Translational Neurotherapeutics Program, Laboratory for Dementia and Parkinsonism, Department of Neurology, Georgetown University Medical Center, Washington, District of Columbia, USA.
Movement Disorders Clinic, Department of Neurology, MedStar Georgetown University Hospital, Washington, District of Columbia, USA.
Mov Disord. 2021 Mar;36(3):740-749. doi: 10.1002/mds.28389. Epub 2020 Nov 20.
Nilotinib is US Food and Drug Administration-approved for leukemia, and this open-label study investigated the safety, tolerability, and potential clinical effects of nilotinib in medically optimized patients with Parkinson's disease.
Safety and tolerability were the primary objectives, and clinical outcomes were exploratory.
A total of 63 patients completed a 15-month phase 2, double-blind, placebo-controlled study and were rerandomized 1:1 into an open-label study of nilotinib 150 mg versus 300 mg for 12 months.
Nilotinib was safe and tolerated, and no adverse effects seemed to be related to the drug, and no differences in adverse events were observed between groups. Exploratory clinical outcomes showed that nilotinib 300 mg was remarkably stable from baseline to 27 months using partial and total Unified Parkinson's Disease Scale (UPDRS). Nilotinib 150 mg versus 300 mg, significantly declined using partial or the sum of UPDRS Parts I and II. There was no significant difference in nilotinib 150 mg versus 300 mg using UPDRS Part III (on levodopa) and total UPDRS Parts I to III. Subgroup analysis showed that late-start nilotinib 150 mg significantly worsened using the sum of UPDRS Parts II + III and total UPDRS Parts I to III compared with late-start nilotinib 300 mg. Quality of life using the Parkinson's Disease Questionnaire in nilotinib 150 mg significantly declined between 15 and 27 months compared with nilotinib 300 mg, and there was no change in cognition using the Montreal Cognitive Assessment between groups.
This study provides evidence that nilotinib is safe and tolerated in Parkinson's disease. The exploratory clinical data will inform an adequately powered larger study to evaluate the efficacy of nilotinib 300 mg in Parkinson's disease. © 2020 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
尼洛替尼已获得美国食品和药物管理局批准用于治疗白血病,本开放性研究旨在调查尼洛替尼在经过医学优化的帕金森病患者中的安全性、耐受性和潜在临床疗效。
安全性和耐受性是主要目标,临床结果是探索性的。
共有 63 例患者完成了一项为期 15 个月的 2 期、双盲、安慰剂对照研究,并被 1:1 重新随机分为尼洛替尼 150mg 与 300mg 组,分别进行为期 12 个月的开放性研究。
尼洛替尼安全耐受,无药物相关不良事件,组间不良反应无差异。探索性临床结果显示,尼洛替尼 300mg 从基线到 27 个月时使用部分和总统一帕金森病评定量表(UPDRS)均显著稳定。与尼洛替尼 150mg 相比,尼洛替尼 300mg 部分或 UPDRS 第一和第二部分总和显著下降。尼洛替尼 150mg 与 300mg 对 UPDRS 第三部分(左旋多巴)和 UPDRS 第一至第三部分总和无显著差异。亚组分析显示,与尼洛替尼 300mg 相比,晚期开始使用尼洛替尼 150mg 的患者 UPDRS 第二和第三部分总和以及 UPDRS 第一至第三部分总和显著恶化。尼洛替尼 150mg 组在 15 至 27 个月期间使用帕金森病问卷的生活质量显著下降,而两组间认知测试蒙特利尔认知评估无变化。
本研究为尼洛替尼在帕金森病中的安全性和耐受性提供了证据。探索性临床数据将为评估尼洛替尼 300mg 在帕金森病中的疗效提供信息,我们将进行一项更大规模的研究。© 2020 作者。运动障碍由 Wiley Periodicals LLC 代表国际帕金森病和运动障碍学会出版。