Abstract

Biologicals are very effective for inhibiting disease progression in active juvenile idiopathic arthritis (JIA). To date, there have been no recommendations on how and when to stop therapy with TNF inhibitors. Our objective was to analyze characteristics and the disease course of JIA patients who discontinued etanercept due to achievement of inactive disease. Data of 39 patients with JIA from two clinical pediatric rheumatology centers in Bydgoszcz and Lublin (Poland) were analyzed retrospectively. All patients discontinued etanercept due to a remission on treatment. Etanercept was started after a mean 33.7 ± 36 (range 3–137) months of disease. The mean duration of therapy with etanercept was 34.7 ± 16.7 (range 6–72) months, with a mean duration of remission on medication 21.3 ± 9.6 (range 4–42) months before withdrawal of etanercept. The mean duration of remission after etanercept discontinuation was 14.2 ± 12.1 (range of 1–60) months. Only 12/39 (30.8 %) patients did not develop a disease exacerbation until the end of the study. Early flares, that is less than 6 months after termination of etanercept, were observed in 15/39 (38.5 %) patients. Twelve (30.8 %) patients restarted etanercept after exacerbation—all patients responded satisfactorily. Our data show that etanercept discontinuation in a substantial proportion of JIA patients results in early disease exacerbation. In many cases, reintroduction of etanercept is needed. Patients, in whom etanercept was restarted, responded satisfactorily.

Highlights

  • Biologicals are very effective for inhibiting disease progression in active juvenile idiopathic arthritis (JIA)

  • That is less than 6 months after termination of etanercept, were observed in 15/39 (38.5 %) patients

  • Our data show that etanercept discontinuation in a substantial proportion of JIA patients results in early disease exacerbation

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Summary

Introduction

Biologicals are very effective for inhibiting disease progression in active juvenile idiopathic arthritis (JIA). Our objective was to analyze characteristics and the disease course of JIA patients who discontinued etanercept due to achievement of inactive disease. Data of 39 patients with JIA from two clinical pediatric rheumatology centers in Bydgoszcz and Lublin (Poland) were analyzed retrospectively. All patients discontinued etanercept due to a remission on treatment. Etanercept was started after a mean 33.7 ± 36 (range 3–137) months of disease. The mean duration of remission after etanercept discontinuation was 14.2 ± 12.1 (range of 1–60) months. Opoka-Winiarska Department of Pediatric Lung Diseases and Rheumatology, Medical University of Lublin, Lublin, Poland. Our data show that etanercept discontinuation in a substantial proportion of JIA patients results in early disease exacerbation. In whom etanercept was restarted, responded satisfactorily. In spite of treatment applied, in some patients, disease activity is continued into adulthood [1, 2]

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