Anti-TNF treatment (infliximab (IFX), adalimumab (ADA)) has become standard therapy for refractory pediatric and adult Crohn¡¯s disease (CD) patients, and is used for the induction and maintenance of remission. When effective, clinical and…
ID
Bron
Verkorte titel
Aandoening
Inflammatory Bowel Disease, pediatric, anti-TNF therapy, IBD
Kinderen, chronische darmziekten
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Clinical efficacy of IFX treatment in pediatric IBD patients (¡Ü 9 years) in relation to<br>
- Antropometric data<br>
- Clinical data<br>
- Pharmacokinetics (including the presence of antibodies to IFX)<br>
- Safety<br>
o Number of (serious) adverse events
Doel van het onderzoek
Anti-TNF treatment (infliximab (IFX), adalimumab (ADA)) has become standard therapy for refractory pediatric and adult Crohn¡¯s disease (CD) patients, and is used for the induction and maintenance of remission. When effective, clinical and endoscopic remission is reached within weeks. In ulcerative colitis anti-TNF treatment is also increasingly used, and has been shown to induce remission in active disease.
Early IFX pharmacokinetic (PK) data showed a consistent trend towards lower mean serum IFX concentrations after a single dose of 5 and 10 mg/kg in pediatric compared to adult CD patients. Over time some papers have suggested IFX PK are not statistically different between pediatric and adult CD or UC patients. However recent data suggests decreased sustained IFX efficacy in early-onset IBD patients (< 8 years), specifically in children 5 years old and younger.
Alternate absorption, distribution, metabolism and excretion between children and adults may all play a role.(Shi and Derendorf 2010). The exact underlying mechanisms are currently incompletely understood. Our primary aim is to assess pharmacokinetics of IFX, based on existing therapeutic drug monitoring (TDM) data, in relation to efficacy and safety in pediatric IBD patients below the age of 9 years. Our secondary aim is to construct a dosing guideline based on these retrospectively collected data for more accurate IFX dosing.
Onderzoeksopzet
Not Applicable
Onderzoeksproduct en/of interventie
Retrospective collection of data
Publiek
Wetenschappelijk
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
Pediatric IBD patients (¡Ü 9 years) who have initiated IFX treatment because
of active luminal disease, failing treatment with immunomodulators and
corticosteroids
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
- IFX treatment started for a condition other than IBD
- Missing data on IFX dosing or levels
- Age > 9 years when IFX treatment was initiated
Opzet
Deelname
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Register | ID |
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NTR-new | NL5390 |
NTR-old | NTR5491 |
Ander register | Erasmus MC Rotterdam : MEC-2015-503 |