Abstract

BackgroundTreat-to-target (T2T) is a widely accepted strategy for patients with rheumatoid arthritis (RA). It recommends attaining a goal of at least low disease activity (LDA) within 6 months; otherwise, the current therapy should be modified. We aimed to investigate whether switching a first-line targeted therapy (TT) in patients not reaching LDA within 6 months leads to a higher probability of meeting LDA at the 12-month visit in daily clinical practice using data from Czech registry ATTRA.MethodsWe included patients with RA starting the first-line TT from 1 January 2012 to 31 January 2017 with at least 1-year follow-up. We created four mutually exclusive cohorts based on (1) switching to another TT within the first year and (2) reaching a treatment target (DAS28-ESR ≤ 3.2) at the 6-month visit. The primary outcome was the comparison of odds for reaching remission (REM) or LDA at the 12-month visit between patients switching and not switching TT after not reaching treatment target at 6 months. Before using logistic regression to estimate the odds ratio, we employed the propensity score to match patients at the 6-month visit.ResultsA total of 1275 patients were eligible for the analysis. Sixty-two patients switched within the first 5 months of the treatment before evaluating treatment response at the 6-month visit (C1); 598 patients reached the treatment target within 6 months of therapy (C2); 124 patients did not reach treatment response at 6-month visit and switched to another therapy (C3), and 491 patients continued with the same treatment despite not reaching LDA at the 6-month visit (C4). We matched 75 patients from cohort C3 and 75 patients from C4 using the propensity score. Patients following the T2T principle (C3) showed 2.8 (95% CI 1.4–5.8; p = 0.005) times increased likelihood of achieving REM/LDA at the 12-month visit compared to patients not following the T2T strategy (C4).ConclusionsIn daily clinical practice, the application of the T2T strategy is underused. Switching TT after not reaching REM/LDA within the first 6 months leads to a higher probability of achieving REM/LDA in RA patients at the 12-month visit.

Highlights

  • Treat-to-target (T2T) is a widely accepted strategy for patients with rheumatoid arthritis (RA)

  • Switching targeted therapy (TT) after not reaching REM/low disease activity (LDA) within the first 6 months leads to a higher probability of achieving REM/LDA in RA patients at the 12-month visit

  • Patients with RA starting Biological diseasemodifying anti-rheumatic drugs (bDMARDs) or tsDMARDs are recruited from fifty practice sites, which captures more than 95% of patients with RA treated with bDMARDs/ tsDMARDs in the Czech Republic (CZ)

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Summary

Introduction

Treat-to-target (T2T) is a widely accepted strategy for patients with rheumatoid arthritis (RA). It recommends attaining a goal of at least low disease activity (LDA) within 6 months; otherwise, the current therapy should be modified. In 2010, the European League Against Rheumatism (EULAR) developed its first recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs (DMARDs) [1]. If the treatment target is not reached with the first csDMARDs, and poor prognostic factors are present (i.e. presence of rheumatoid factor/anti-citrullinated protein antibodies, high disease activity early, joint damage, failure of two or more csDMARDs), a biological (b) DMAR D or targeted synthetic (ts) DMARD should be added. If there is no improvement within 3 months after the start of treatment or if patients have not reached the treatment target with bDMARD/tsDMARD by 6 months, therapy should be adjusted, and treatment with another bDMARD or tsDMARD should be considered [2]

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