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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, resp...

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Autores principales: West, Jonathan, Ogston, Simon, Foerster, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4864230/
https://www.ncbi.nlm.nih.gov/pubmed/27168193
http://dx.doi.org/10.1371/journal.pone.0153740
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author West, Jonathan
Ogston, Simon
Foerster, John
author_facet West, Jonathan
Ogston, Simon
Foerster, John
author_sort West, Jonathan
collection PubMed
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.
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spelling pubmed-48642302016-05-18 Safety and Efficacy of Methotrexate in Psoriasis: A Meta-Analysis of Published Trials West, Jonathan Ogston, Simon Foerster, John PLoS One Research Article 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. Public Library of Science 2016-05-11 /pmc/articles/PMC4864230/ /pubmed/27168193 http://dx.doi.org/10.1371/journal.pone.0153740 Text en © 2016 West et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
West, Jonathan
Ogston, Simon
Foerster, John
Safety and Efficacy of Methotrexate in Psoriasis: A Meta-Analysis of Published Trials
title 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_short 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
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4864230/
https://www.ncbi.nlm.nih.gov/pubmed/27168193
http://dx.doi.org/10.1371/journal.pone.0153740
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