Abstract

Tumor necrosis factor inhibitors (TNFi) are widely used for the treatment of patients with rheumatoid arthritis (RA), however a considerable percentage of patients discontinued the therapy. The aim of this study is to explore real-world TNFi survival, stratified for seropositivity, and to determine the factors that may influence it. This is a retrospective, observational and longitudinal study, using real-world data of patients, who started their first TNFi therapy between 1999 and 2018 from the RA-PAZ cohort. Patients were considered seropositive if they showed positive serum levels of either RF, ACPA, or both. Treatment survival was analyzed using Kaplan-Meier curves, and Cox proportional hazards models were used to compare the risks of TNFi discontinuation for seronegative and seropositive patients. Of the included 250 patients, 213 (85%) were seropositive. Results showed that TNFi survival did not depend on seropositivity status. However, median survival time was significant longer for seropositive patients who received concomitant MTX compared to patients who did not receive it (median [95% CI]: 3.3 yr. [2.3–4.2] vs. 2.6 yr. [1.7–3.6], respectively; p = 0.008). Furthermore, seropositive patients who received concomitant MTX were 49% less likely to discontinue TNFi therapy than patients who did not receive it (HR: 0.51; 95% CI: 0.35–0.74). In addition, we found that in seropositive patients, the use of prednisone throughout the TNFi treatment was associated with a higher likelihood of therapy discontinuation (OR: 2.30; 95% CI: 1.01–5.23). In conclusion, these data provide evidence to support the use of concomitant MTX in seropositive patients to prolong the effectiveness and the survival of the TNFi therapy. Moreover, the co-administration of prednisone in seropositive patients receiving TNFi was highly associated with TNFi discontinuation.

Highlights

  • Tumor necrosis factor inhibitors (TNFi) are widely used for the treatment of patients with rheumatoid arthritis (RA), who do not respond to conventional synthetic disease-modifying antirheumatic drugs

  • After the univariable logistic regression analyses, we found that the use of prednisone throughout the TNFi treatment (OR: 2.29; 95% confidence interval (CI): 1.11–4.71) was significant associated with TNFi discontinuation

  • We found that the use of prednisone throughout the TNFi treatment (OR: 2.46; 95% CI: 1.10–5.51) was significant associated with TNFi discontinuation only in seropositive patients

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Summary

Introduction

Tumor necrosis factor inhibitors (TNFi) are widely used for the treatment of patients with rheumatoid arthritis (RA), who do not respond to conventional synthetic disease-modifying antirheumatic drugs (csDMARDs). Serum autoantibodies have been correlated with a higher disease activity [5, 6], which has been associated with an increase of TNFi clearance due to the inflammatory sink that would lead to an early drug administration stopping [7, 8]. In this line, some studies have pointed out that the autoantibody seropositive status, mainly due to RF or ACPA, may be influencing the survival of TNFi as well as blood TNFi levels [9, 10]. Blood concentrations are higher for patients with RA treated with TNFi when MTX is co-prescribed from the start of treatment [11,12,13], and it is already recommended by the European Alliance of Associations for Rheumatology (EULAR) [14]

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