Efficacy and Safety of Tofacitinib, Baricitinib, and Upadacitinib for Rheumatoid Arthritis: A Systematic Review and Meta-Analysis

被引:83
作者
Wang, Faping [1 ,2 ]
Sun, Ling [3 ]
Wang, Shaohua [1 ]
Davis, John M. [4 ,5 ]
Matteson, Eric L. [4 ,5 ]
Murad, M. Hassan [6 ]
Luo, Fengming [2 ]
Vassallo, Robert [1 ]
机构
[1] Mayo Clin, Dept Med, Div Pulm & Crit Care Med, Coll Med & Sci, Rochester, MN 55902 USA
[2] Sichuan Univ, West China Hosp, Dept Resp & Crit Care Med, Chengdu 610041, Peoples R China
[3] Sichuan Univ, West China Hosp, Res Ctr Regenerat Med, Chengdu, Peoples R China
[4] Mayo Clin, Div Rheumatol, Coll Med & Sci, Rochester, MN 55902 USA
[5] Mayo Clin, Dept Hlth Sci Res, Coll Med & Sci, Rochester, MN 55902 USA
[6] Mayo Clin, Evidence Based Practice Ctr, Rochester, MN 55902 USA
关键词
JANUS KINASE INHIBITOR; INADEQUATE RESPONSE; JAK INHIBITOR; BACKGROUND METHOTREXATE; JAPANESE PATIENTS; DOUBLE-BLIND; PLACEBO; CP-690,550; MONOTHERAPY; DISEASE;
D O I
10.1016/j.mayocp.2020.01.039
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To assess the efficacy and safety profiles of different dosing regimens of tofacitinib, baricitinib, and upadacitinib, novel selective oral Janus activated kinase inhibitors, in rheumatoid arthritis (RA). Methods: Randomized controlled trials of tofacitinib (5 and 10 mg twice daily) baricitinib (2 and 4 mg daily), and upadacitinib (15 and 30 mg daily) in RA were identified from MEDLINE, EMBASE, and Cochrane databases through December 11, 2019. Random-effects models were used to estimate pooled mean differences and relative risks (RRs). American College of Rheumatology 20%, Health Assessment Questionnaire-Disability Index, adverse events, risk for infection, venous thromboembolic events, and malignancy were calculated. Results: Twenty trials with an overall low risk of bias involving 8982 patients were identified. Tofacitinib, baricitinib, and upadacitinib improved RA control as determined by American College of Rheumatology 20% (RR, 2.03; 95% CI, 1.87 to 2.20) and Health Assessment Questionnaire-Disability Index scores (mean differences, -0.31; 95% CI, -0.34 to -0.28) compared with placebo. Adverse events were more frequent with upadacitinib, 30 mg, daily (RR, 1.15; 95% CI, 1.02 to 1.30); upadacitinib, 15 mg, daily (RR, 1.14; 95% CI, 1.02 to 1.27); and baricitinib, 4 mg, daily (RR, 1.13; 95% CI, 1.02 to 1.24). The risk for infection was highest with tofacitinib, 10 mg, twice daily (RR, 2.75; 95% CI, 1.72 to 4.41), followed by upadacitinib, 15 mg, daily (RR, 1.35; 95% CI, 1.14 to 1.60) and baricitinib, 4 mg, daily (RR, 1.28; 95% CI, 1.12 to 1.45). Data for venous thromboembolic events were not available for tofacitinib or baricitinib, but there was no increase in risk with upadacitinib (15 mg daily: RR, 2.34; 95% CI, 0.34 to 15.92). Conclusion: Tofacitinib, baricitinib, and upadacitinib significantly improve RA control. Head-to-head Janus activated kinase inhibitor clinical trials are needed to further inform decision making. (C) 2020 Mayo Foundation for Medical Education and Research
引用
收藏
页码:1404 / 1419
页数:16
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