Literature DB >> 23278581

Treatment in Lambert-Eaton myasthenic syndrome.

Paul Maddison1.   

Abstract

Besides antitumor therapy for patients with the paraneoplastic form of Lambert-Eaton myasthenic syndrome (LEMS), the mainstay of symptomatic treatment in LEMS is 3,4-diaminopyridine (3,4-DAP). Data from four randomized, placebo-controlled trials have revealed that muscle strength scores increased significantly with 3,4-DAP. A limited meta-analysis performed on two trials using the Quantitative Myasthenia Gravis score indicated that the clinical benefits seen were modest. Meta-analysis of the mean change in compound muscle action potential amplitude following 3,4-DAP treatment revealed a significant improvement compared to placebo. However, most patients with noncancer LEMS require long-term immunosuppression, usually with prednisolone and azathioprine. A single crossover study has previously shown significant short-term benefit in limb strength following intravenous immunoglobulin, and there are isolated case reports of medium term benefit from rituximab. Overall, a combination of symptomatic treatment with 3,4-DAP and immunosuppression, with or without antitumor therapy, is often successful for most LEMS patients, with other more aggressive regimens rarely needed.
© 2012 New York Academy of Sciences.

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Year:  2012        PMID: 23278581     DOI: 10.1111/j.1749-6632.2012.06769.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  4 in total

1.  Successful treatment of Lambert-Eaton myasthenic syndrome in a small cell lung cancer patient using 3,4-diaminopyridine: A case report.

Authors:  Jae-Won Hyun; Su-Hyun Kim; In Hye Jeong; Heung Tae Kim; Ho Jin Kim
Journal:  Oncol Lett       Date:  2016-01-18       Impact factor: 2.967

Review 2.  Synaptic Pathophysiology and Treatment of Lambert-Eaton Myasthenic Syndrome.

Authors:  Tyler B Tarr; Peter Wipf; Stephen D Meriney
Journal:  Mol Neurobiol       Date:  2014-09-09       Impact factor: 5.590

3.  A mutation in CaV2.1 linked to a severe neurodevelopmental disorder impairs channel gating.

Authors:  Sidharth Tyagi; Tyler R Bendrick; Dilyana Filipova; Symeon Papadopoulos; Roger A Bannister
Journal:  J Gen Physiol       Date:  2019-04-23       Impact factor: 4.086

4.  The European LEMS Registry: Baseline Demographics and Treatment Approaches.

Authors:  Renato Mantegazza; Andreas Meisel; Joern P Sieb; Gwendal Le Masson; Claude Desnuelle; Mirko Essing
Journal:  Neurol Ther       Date:  2015-11-02
  4 in total

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