Tofacitinib: Real-World Data and Treatment Persistence in Rheumatoid Arthritis.

IF 1.7 Q3 RHEUMATOLOGY
Open Access Rheumatology-Research and Reviews Pub Date : 2021-07-27 eCollection Date: 2021-01-01 DOI:10.2147/OARRR.S322086
Ilaria Bertoldi, Roberto Caporali
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引用次数: 0

Abstract

Tofacitinib is an oral Janus kinase (JAK) inhibitor indicated for the treatment of rheumatoid arthritis (RA). The efficacy and safety/tolerability of tofacitinib have been extensively evaluated as monotherapy and combination therapy in multiple, randomised, multicentre studies in patients with RA. Tofacitinib as monotherapy (as first- and second-line treatment) or as combination with methotrexate (MTX) or other csDMARDs as second- and third-line treatment is effective and generally well tolerated in patients with RA. This article focuses on recent real-world evidence investigating the effectiveness, treatment persistence and safety/tolerability of tofacitinib in patients with RA. With this purpose, a literature review was conducted from April 2018 up to October 2020 for the effectiveness, persistence and safety of tofacitinib for the treatment of RA, primarily focusing on real-world studies. These retrospective and prospective and observational studies demonstrate the effectiveness of tofacitinib, thus supporting pivotal data from the clinical trial programme. Treatment persistence was generally comparable to that of biologic disease-modifying anti-rheumatic drugs. Safety findings in these observational studies were consistent with the known safety profile of the approved dose of 5 mg twice daily.

托法替尼类风湿关节炎的真实世界数据和治疗持续性。
托法替尼是一种口服 Janus 激酶(JAK)抑制剂,适用于治疗类风湿性关节炎(RA)。多项针对 RA 患者的随机多中心研究对托法替尼作为单一疗法和联合疗法的疗效和安全性/耐受性进行了广泛评估。托法替尼作为单药治疗(一线和二线治疗)或与甲氨蝶呤(MTX)或其他csDMARDs联用作为二线和三线治疗对RA患者有效且耐受性良好。本文重点介绍了近期调查托法替尼在RA患者中的有效性、治疗持续性和安全性/耐受性的实际证据。为此,我们对2018年4月至2020年10月期间有关托法替尼治疗RA的有效性、持续性和安全性的文献进行了回顾,主要侧重于真实世界研究。这些回顾性、前瞻性和观察性研究证明了托法替尼的有效性,从而为临床试验计划的关键数据提供了支持。治疗的持续性一般与生物制剂改变病情抗风湿药物相当。这些观察性研究的安全性结果与获批剂量(5 毫克,每日两次)的已知安全性特征一致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.80
自引率
0.00%
发文量
34
审稿时长
16 weeks
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