导航晚期帕金森病的治疗前景:从输注疗法到干细胞的全面回顾。

IF 5.4
Expert opinion on drug delivery Pub Date : 2025-10-01 Epub Date: 2025-08-01 DOI:10.1080/17425247.2025.2539962
Carmelo Fogliano, Leonardo Rigon, K Ray Chaudhuri, Karolina Popławska-Domaszewicz, Cristian Falup-Pecurariu, Iulia Murasan, Andrea Guerra, Michela Garon, Per Odin, Nobutaka Hattori, Angelo Antonini
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引用次数: 0

摘要

口服多巴胺能治疗是帕金森病(PD)治疗的基石。然而,口服左旋多巴作用的逐渐缩短,以及酶抑制剂和多巴胺激动剂的有限疗效,不能充分控制晚期帕金森病的运动和非运动并发症。在这个阶段,器械辅助治疗(dat),包括输液治疗,是有必要的,以保证足够的生活质量。涵盖领域:我们回顾了目前和即将推出的PD输注疗法,特别关注其疗效和安全性数据。此外,我们提供了当前的知识和开放的问题在患者选择和具体的数据选择的概述。专家意见:最近的EAN/MDS-ES指南建议输注治疗晚期PD,但仍然存在一些挑战,包括有限的获取,延迟转诊和患者犹豫。“5-2-1”标准和诸如MANAGE-PD之类的工具有助于早期识别合格的候选人,但治疗决策通常不能考虑患者的偏好。目前的趋势倾向于在运动波动出现并在残疾发生之前尽早实施dat。新出现的输液疗法(如foslevodopa-foscarbidopa)将促进这一趋势。加强临床试验中dat的可及性和包容性是关键优先事项。最后,再生疗法包括神经营养因子和多巴胺能神经元前体的膜层输注可能会改变晚期帕金森病的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Navigating the therapeutic landscape in advanced Parkinson's disease: a comprehensive review from infusion therapies to stem cells.

Introduction: Oral dopaminergic treatment is the cornerstone of Parkinson's disease (PD) management. However, progressive shortening of oral levodopa's effect, along with the limited efficacy of enzyme inhibitors and dopamine agonists, does not allow to adequately control motor and non-motor complications characterizing advanced PD. At this stage, device-aided therapies (DATs), including infusion treatments, are warranted to guarantee an adequate quality of life.

Areas covered: We review current and upcoming infusion therapies for PD, with a particular focus on their efficacy and safety data. Moreover, we provide an overview of current knowledge and open issues on patient selection and specific DAT choice.

Expert opinion: Recent EAN/MDS-ES guidelines suggest infusion therapies for advanced PD, yet several challenges remain, including limited access, delayed referrals, and patients' hesitancy. The '5-2-1' criteria and tools like MANAGE-PD aid early identification of eligible candidates, but treatment decisions often do not account for patients' preferences. Current trends favor early DATs implementation, as soon as motor fluctuations appear and before the disability onset. Emerging infusion therapies (e.g. foslevodopa-foscarbidopa) will boost this tendency. Enhancing DATs accessibility and inclusivity in clinical trials are key priorities. Finally, regenerative therapies including putaminal infusion of neurotrophic factors and dopaminergic neuron precursors may transform advanced PD care.

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