Safety and Efficacy of Methotrexate in Psoriasis: A Meta-Analysis of Published Trials.

BACKGROUND:Methotrexate (MTX) has been used to treat psoriasis for over half a century. Even so, clinical data characterising its efficacy and safety are sparse. OBJECTIVE:In order to enhance the available evidence, we conducted two meta-analyses, one for efficacy and one for safety outcomes, respec...

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Main Authors: Jonathan West, Simon Ogston, John Foerster
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4864230?pdf=render
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spelling doaj-b0a28495b02848c4aa2d7d261e88d17a2020-11-25T00:02:10ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-01115e015374010.1371/journal.pone.0153740Safety and Efficacy of Methotrexate in Psoriasis: A Meta-Analysis of Published Trials.Jonathan WestSimon OgstonJohn FoersterBACKGROUND:Methotrexate (MTX) has been used to treat psoriasis for over half a century. Even so, clinical data characterising its efficacy and safety are sparse. OBJECTIVE:In order to enhance the available evidence, we conducted two meta-analyses, one for efficacy and one for safety outcomes, respectively, according to PRISMA checklist. (Data sources, study criteria, and study synthesis methods are detailed in Methods). RESULTS:In terms of efficacy, only eleven studies met criteria for study design and passed a Cochrane risk of bias analysis. Based on this limited dataset, 45.2% [95% confidence interval 34.1-60.0] of patients achieve PASI75 at primary endpoint (12 or 16 weeks, respectively, n = 705 patients across all studies), compared to a calculated PASI75 of 4.4 [3.5-5.6] for placebo, yielding a relative risk of 10.2 [95% C.I. 7.1-14.7]. For safety outcomes, we extended the meta-analysis to include studies employing the same dose range of MTX for other chronic inflammatory conditions, e.g. rheumatoid arthritis, in order not to maximise capture of relevant safety data. Based on 2763 patient safety years, adverse events (AEs) were found treatment limiting in 6.9 ± 1.4% (mean ± s.e.) of patients treated for six months, with an adverse effect profile largely in line with that encountered in clinical practice. Finally, in order to facilitate prospective clinical audit and to help generate long-term treatment outcomes under real world conditions, we also developed an easy to use documentation form to be completed by patients without requirement for additional staff time. LIMITATIONS:Meta-analyses for efficacy and safety, respectively, employed non-identical selection criteria. CONCLUSIONS:These meta-analyses summarise currently available evidence on MTX in psoriasis and should be of use to gauge whether local results broadly fall within outcomes.http://europepmc.org/articles/PMC4864230?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Jonathan West
Simon Ogston
John Foerster
spellingShingle Jonathan West
Simon Ogston
John Foerster
Safety and Efficacy of Methotrexate in Psoriasis: A Meta-Analysis of Published Trials.
PLoS ONE
author_facet Jonathan West
Simon Ogston
John Foerster
author_sort Jonathan West
title Safety and Efficacy of Methotrexate in Psoriasis: A Meta-Analysis of Published Trials.
title_short Safety and Efficacy of Methotrexate in Psoriasis: A Meta-Analysis of Published Trials.
title_full Safety and Efficacy of Methotrexate in Psoriasis: A Meta-Analysis of Published Trials.
title_fullStr Safety and Efficacy of Methotrexate in Psoriasis: A Meta-Analysis of Published Trials.
title_full_unstemmed Safety and Efficacy of Methotrexate in Psoriasis: A Meta-Analysis of Published Trials.
title_sort safety and efficacy of methotrexate in psoriasis: a meta-analysis of published trials.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2016-01-01
description BACKGROUND:Methotrexate (MTX) has been used to treat psoriasis for over half a century. Even so, clinical data characterising its efficacy and safety are sparse. OBJECTIVE:In order to enhance the available evidence, we conducted two meta-analyses, one for efficacy and one for safety outcomes, respectively, according to PRISMA checklist. (Data sources, study criteria, and study synthesis methods are detailed in Methods). RESULTS:In terms of efficacy, only eleven studies met criteria for study design and passed a Cochrane risk of bias analysis. Based on this limited dataset, 45.2% [95% confidence interval 34.1-60.0] of patients achieve PASI75 at primary endpoint (12 or 16 weeks, respectively, n = 705 patients across all studies), compared to a calculated PASI75 of 4.4 [3.5-5.6] for placebo, yielding a relative risk of 10.2 [95% C.I. 7.1-14.7]. For safety outcomes, we extended the meta-analysis to include studies employing the same dose range of MTX for other chronic inflammatory conditions, e.g. rheumatoid arthritis, in order not to maximise capture of relevant safety data. Based on 2763 patient safety years, adverse events (AEs) were found treatment limiting in 6.9 ± 1.4% (mean ± s.e.) of patients treated for six months, with an adverse effect profile largely in line with that encountered in clinical practice. Finally, in order to facilitate prospective clinical audit and to help generate long-term treatment outcomes under real world conditions, we also developed an easy to use documentation form to be completed by patients without requirement for additional staff time. LIMITATIONS:Meta-analyses for efficacy and safety, respectively, employed non-identical selection criteria. CONCLUSIONS:These meta-analyses summarise currently available evidence on MTX in psoriasis and should be of use to gauge whether local results broadly fall within outcomes.
url http://europepmc.org/articles/PMC4864230?pdf=render
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