Infliximab in young paediatric IBD patients: it is all about the dosing
Maria M E Jongsma1, Dwight A Winter1, Hien Q Huynh2
1Department of Paediatric Gastroenterology, Erasmus Medical Center/Sophia Children's Hospital, Rotterdam, The Netherlands.
Insights
Young children with inflammatory bowel disease (IBD) often have inadequate infliximab (IFX) levels. These young patients require a more intensive IFX treatment regimen to achieve therapeutic drug monitoring (TDM) levels and reduce antibody formation.
Area of Science:
- Pharmacokinetics and Pharmacodynamics
- Pediatric Gastroenterology
- Immunology
Background:
- Infliximab (IFX) is a critical biologic therapy for pediatric inflammatory bowel disease (PIBD).
- Current weight-based dosing may not optimize IFX exposure in younger children.
- Therapeutic drug monitoring (TDM) is essential for managing IFX therapy in PIBD.
Purpose of the Study:
- To assess IFX pharmacokinetics (PK) in PIBD patients under 10 years old.
- To compare IFX TDM data between young patients (YP, <10 years) and older patients (OP, 10-18 years).
- To determine if younger PIBD patients require a more intensive IFX treatment regimen.
Main Methods:
- Retrospective analysis of TDM data from 215 PIBD patients across 14 centers.
- Patients were stratified into YP (<10 years at IFX initiation) and OP (10-18 years).
- PK parameters, trough levels, required dosage adjustments, and antibody development were analyzed.
Main Results:
- 72% of YP had sub-therapeutic IFX trough levels at maintenance initiation.
- YP required significantly higher IFX doses (9.0 mg/kg) compared to OP (5.5 mg/kg) after one year (p < 0.001).
- YP had a higher likelihood of developing antibodies to infliximab compared to OP.
Conclusions:
- Younger PIBD patients (<10 years) often experience inadequate IFX exposure with standard dosing.
- An intensified induction regimen is recommended for PIBD patients under 10 years old.
- Optimizing IFX dosing in young children may improve treatment efficacy and reduce immunogenicity.
Abstract:
Infliximab (IFX) is administered intravenously using weight-based dosing (5 mg/kg) in inflammatory bowel disease (IBD) patients. Our hypothesis is that especially young children need a more intensive treatment regimen than the current weight-based dose administration. We aimed to assess IFX pharmacokinetics (PK), based on existing therapeutic drug monitoring (TDM) data in IBD patients < 10 years. TDM data were collected retrospectively in 14 centres. Children treated with IFX were included if IFX was started as IBD treatment at age < 10 years (young patients, YP) and PK data were available. Older IBD patients aged 10-18 years were used as controls (older patients, OP). Two hundred and fifteen paediatric inflammatory bowel disease (PIBD) patients were eligible for the study (110 < 10 year; 105 ≥ 10 years). Median age was 8.3 years (IQR 6.9-8.9) in YP compared with 14.3 years (IQR 12.8-15.6) in OP at the start of IFX. At the start of maintenance treatment, 72% of YP had trough levels below therapeutic range (< 5.4 μg/mL). After 1 year of scheduled IFX maintenance treatment, YP required a significantly higher dose per 8 weeks compared with OP (YP; 9.0 mg/kg (IQR 5.0-12.9) vs. OP; 5.5 mg/kg (IQR 5.0-9.3); p < 0.001). The chance to develop antibodies to infliximab was relatively lower in OP than YP (0.329 (95% CI - 1.2 to - 1.01); p < 0.001), while the overall duration of response to IFX was not significantly different (after 2 years 53% (n = 29) in YP vs. 58% (n = 45) in OP; p = 0.56).Conclusion: Intensification of the induction scheme is suggested for PIBD patients aged < 10 years. What is Known? •Infliximab trough levels of paediatric IBD patients are influenced by several factors as dosing scheme, antibodies and inflammatory markers. •In 4.5-30% of the paediatric IBD patients, infliximab treatment was stopped within the first year. What is New? •The majority of young PIBD (< 10 years) have inadequate IFX trough levels at the start of maintenance treatment. •Young PIBD patients (< 10 years) were in need of a more intensive treatment regimen compared with older paediatric patients during 1 year of IFX treatment. •The chance to develop antibodies to infliximab was relatively higher in young PIBD patients (< 10 years).
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