Evaluation of Infliximab Therapy in Children with Crohn's Disease Using Trough Levels Predictors
Jan Ohem1, Ondrej Hradsky, Kristyna Zarubova
1Gastroenterology and Nutrition Unit, Department of Paediatrics, 2nd Faculty of Medicine, Charles, University and Motol University Hospital, Prague, Czech Republic.
Insights
Infliximab (IFX) levels in children with Crohn's disease correlate with disease activity and antibodies to IFX (ATIs). Lower IFX levels are linked to ATIs and higher inflammatory markers, similar to adults.
Area of Science:
- Pediatric Gastroenterology
- Immunology
- Pharmacokinetics
Background:
- Infliximab (IFX) levels and antibodies to IFX (ATIs) impact treatment outcomes in adult Crohn's disease (CD).
- Understanding these associations in pediatric CD is crucial for optimizing therapy.
Purpose of the Study:
- To investigate the relationship between IFX levels, ATIs, and disease activity in pediatric CD patients.
- To identify predictors of IFX levels during maintenance therapy.
Main Methods:
- Prospective study of 65 pediatric CD patients (age 10.5-15.1 years) receiving IFX maintenance therapy.
- Measurement of IFX trough levels, ATIs, fecal calprotectin (CPT), CRP, and ESR.
- Multivariate analysis to determine predictors of IFX levels and associations with disease activity.
Main Results:
- Lower IFX levels were associated with ATI positivity (OR 0.027).
- Higher CRP, ESR, and CPT levels correlated with lower IFX levels.
- Optimal IFX trough levels for remission were identified as ≥1.1 µg/mL (with CRP <5 mg/L) or 3.5 µg/mL (with CPT ≤100 µg/g).
- An independent association was found between IFX levels and serum albumin (OR 1.364).
Conclusions:
- Pediatric CD patients exhibit similar associations between IFX levels, ATIs, and disease activity as adults.
- Therapeutic drug monitoring of IFX may be beneficial in pediatric CD.
- Serum albumin levels are independently associated with IFX levels in this population.
Background:
In adults, infliximab (IFX) levels correlate with disease activity, and antibodies to IFX (ATIs) predict treatment failure. We aimed to determine the association of IFX levels and ATIs with disease activity in a paediatric population. We prospectively collected blood, stool, and clinical data from 65 patients (age 10.5-15.1 years) with Crohn's disease (CD) before IFX administration, and measured IFX trough levels, ATIs, and faecal calprotectin levels (CPT). Samples were collected during maintenance therapy. We used multivariate analysis to identify the predictors of IFX levels.
Summary:
Lower levels of IFX were associated with ATIs positivity (OR 0.027, 95% CI 0.009-0.077). Higher C-reactive protein (CRP) level, erythrocyte sedimentation rate, and CPT levels were found in patients with lower IFX levels. The optimal combination of sensitivity (0.5) and specificity (0.74) for disease activity was calculated for IFX levels ≥1.1 µg/mL using CRP level <5 mg/L as a marker of laboratory remission. In a model that used CPT ≤100 µg/g as the definition of remission, the optimal IFX trough level was 3.5 µg/mL. No independent association between remission and ATIs was found in our study population. However, we found an independentz association between IFX levels and serum albumin levels (OR 1.364, 95% CI 1.169-1.593), p < 0.001. Key Messages: The paediatric population was similar to adult populations in terms of the association between IFX and ATIs as well as between IFX and disease activity.
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