Efficacy and safety of bimekizumab in the treatment of psoriatic arthritis: a systematic review and meta-analysis

被引:2
作者
Su, Qin-Yi [1 ,2 ,3 ]
Yang, Liu [2 ,3 ,4 ]
Cao, Ting-Yu [2 ,3 ]
Dang, Hai-Ying [2 ,3 ]
Han, Zhuo-Chen [2 ,3 ]
Cao, Jia-Jing [2 ,3 ]
Zhang, He-Yi [2 ,3 ]
Cheng, Ting [1 ,2 ,3 ]
Zhang, Sheng-Xiao [1 ,2 ,3 ,6 ]
Huo, Yue-Hong [2 ,3 ,5 ]
机构
[1] Shanxi Med Univ, Dept Rheumatol, Hosp 2, Taiyuan, Shanxi, Peoples R China
[2] Shanxi Med Univ, Key Lab Cellular Physiol, Minist Educ, Taiyuan, Peoples R China
[3] Shanxi Med Univ, Shanxi Prov Key Lab Rheumatism Immune Microecol, Taiyuan, Shanxi, Peoples R China
[4] Shanxi Med Univ, Shanxi Bethune Hosp, Dept Gynecol & Obstet, Hosp 3, Taiyuan, Peoples R China
[5] Fifth Peoples Hosp Datong, Dept Rheumatol, Datong, Shanxi, Peoples R China
[6] 382 Wuyi Rd, Taiyuan, Shanxi, Peoples R China
基金
美国国家科学基金会;
关键词
Bimekizumab; IL-17; meta-analysis; psoriatic arthritis; biologic therapy; DOUBLE-BLIND; PHASE-3; TRIAL;
D O I
10.1080/14740338.2024.2343017
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Bimekizumab, a humanized monoclonal IgG1 antibody targeting both interleukin (IL)-17A and IL-17F, could be effective for treating Psoriatic arthritis (PsA). This study aimed to systematically evaluate the efficacy and safety of bimekizumab in the management of PsA. Research design and methods: A comprehensive literature search by August 2023 was performed through PubMed, Embase, Cochrane Controlled Register of Trials, and ClinicalTrials.gov. investigating the efficacy or safety data of bimekizumab in the treatment of PsA. Data was pooled using the random-effects models. Egger tests were used to evaluate potential publication bias. Results: A total of 4 RCTs, involving 892 PsA patients and 467 placebo controls, were included in this analysis. Bimekizumab significantly increased the rates of PASI75 and PASI100 compared with placebos [RR = 7.22, 95% CI (5.24, 9.94), p < 0.001; RR = 10.12, 95% CI (6.00, 17.09), p < 0.001]. The rate of overall adverse events was slightly higher in the bimekizumab group [RR = 1.42, 95% CI (1.05, 1.93) p = 0.023). However, there were fewer adverse severe drug reactions in the bimekizumab group compared to the placebo. Conclusion: Bimekizumab had a significant clinical benefit in managing PsA and an acceptable safety profile.
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页数:9
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