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Immunosuppressive and monoclonal antibody treatment for myasthenia gravis: A network meta‐analysis
BACKGROUND: We intended to compare and rank all the immunotherapies including immunosuppressant agents or monoclonal antibodies for myasthenia gravis (MG). METHODS: A network meta‐analysis was performed to synthesize the direct evidence and indirect evidence. Quantitative MG score (QMGS) was defined...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488910/ https://www.ncbi.nlm.nih.gov/pubmed/30809966 http://dx.doi.org/10.1111/cns.13110 |
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author | Wang, Liang Huan, Xiao Xi, Jian‐Ying Wu, Hui Zhou, Lei Lu, Jia‐Hong Zhang, Tian‐Song Zhao, Chong‐Bo |
author_facet | Wang, Liang Huan, Xiao Xi, Jian‐Ying Wu, Hui Zhou, Lei Lu, Jia‐Hong Zhang, Tian‐Song Zhao, Chong‐Bo |
author_sort | Wang, Liang |
collection | PubMed |
description | BACKGROUND: We intended to compare and rank all the immunotherapies including immunosuppressant agents or monoclonal antibodies for myasthenia gravis (MG). METHODS: A network meta‐analysis was performed to synthesize the direct evidence and indirect evidence. Quantitative MG score (QMGS) was defined as the primary outcome. The secondary outcomes included the glucocorticoid reduction and hazard ratios (HR) from the counts of adverse events (AEs). RESULTS: We identified 14 studies including 808 MG patients. For the primary outcome, cyclosporine A (CsA) was hierarchically the best with statistical significances of −1.18 (−1.81, −0.59) vs placebo (PLA), −0.98 (−1.72, −0.23) vs mycophenolate mofetil, and −0.77 (−1.57, −0.032) vs tacrolimus (TAC). When the intervention periods were controlled, both eculizumab (ECZ) of −1.50 (−2.81, −0.18) and CsA of −1.23 (−1.81, −0.64) vs PLA reached a statistical significance. Belimumab and ECZ ranked the most tolerable therapies while CsA of 2.41 (0.58, 10.01) ranked the last vs PLA. CONCLUSION: These findings demonstrated that ECZ represented the most effective and tolerable therapeutic alternative to be recommended for refractory MG. TAC may be a beneficial therapy to treat MG extensively while the efficacy of CsA and cyclophosphamide may be limited by their multiple or severe AEs. |
format | Online Article Text |
id | pubmed-6488910 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64889102019-06-26 Immunosuppressive and monoclonal antibody treatment for myasthenia gravis: A network meta‐analysis Wang, Liang Huan, Xiao Xi, Jian‐Ying Wu, Hui Zhou, Lei Lu, Jia‐Hong Zhang, Tian‐Song Zhao, Chong‐Bo CNS Neurosci Ther Meta‐analysis BACKGROUND: We intended to compare and rank all the immunotherapies including immunosuppressant agents or monoclonal antibodies for myasthenia gravis (MG). METHODS: A network meta‐analysis was performed to synthesize the direct evidence and indirect evidence. Quantitative MG score (QMGS) was defined as the primary outcome. The secondary outcomes included the glucocorticoid reduction and hazard ratios (HR) from the counts of adverse events (AEs). RESULTS: We identified 14 studies including 808 MG patients. For the primary outcome, cyclosporine A (CsA) was hierarchically the best with statistical significances of −1.18 (−1.81, −0.59) vs placebo (PLA), −0.98 (−1.72, −0.23) vs mycophenolate mofetil, and −0.77 (−1.57, −0.032) vs tacrolimus (TAC). When the intervention periods were controlled, both eculizumab (ECZ) of −1.50 (−2.81, −0.18) and CsA of −1.23 (−1.81, −0.64) vs PLA reached a statistical significance. Belimumab and ECZ ranked the most tolerable therapies while CsA of 2.41 (0.58, 10.01) ranked the last vs PLA. CONCLUSION: These findings demonstrated that ECZ represented the most effective and tolerable therapeutic alternative to be recommended for refractory MG. TAC may be a beneficial therapy to treat MG extensively while the efficacy of CsA and cyclophosphamide may be limited by their multiple or severe AEs. John Wiley and Sons Inc. 2019-02-26 /pmc/articles/PMC6488910/ /pubmed/30809966 http://dx.doi.org/10.1111/cns.13110 Text en © 2019 The Authors. CNS Neuroscience & Therapeutics Published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Meta‐analysis Wang, Liang Huan, Xiao Xi, Jian‐Ying Wu, Hui Zhou, Lei Lu, Jia‐Hong Zhang, Tian‐Song Zhao, Chong‐Bo Immunosuppressive and monoclonal antibody treatment for myasthenia gravis: A network meta‐analysis |
title | Immunosuppressive and monoclonal antibody treatment for myasthenia gravis: A network meta‐analysis |
title_full | Immunosuppressive and monoclonal antibody treatment for myasthenia gravis: A network meta‐analysis |
title_fullStr | Immunosuppressive and monoclonal antibody treatment for myasthenia gravis: A network meta‐analysis |
title_full_unstemmed | Immunosuppressive and monoclonal antibody treatment for myasthenia gravis: A network meta‐analysis |
title_short | Immunosuppressive and monoclonal antibody treatment for myasthenia gravis: A network meta‐analysis |
title_sort | immunosuppressive and monoclonal antibody treatment for myasthenia gravis: a network meta‐analysis |
topic | Meta‐analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488910/ https://www.ncbi.nlm.nih.gov/pubmed/30809966 http://dx.doi.org/10.1111/cns.13110 |
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