When and how to stop etanercept after successful treatment of patients with juvenile idiopathic arthritis
1 Department of Paediatrics/Paediatric Rheumatology, Erasmus MC Sophia Childrens Hospital, Rotterdam, The Netherlands
2 Department of Paediatrics/Paediatric Rheumatology, Leiden University Medical Centre, The Netherlands
3 Department of Paediatrics/Paediatric Rheumatology, Emma Childrens Hospital AMC and Jan van Breemen Institute, Amsterdam, The Netherlands
4 Department of Paediatrics/Paediatric Rheumatology, Beatrix Childrens Hospital, University Medical Centre Groningen, The Netherlands
5 Department of Paediatrics/Paediatric Rheumatology, University Nijmegen Medical Centre Radboud, The Netherlands
6 Department of Internal Medicine, subdivision Rheumatology, Maastricht University Medical Centre, The Netherlands
7 Department of Paediatrics, Hagaziekenhuis Juliana Childrens Hospital, Den Haag, The Netherlands
8 Department of Paediatrics/Paediatric Rheumatology, Utrecht MC Wilhelmina Childrens Hospital, The Netherlands
Correspondence to:
F H M Prince, Department of Paediatrics, Sp 1546, Erasmus MC Sophia Childrens Hospital, PO Box 2060, 3000 CB Rotterdam, The Netherlands; f.prince@erasmusmc.nl
Accepted 22 September 2008
| The first 150 words of the full text of this article appear below. |
Currently, little is known about when or how to stop etanercept in patients with juvenile idiopathic arthritis (JIA) when a good clinical response is reached, and therefore no guidelines are available.1 We evaluated the disease course of patients with JIA who discontinued etanercept because of a sustained good clinical response.
This study is embedded in the Arthritis and Biologicals in Children (ABC) project, a prospective ongoing multicentre, observational study that includes all Dutch patients with JIA who used etanercept since 1999.2 3 We selected all patients who discontinued etanercept because of sustained good clinical response determined by the treating doctor. The outcome measures to assess disease activity consisted of the JIA core set of six response variables.4 To evaluate the disease course we used the criteria for inactive disease on medication (IDM) or off medication (ID) and the criteria for clinical remission on medication (CRM) or off medication (CR) by Wallace.5 6
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