Disease modifying therapies in relapsing-remitting multiple sclerosis: A systematic review and network meta-analysis

被引:45
|
作者
Liu, Zhuoyi [1 ]
Liao, Qiao [2 ]
Wen, Haicheng [3 ]
Zhang, Yihao [4 ]
机构
[1] Cent South Univ, Xiangya Hosp, Dept Anesthesiol, Changsha, Hunan, Peoples R China
[2] Cent South Univ, Xiangya Hosp, Dept Neurol, Changsha, Hunan, Peoples R China
[3] Cent South Univ, Xiangya Hosp, Changsha, Hunan, Peoples R China
[4] Southern Med Univ, Nanfang Hosp, Dept Gen Surg, Guangzhou, Guangdong, Peoples R China
关键词
Relapsing-remitting multiple sclerosis; Disease modifying therapy; Network meta-analysis; PLACEBO-CONTROLLED TRIAL; INTERFERON BETA-1A; CONTROLLED PHASE-3; DOUBLE-BLIND; ORAL LAQUINIMOD; ALEMTUZUMAB; EFFICACY; MULTICENTER; TERIFLUNOMIDE; NATALIZUMAB;
D O I
10.1016/j.autrev.2021.102826
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: To compare the efficacy and compliance of up-to-date disease modifying therapies (DMTs) in patients with remitting-relapsing MS (RRMS). Methods: We searched PubMed, EMBASE and Cochrane Library for eligible studies. Annualized relapse rate, discontinuation due to adverse events (AEs) were assessed as primary outcomes. Sensitivity analysis and inconsistency detection were performed to evaluated whether exclusion of high-risk studies affected the validity. Risk of bias was assessed using Cochrane's Risk-of-Bias Tool 2. Surface under the cumulative ranking curve (SUCRA) was used to estimate the rankings among different DMTs. Results: 21 studies were included for main report. Seven studies were evaluated as "high risk" and were therefore excluded. Exclusion of high-risk studies did not affect the validity of evidence. The risk of relapses for most DMTs except Betaseron 50 mu g was significantly lower comparing to placebo. Incompliance in patients treated with DMTs was not significantly increased comparing to placebo. Dimethyl fumarate and ocrelizumab had superiority in improving MRI outcomes. Ocrelizumab and ofatumumab had the largest reduction of risk in disability progression at 3 months. Referring to SUCRA, ofatumumab, alemtuzumab and natalizumab showed the best efficacy and compliance. Conclusion: The present study demonstrated the hierarchy of DMTs treating RRMS. Ofatumumab, alemtuzumab and natalizumab have superiority with respect to effectiveness and compliance. More studies are required to explore the long-term effect of DMTs. Our findings could provide helpful information and contribute to clinical treatment decision-making.
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页数:9
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