有利于屈昔多巴,差值为12.5 mmHg(p = 0.04)。与安慰剂相比,屈昔多巴组报告的跌倒发生率(事后分析)和跌倒相关损伤发生率降低了约50%(p = 0.16)。
对一个小数据集的这项探索性分析未能显示与安慰剂相比屈昔多巴有获益,以主要终点衡量。尽管如此,对于神经源性直立性低血压仍有潜在获益信号,包括头晕/头重脚轻症状改善和跌倒减少,值得在进一步试验中进行评估。