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Real-world effectiveness of tofacitinib in patients with rheumatoid arthritis: a prospective observational study

Authors :
Aniela, Shouval
Merav, Lidar
Tatiana, Reitblat
Devy, Zisman
Alexandra, Balbir-Gurman
Tanya, Mashiach
Ronit, Almog
Ori, Elkayam
Source :
Clinical and Experimental Rheumatology. 39:1378-1384
Publication Year :
2021
Publisher :
Clinical and Experimental Rheumatology, 2021.

Abstract

Tofacitinib is an approved treatment for rheumatoid arthritis (RA), but data on its use in the "real-world" are limited. We sought to analyse tofacitinib drug survival in the Israeli registry and compare it to other biologic agents.We included RA patients treated with tofacitinib, etanercept, golimumab, tocilizumab, or abatacept between 2010-2019. The primary endpoint was event-free survival (EFS), defined as the time from treatment initiation to a treatment failure event from any cause (i.e., inefficacy or intolerability). EFS was compared between agents using Cox regression and Kaplan-Meier analysis, stratifying patients by treatment line.A total of 964 eligible treatment courses were included (tocilizumab [325], etanercept [284], abatacept [127], tofacitinib [139], and golimumab [109]). In a univariate analysis, EFS with tofacitinib in the complete cohort was similar to etanercept, golimumab, and abatacept but was lower than tocilizumab) 3-year EFS 43% vs. 53%, HR 0.65). In a multivariable analysis, tofacitinib was similar to all other drugs, except for etanercept, which was inferior (HR 1.70); advanced treatment line was also associated with greater risk for failure (HR 1.64). In a univariable analysis stratified by the treatment line, tofacitinib had similar or better drug survival than other agents in the first and second lines. In the third line and beyond, tocilizumab had a higher EFS compared to tofacitinib (HR 0.57).Drug survival with tofacitinib is related to treatment line. Early introduction is associated with similar or better survival than other agents, whereas tocilizumab was superior in the third line or later.

Details

ISSN :
1593098X and 0392856X
Volume :
39
Database :
OpenAIRE
Journal :
Clinical and Experimental Rheumatology
Accession number :
edsair.doi.dedup.....36885df96dfd06dffd2a329e0bd85a02