The purpose of this study is to determine whether etanercept can be withdrawn successfully (i.e. no occurrence of flares) in juvenile idiopathic arthritis (JIA) patients in whom disease remission is reached. Goals: 1. to investigate in a randomized controlled trial: * which proportion of JIA patients in remission can successfully discontinue etanercept compared to JIA patients in remission who continue etanercept; * if time in remission on etanercept is an important factor in retaining remission after discontinuation of etanercept. 2. to investigate in alle JIA patients who discontinue etanercept (including the control group): * predicting factors (patient or disease characteristics, including time in remission, and MRP8/MRP14) for successfully discontinuation of etanercept; * the disease course after discontinuation of etanercept (time to flare) and the effect of restarting etanercept after flaring.
Juvenile Idiopathic Arthritis (JIA) is the most common cause of chronic arthritis in children. Etanercept has proven to be an effective treatment for JIA. Considering the risk of occurrence of long-term side-effects and to prevent the burden of the weekly injections and costs, it is a logical step to discontinue etanercept after reaching remission (no disease activity for at least six months). Especially since there are concerns about the long-term effect of suppressing the immune system with etanercept. However, little is known about if successful discontinuation is possible or when to stop. Risk is that the disease might flare (reactivate) again. For this study, JIA patients in remission will be selected from the ABC-register (an observational study including all Dutch JIA patients who use etanercept). Eligible patients will be randomized to stop etanercept or continue it for another 9 months. Patients are followed with standard visits evaluating disease activity until 12 months after discontinuation of etanercept. In case of a disease flare etanercept therapy will be reintroduced immediately and the patient will be treated according to the insight of their treating physician. Expected is that JIA patients who were in remission for more than 12 months before discontinuation have a better chance to retain remission.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
50
Discontinuation of etanercept (half of the dosis for 3 months and discontinuation thereafter)
Continuation of etanercept for another 9 months, and, if still meeting the eligibility criteria, discontinuation of etanercept thereafter.
Academic Medical Centre Emma Children's Hospital
Amsterdam, Netherlands
NOT_YET_RECRUITINGReade Institute Amsterdam
Amsterdam, Netherlands
NOT_YET_RECRUITINGSint-Lucas Andreas Hospital
Amsterdam, Netherlands
ACTIVE_NOT_RECRUITINGUniversity Medical Centre Groningen
Groningen, Netherlands
NOT_YET_RECRUITINGLeiden University Medical Center
Leiden, Netherlands
NOT_YET_RECRUITINGMaastricht University Medical Centre
Maastricht, Netherlands
NOT_YET_RECRUITINGSt Maartenskliniek
Nijmegen, Netherlands
NOT_YET_RECRUITINGErasmus MC Sophia Children's Hospital
Rotterdam, Netherlands
RECRUITINGHaga Hospital, Juliana Children's Hospital
The Hague, Netherlands
NOT_YET_RECRUITINGUtrecht Medical Centre Wilhelmina Children's Hospital
Utrecht, Netherlands
NOT_YET_RECRUITINGFlare-rate
To evaluate if the flare-rate is different between the 2 arms (continuation and discontinuation of etanercept).
Time frame: 9 months
Duration of remission before withdrawal of etanercept
To evaluate between the 2 arms (continuation and discontinuation of etanercept) if time in remission on etanercept is an important factor in retaining remission after discontinuation of etanercept.
Time frame: 9 months
Predictors for successful discontinuation of etanercept
Evaluation of predictors (patient or disease characteristics, including time in remission, and MRP8/MRP14) for successful discontinuation of etanercept in all JIA patient who discontinue etanercept.
Time frame: 12 months after discontinuation of etanercept
Disease course after flaring
After a flare (exacerbation) occurs: evaluation of time to flare and the effect of restarting etanercept after flaring.
Time frame: 6 months after flare
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