TY - JOUR
T1 - Efficacy and Safety of Tofacitinib, Baricitinib, and Upadacitinib for Rheumatoid Arthritis
T2 - A Systematic Review and Meta-Analysis
AU - Wang, Faping
AU - Sun, Ling
AU - Wang, Shaohua
AU - Davis, John M.
AU - Matteson, Eric L.
AU - Murad, M. Hassan
AU - Luo, Fengming
AU - Vassallo, Robert
N1 - Funding Information:
Grant Support: This study was supported by National Nature Science Foundation of China grant (NSFC no. 81470268, no. 81770072), Ministry of Science and Technology of the People's Republic of China (no. 2017YFC0107805), Science and Technology Support Program of Sichuan province (no. 2016SZ0002), Chengdu Science and Technology Bureau (no. 2018-CY02-00064-GX), and 1.3.5 project for disciplines of excellence, West China Hospital, Sichuan University (ZYJC18021).Potential Competing Interests: Dr Vassallo has received research grant support from Pfizer, Bristol Myers Squibb, and Sun Pharmaceuticals. Dr Matteson has received research grant support from Pfizer, Boehringer-Ingelheim, Bristol Myers Squibb, and Sun Pharmaceuticals and serves on Advisory Boards for Boehringer-Ingelheim, Gilead Sciences, and Simply Speaking. Dr Davis has received research grant support from Pfizer and has served on advisory boards for Abbvie and Sanofi Genzyme. The remaining authors report no competing interests.
Funding Information:
Grant Support: This study was supported by National Nature Science Foundation of China grant (NSFC no. 81470268 , no. 81770072 ), Ministry of Science and Technology of the People's Republic of China (no. 2017YFC0107805 ), Science and Technology Support Program of Sichuan province (no. 2016SZ0002 ), Chengdu Science and Technology Bureau (no. 2018-CY02-00064-GX ), and 1.3.5 project for disciplines of excellence, West China Hospital, Sichuan University (ZYJC18021).
Publisher Copyright:
© 2020 Mayo Foundation for Medical Education and Research
PY - 2020/7
Y1 - 2020/7
N2 - 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.
AB - 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.
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U2 - 10.1016/j.mayocp.2020.01.039
DO - 10.1016/j.mayocp.2020.01.039
M3 - Article
C2 - 32499126
AN - SCOPUS:85085637469
SN - 0025-6196
VL - 95
SP - 1404
EP - 1419
JO - Mayo Clinic Proceedings
JF - Mayo Clinic Proceedings
IS - 7
ER -