Comparative efficacy and safety of disease-modifying therapies in patients with relapsing multiple sclerosis: A systematic review and network meta-analysis

被引:9
|
作者
Chen, Chaoyang [4 ]
Zhang, Enyao [4 ]
Zhu, Chunsu [4 ]
Wei, Ran [2 ]
Ma, Lingyun [3 ]
Dong, Xiu [4 ]
Li, Ruoming [4 ]
Sun, Feng [5 ]
Zhou, Ying [4 ]
Cui, Yimin [1 ,3 ,4 ,5 ,6 ]
Liu, Zhenming [1 ,3 ,4 ,5 ,6 ]
机构
[1] Peking Univ Hlth Sci Ctr Xueyuan Rd, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Haidian Dist, Beijing 100191, Peoples R China
[2] Peking Univ First Hosp, Dept Pharm, Beijing, Peoples R China
[3] Peking Univ First Hosp, Dept Pharm, Beijing, Peoples R China
[4] Peking Univ First Hosp, Dept Pharm, Beijing, Peoples R China
[5] Peking Univ, Sch Publ Hlth, Dept Epidemiol & Biostatist, Beijing, Peoples R China
[6] Peking Univ Hlth Sci Ctr, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Beijing, Peoples R China
关键词
PLACEBO-CONTROLLED TRIAL; DOUBLE-BLIND; INTERFERON BETA-1A; CONTROLLED PHASE-3; GLATIRAMER ACETATE; ORAL FINGOLIMOD; SUBCUTANEOUS INTERFERON-BETA-1A; INTRAMUSCULAR INTERFERON; ALEMTUZUMAB; TERIFLUNOMIDE;
D O I
10.1016/j.japh.2022.07.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Currently, 19 disease-modifying therapies (DMTs) have been approved for the treatment of patients with relapsing forms of multiple sclerosis (RMS). Objective: The objective of this study was to conduct a systematic review and network meta-analysis to evaluate the efficacy and safety of DMTs in adults with RMS. Methods: We searched PubMed, Embase, the Cochrane Central Register of Controlled Trials, ClinicalTrials.gov, the Food and Drug Administration, and European Medicines Agency websites for randomized controlled trials (RCTs) (from inception to July 2021). Eligible RCTs evaluated approved treatments for RMS as monotherapy and reported at least one of the primary outcome measures of interest. The primary outcome was efficacy (annualized relapse rate and 12-week confirmed disability progression) and safety (serious adverse events [AEs] and discontinuation due to AEs). We assessed the risk of bias (RoB) of included studies using the Cochrane RoB tool version 2.0 (https://www.bmj.com/content/343/bmj.d5928) for RCTs. Surface under the cumulative ranking (SUCRA) was used to rank therapies and to assess quality of general evidence, respectively. The Grading of Recommendations Assessment, Development and Evaluation framework was used to rank therapies and to assess quality of general evidence. Results: A total of 43 records represent 45 RCTs selected for network meta-analysis. In total, 30,720 participants (median of 732; interquartile range: 248-931) were included, of which 67% were female. By SUCRA analysis, alemtuzumab (94.3%) presented the highest probability of being the best alternative for annualized relapse rate, whereas ofatumumab (93.5%) presented the highest probability of being the best alternative for 12-week confirmed disability progression. Interferon beta-1b subcutaneous (87.0%) presented the highest probability of the best safety among all DMTs for serious AEs, whereas alemtuzumab (92.4%) presented the highest probability of the best safety among all DMTs for discontinuation due to AEs. Conclusion: Network meta-analysis shows that alemtuzumab and ofatumumab present the highest efficacy among DMTs. Because there is little difference between these probabilities for many treatments, health professionals should use clinical shared decision making when formulating treatment plans with patients. (c) 2022 American Pharmacists Association((R)). Published by Elsevier Inc. All rights reserved.
引用
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页码:8 / +
页数:38
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