Abstract

BackgroundEarly and intensive targeted treatment with disease modifying anti-rheumatic drugs (DMARDs) has been shown to lead to substantial reductions in disease activity and radiograph damage in patients with early rheumatoid arthritis (RA). The aim of this quasi-experimental study was to compare the first-year radiographic progression rates between a treat-to-target (T2 T) strategy with initial combination therapy (strategy II, started in 2012) versus an initial step-up monotherapy (strategy I, started in 2006).MethodsA total of 128 patients from strategy II was individually matched with 128 patients from strategy I on sex, age (± 5 yrs.) and baseline disease activity (± 0.5 on the DAS28). Differences in radiographic progression (Sharp/van der Heijde) scores (SHS) and the number of patients experiencing a minimal clinically important difference (MCID; ≥ 5 SHS points) between both strategies were tested with Mann Whitney U and chi-square tests. Next, linear and logistic regression analyses were performed to examine which baseline variables were associated with radiographic progression scores and the probability of experiencing an MCID within 1 year.ResultsPatients with initial combination therapy had slightly higher baseline disease activity scores and pain scores, but better mental health scores. Patients with initial monotherapy had significantly more, and more frequently clinically relevant, radiographic progression after 1 year. Experiencing a MCID was independently associated with fewer tender joints (p = 0.050) and higher erythrocyte sedimentation rate (p = 0.015) at baseline.ConclusionTreating early RA patients with initial combination therapy results in better radiographic outcomes than initial monotherapy in daily clinical practice.Trial registrationNetherlands Trial Register NTR578, 12 January 2006.

Highlights

  • And intensive targeted treatment with disease modifying anti-rheumatic drugs (DMARDs) has been shown to lead to substantial reductions in disease activity and radiograph damage in patients with early rheumatoid arthritis (RA)

  • The benefits of early use of disease modifying anti-rheumatic drugs (DMARDs) and biological agents [7,8,9,10,11,12], in combination with protocolled treatment aimed at a predefined goal (treat-to-target (T2T)) [13,14,15], has led to a change in traditional treatment paradigms

  • Early and intensive targeted treatment with DMARDs has been shown to lead to substantial reductions in disease activity [5, 6] and radiologic damage in patients with early RA [8, 13, 16,17,18,19,20,21]

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Summary

Introduction

And intensive targeted treatment with disease modifying anti-rheumatic drugs (DMARDs) has been shown to lead to substantial reductions in disease activity and radiograph damage in patients with early rheumatoid arthritis (RA). The aim of this quasi-experimental study was to compare the first-year radiographic progression rates between a treat-to-target (T2 T) strategy with initial combination therapy (strategy II, started in 2012) versus an initial step-up monotherapy (strategy I, started in 2006). Whether the complete absence of arthritis activity prevents further joint damage in all patients, is still a matter of debate

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