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Clinical remission in juvenile idiopathic arthritis after termination of etanercept
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 di...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3782656/ https://www.ncbi.nlm.nih.gov/pubmed/22821261 http://dx.doi.org/10.1007/s00296-012-2468-3 |
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author | Postępski, Jacek Kobusińska, Katarzyna Olesińska, Edyta Osińska, Violetta Opoka-Winiarska, Violetta |
author_facet | Postępski, Jacek Kobusińska, Katarzyna Olesińska, Edyta Osińska, Violetta Opoka-Winiarska, Violetta |
author_sort | Postępski, Jacek |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-3782656 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-37826562013-09-25 Clinical remission in juvenile idiopathic arthritis after termination of etanercept Postępski, Jacek Kobusińska, Katarzyna Olesińska, Edyta Osińska, Violetta Opoka-Winiarska, Violetta Rheumatol Int Short Communication 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. Springer Berlin Heidelberg 2012-07-21 2013 /pmc/articles/PMC3782656/ /pubmed/22821261 http://dx.doi.org/10.1007/s00296-012-2468-3 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Short Communication Postępski, Jacek Kobusińska, Katarzyna Olesińska, Edyta Osińska, Violetta Opoka-Winiarska, Violetta Clinical remission in juvenile idiopathic arthritis after termination of etanercept |
title | Clinical remission in juvenile idiopathic arthritis after termination of etanercept |
title_full | Clinical remission in juvenile idiopathic arthritis after termination of etanercept |
title_fullStr | Clinical remission in juvenile idiopathic arthritis after termination of etanercept |
title_full_unstemmed | Clinical remission in juvenile idiopathic arthritis after termination of etanercept |
title_short | Clinical remission in juvenile idiopathic arthritis after termination of etanercept |
title_sort | clinical remission in juvenile idiopathic arthritis after termination of etanercept |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3782656/ https://www.ncbi.nlm.nih.gov/pubmed/22821261 http://dx.doi.org/10.1007/s00296-012-2468-3 |
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