Parkinson's Disease and Movement Disorders Center, Department of Neurology, University of South Florida, Tampa, FL.
Columbia University Medical Center, New York, NY.
Clin Neuropharmacol. 2023;46(2):66-78. doi: 10.1097/WNF.0000000000000540. Epub 2023 Jan 29.
Oral levodopa is the most effective treatment for Parkinson disease, but OFF periods emerge over time. Gastrointestinal dysfunction and food effects impact levodopa absorption, contributing to unpredictable control of OFF periods. Inhaled levodopa powder (Inbrija) is approved for on-demand treatment of OFF periods in patients receiving oral levodopa-dopa decarboxylase inhibitors. The 84-mg dose is administered via a breath-actuated inhaler. It provides pulmonary delivery of levodopa to the systemic circulation and is taken when a patient has an OFF period in between doses of regular oral levodopa medication. The pivotal SPAN-PD trial in patients experiencing OFF periods on oral dopaminergic therapy showed that levodopa inhalation powder 84 mg produced significant improvement in Unified Parkinson Disease Rating Scale Part III score, as measured 30 minutes postdose at week 12, and improvement was seen as early as 10 minutes. More patients in the levodopa inhalation powder group turned ON within 60 minutes of treatment and remained ON at 60 minutes than in the placebo group. Levodopa inhalation powder can also be used to treat early-morning OFF periods and, when used for up to 12 months, produced no clinically significant differences in pulmonary function compared with an untreated cohort. Levodopa inhalation powder 84 mg increased plasma levodopa concentration rapidly and with less variability than oral levodopa/carbidopa (25/100 mg). Most common adverse event associated with levodopa inhalation powder is cough, found in ~15% of patients in the SPAN-PD trial; otherwise, reported adverse events were consistent with those known to be associated with oral levodopa.
口服左旋多巴是治疗帕金森病最有效的方法,但随着时间的推移,会出现“OFF”期。胃肠道功能障碍和食物效应对左旋多巴的吸收有影响,导致“OFF”期的控制变得不可预测。吸入性左旋多巴粉(Inbrija)已被批准用于按需治疗正在接受口服左旋多巴-多巴脱羧酶抑制剂治疗的患者的“OFF”期。84 毫克剂量通过呼吸驱动吸入器给药。它将左旋多巴递送至全身循环,并在患者在口服常规左旋多巴药物之间的“OFF”期时使用。在接受口服多巴胺能治疗出现“OFF”期的患者中进行的关键 SPAN-PD 试验表明,左旋多巴吸入粉 84 毫克可显著改善统一帕金森病评定量表第三部分评分,在第 12 周剂量后 30 分钟测量时,改善情况早在 10 分钟即可出现。在治疗后 60 分钟内,左旋多巴吸入粉组中有更多的患者转为“ON”状态,并且在 60 分钟时仍保持“ON”状态,而安慰剂组则较少。左旋多巴吸入粉还可用于治疗清晨的“OFF”期,并且在使用长达 12 个月的时间内,与未治疗组相比,对肺功能没有产生临床上显著的差异。与口服左旋多巴/卡比多巴(25/100 毫克)相比,左旋多巴吸入粉 84 毫克可快速且更稳定地提高血浆左旋多巴浓度。与左旋多巴吸入粉相关的最常见不良事件是咳嗽,在 SPAN-PD 试验中约有 15%的患者出现;否则,报告的不良事件与已知与口服左旋多巴相关的不良事件一致。