Literature DB >> 33064892

Risk of Venous Thromboembolism Associated With Tofacitinib and Baricitinib: A Systematic Review and Indirect Meta-Analysis.

Teresa Giménez Poderós1, Sara Gallardo Borge2, Pedro Vazquez-Ferreiro3.   

Abstract

To conduct a systematic review and meta-analysis investigating the effect of tofacitinib and baricitinib on venous thromboembolism (VTE) risk. Search of PubMed, EMBASE, Web of Science, Scopus, ClinicalTrials.gov, LILACS, and Google Scholar databases to identify controlled observational and clinical trials reporting on adverse effects in patients treated with oral tofacitinib or baricitinib up to July 2020. The outcome measure was occurrence of VTE events. We analyzed 59 studies involving 14,335 patients treated with tofacitinib or baricitinib and 11,612 patients who received another active drug or placebo. The meta-analysis showed an odds ratio (OR) for VTE events of 0.29 (95% confidence interval [CI] = 0.10-0.84) overall for tofacitinib based on data from 10 clinical trials with 15 treatment arms; similar ORs were observed for the 10 mg/d dose (OR = 0.18; 95% CI = 0.02-1.60) and the 20 mg/d dose (OR = 0.19; 95% CI = 0.04-0.91). The ORs for VTE events for baricitinib were 3.39 (95% CI = 0.82-14.04) overall, 3.05 (95% CI = 0.12-75.43) for 2 mg, 3.64 (95% CI = 0.59-22.46) for 4 mg, and 3.0 (95% CI = 0.12-76.49) for 7 mg. The indirect meta-analysis comparing tofacitinib with baricitinib (10 clinical trials with 15 treatment arms) showed an OR for VTE events of 0.086 (95% CI = 0.02-0.51) for tofacitinib and a superior safety profile for VTE events. In the meta-regression analysis (19 clinical trials with 21 treatment arms), the effect was 0.02 (95% CI = -0.04 to 0.08) for tofacitinib and -0.01 (95% CI = -1.29 to 1.26 for baricitinib. Plotting of the data for tofacitinib showed that VTE risk increased with high doses. The effect, however, was less than 1 for the 10-mg and 20-mg doses, indicating a protective effect. This effect was not observed for baricitinib. Tofacitinib is not associated with an increased risk of VTE and has a superior safety profile to baricitinib in this respect. Tofacitinib may exert a protective effect against VTE.
© 2020 Pharmacotherapy Publications, Inc.

Entities:  

Keywords:  baricitinib; janus kinase inhibitors; thrombosis; tofacitinib; venous thromboembolism

Year:  2020        PMID: 33064892     DOI: 10.1002/phar.2472

Source DB:  PubMed          Journal:  Pharmacotherapy        ISSN: 0277-0008            Impact factor:   4.705


  6 in total

1.  Authors' Reply to Moura et al.: "Safety of Janus Kinase Inhibitors in Older Patients: A Focus on the Thromboembolic Risk".

Authors:  Suraj Rajasimhan; Omer Pamuk; James D Katz
Journal:  Drugs Aging       Date:  2021-04-19       Impact factor: 3.923

Review 2.  Thromboembolic Adverse Drug Reactions in Janus Kinase (JAK) Inhibitors: Does the Inhibitor Specificity Play a Role?

Authors:  Przemysław J Kotyla; Małgorzata Engelmann; Joanna Giemza-Stokłosa; Bartosz Wnuk; Md Asiful Islam
Journal:  Int J Mol Sci       Date:  2021-02-28       Impact factor: 5.923

Review 3.  Risk of venous thromboembolism associated with Janus kinase inhibitors for rheumatoid arthritis: case presentation and literature review.

Authors:  Shunsuke Mori; Fumihiko Ogata; Ryusuke Tsunoda
Journal:  Clin Rheumatol       Date:  2021-09-23       Impact factor: 2.980

Review 4.  Effect of Anti-Rheumatic Drugs on Cardiovascular Disease Events in Rheumatoid Arthritis.

Authors:  Yang Baoqi; Ma Dan; Zhao Xingxing; Zhu Xueqing; Wang Yajing; Xu Ke; Zhang Liyun
Journal:  Front Cardiovasc Med       Date:  2022-02-03

Review 5.  Tofacitinib and newer JAK inhibitors in inflammatory bowel disease-where we are and where we are going.

Authors:  Eleanor Liu; Nasar Aslam; Gaurav Nigam; Jimmy K Limdi
Journal:  Drugs Context       Date:  2022-04-08

6.  Oral Janus kinase inhibitors and venous thromboembolic events in atopic dermatitis: protocols for a case-time control study and a nested case-control study based on the French national health insurance (SNDS) cohort.

Authors:  Pauline Berthe; Lucie-Marie Scailteux; Alain Lescoat; Delphine Staumont; Guillaume Coiffier; Pierre Guéret; Alain Dupuy; Emmanuel Oger; Catherine Droitcourt
Journal:  BMJ Open       Date:  2022-09-21       Impact factor: 3.006

  6 in total

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