兰伯特-伊顿肌无力综合征的药物治疗

Wisse Bakker, L. Remijn-Nelissen, Kirsten J.M. Schimmel, M. Tannemaat, J. Verschuuren, T. van Gelder
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摘要

兰伯特-伊顿肌无力综合征(LEMS)是一种非常罕见的抗体介导的神经肌肉交界处自身免疫性疾病。治疗可分为对症治疗和免疫抑制治疗。阿米福定对症治疗是目前唯一被批准用于LEMS患者的治疗方法。在荷兰,首选药物是缓释制剂中的氨福定碱,而不是目前批准的磷酸氨福定。该配方成本较低,由于峰值浓度较低,可能更安全。用于LEMS患者的其他治疗是根据重症肌无力患者的经验开出的。在许多情况下,添加吡哆斯的明作为对症治疗。在几乎一半的患者开始免疫抑制治疗,主要是皮质类固醇与或不硫唑嘌呤。静脉注射免疫球蛋白和血浆置换是紧急治疗方法。目前还没有针对LEMS患者的新疗法的随机临床试验正在进行或宣布,尽管多种重症肌无力的新疗法正在研究中。这些未来的治疗方法可以区分为对症药物和免疫调节药物。免疫调节药物可进一步分为针对b细胞的早期药物、针对循环抗体的后期药物和具有疾病特异性靶点的靶向治疗药物。一些早期和晚期免疫调节药物在重症肌无力中显示出良好的效果,尽管高成本和不确定的长期安全性可能限制了将这些药物纳入LEMS治疗指南。由于该病的罕见性,目前缺乏针对LEMS患者的临床试验,我们建议对潜在新疗法的未来试验提出以下要求:适当时进行多中心或n-of-1试验,以获得足够的疗效,交叉设计以减少患者数量,并使用LEMS特异性定量主要结局指标,如3TUG评分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacological treatment of Lambert-Eaton Myasthenic Syndrome
Lambert-Eaton myasthenic syndrome (LEMS) is a very rare antibody-mediated autoimmune disease of the neuromuscular junction. Therapy can be divided in symptomatic treatment and immunosuppressive treatment. Symptomatic treatment with amifampridine is the only therapy currently authorized for use in LEMS patients. In the Netherlands the first choice drug is amifampridine base in an extended release formulation instead of the currently authorized amifampridine phosphate. This formulation has lower costs and is possibly safer due to lower peak concentrations. Other therapy used in LEMS patients is prescribed off-label and is based on experience in patients with myasthenia gravis. In many cases pyridostigmine is added as symptomatic treatment. In almost half of patients immunosuppressive therapy is started, mostly corticosteroids with or without azathioprine. Intravenous immunoglobulins and plasma exchange are used as emergency treatment. Currently no randomized clinical trials with new therapies are ongoing or announced in patients with LEMS, although multiple new therapies for myasthenia gravis are being investigated. These future therapies can be differentiated in symptomatic and immunomodulating drugs. The immunomodulating drugs can be further differentiated in early stage drugs which target the B-cell, later stage drugs which target the circulating antibodies and targeted therapy which have a disease-specific target. Some early and later stage immunomodulating drugs show promising results in myasthenia gravis although high cost and uncertain long term safety may be limiting for incorporating these drugs in LEMS treatment guidelines. Clinical trials in LEMS patients are lacking due to the rarity of the disease and we suggest the following requirements for future trials of potential new treatments: Sufficient power by performing multicenter or n-of-1 trials when appropriate, a cross-over design to reduce the number of patients and using a LEMS-specific quantitative primary outcome measure like the 3TUG score.
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