PMID- 30809966 OWN - NLM STAT- MEDLINE DCOM- 20200817 LR - 20210109 IS - 1755-5949 (Electronic) IS - 1755-5930 (Print) IS - 1755-5930 (Linking) VI - 25 IP - 5 DP - 2019 May TI - Immunosuppressive and monoclonal antibody treatment for myasthenia gravis: A network meta-analysis. PG - 647-658 LID - 10.1111/cns.13110 [doi] AB - 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. CI - (c) 2019 The Authors. CNS Neuroscience & Therapeutics Published by John Wiley & Sons Ltd. FAU - Wang, Liang AU - Wang L AD - Department of Neurology, Huashan Hospital, Fudan University, Shanghai, China. FAU - Huan, Xiao AU - Huan X AD - Department of Neurology, Huashan Hospital, Fudan University, Shanghai, China. FAU - Xi, Jian-Ying AU - Xi JY AD - Department of Neurology, Huashan Hospital, Fudan University, Shanghai, China. FAU - Wu, Hui AU - Wu H AD - Department of Neurology, Jing'an District Centre Hospital of Shanghai, Fudan University, Shanghai, China. FAU - Zhou, Lei AU - Zhou L AD - Department of Neurology, Huashan Hospital, Fudan University, Shanghai, China. FAU - Lu, Jia-Hong AU - Lu JH AD - Department of Neurology, Huashan Hospital, Fudan University, Shanghai, China. FAU - Zhang, Tian-Song AU - Zhang TS AD - Department of Chinese Traditional Medicine, Jing'an District Centre Hospital of Shanghai, Fudan University, Shanghai, China. FAU - Zhao, Chong-Bo AU - Zhao CB AUID- ORCID: 0000-0001-9481-1418 AD - Department of Neurology, Huashan Hospital, Fudan University, Shanghai, China. AD - Department of Neurology, Jing'an District Centre Hospital of Shanghai, Fudan University, Shanghai, China. LA - eng PT - Journal Article PT - Meta-Analysis PT - Research Support, Non-U.S. Gov't DEP - 20190226 PL - England TA - CNS Neurosci Ther JT - CNS neuroscience & therapeutics JID - 101473265 RN - 0 (Antibodies, Monoclonal) RN - 0 (Immunosuppressive Agents) SB - IM MH - Antibodies, Monoclonal/*therapeutic use MH - Humans MH - Immunosuppressive Agents/*therapeutic use MH - Myasthenia Gravis/*therapy MH - Network Meta-Analysis PMC - PMC6488910 OTO - NOTNLM OT - immunosuppressive agents OT - immunotherapy OT - monoclonal antibody OT - myasthenia gravis COIS- The authors declare that they have no conflict of interest. EDAT- 2019/02/28 06:00 MHDA- 2020/08/18 06:00 PMCR- 2019/02/26 CRDT- 2019/02/28 06:00 PHST- 2018/12/04 00:00 [received] PHST- 2019/01/22 00:00 [revised] PHST- 2019/01/23 00:00 [accepted] PHST- 2019/02/28 06:00 [pubmed] PHST- 2020/08/18 06:00 [medline] PHST- 2019/02/28 06:00 [entrez] PHST- 2019/02/26 00:00 [pmc-release] AID - CNS13110 [pii] AID - 10.1111/cns.13110 [doi] PST - ppublish SO - CNS Neurosci Ther. 2019 May;25(5):647-658. doi: 10.1111/cns.13110. Epub 2019 Feb 26.