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Open-label trial of anti-TNF-alpha in dermato- and polymyositis treated concomitantly with methotrexate

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dc.contributor.author Hengstman, GJD en
dc.contributor.author De Bleecker, JL en
dc.contributor.author Feist, E en
dc.contributor.author Vissing, J en
dc.contributor.author Denton, CP en
dc.contributor.author Manoussakis, MN en
dc.contributor.author Jensen, HS en
dc.contributor.author van Engelen, BGM en
dc.contributor.author van den Hoogen, FHJ en
dc.date.accessioned 2014-03-01T01:57:34Z
dc.date.available 2014-03-01T01:57:34Z
dc.date.issued 2008 en
dc.identifier.issn 0014-3022 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/28434
dc.subject myositis en
dc.subject open-label trial en
dc.subject methotrexate en
dc.subject anti-TNF therapy en
dc.subject.classification Clinical Neurology en
dc.subject.classification Neurosciences en
dc.subject.other NECROSIS-FACTOR-ALPHA en
dc.subject.other INFLAMMATORY MYOPATHIES en
dc.subject.other RECEPTORS en
dc.title Open-label trial of anti-TNF-alpha in dermato- and polymyositis treated concomitantly with methotrexate en
heal.type journalArticle en
heal.language English en
heal.publicationDate 2008 en
heal.abstract Background/Aims: To determine the efficacy of infliximab combined with weekly methotrexate in drug-naive recent-onset dermatomyositis and polymyositis. Methods: A multi-centre open-label controlled trial was conducted. Disease activity was assessed using patient's and physician's disease activity assessment, manual muscle testing (MMT), hand-held dynamometry, and serum CK. The primary objective was to assess the efficacy using MMT after a period of 26 weeks. Results: The study was terminated prematurely because of a low inclusion rate and a high drop-out rate due to disease progression and the occurrence of an infusion reaction. The few patients who did reach the primary endpoint showed improvement in all aspects studied. Conclusion: Infliximab combined with weekly methotrexate might be safe and well tolerated in a small subgroup of patients with drug-naive recent-onset myositis. At present, we do not advocate the use of this treatment because treatment response cannot be predicted beforehand. Copyright (C) 2008 S. Karger AG, Basel. en
heal.publisher KARGER en
heal.journalName EUROPEAN NEUROLOGY en
dc.identifier.isi ISI:000253371700009 en
dc.identifier.volume 59 en
dc.identifier.issue 3-4 en
dc.identifier.spage 159 en
dc.identifier.epage 163 en


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