Adalimumab vs Infliximab in Luminal Pediatric Crohn's Disease: Comparable Outcomes in a Prospective Multicenter
Jennifer C deBruyn1, Hien Q Huynh2, Anne M Griffiths3,4
1Alberta Children's Hospital, University of Calgary, Calgary, Alberta, Canada.
Insights
In pediatric Crohn's disease (CD), both adalimumab (ADA) and infliximab (IFX) as first anti-tumor necrosis factor (anti-TNF) therapies yield comparable outcomes at one year. Treatment intensification was less frequent with ADA compared to IFX.
Area of Science:
- Pediatric Gastroenterology
- Immunology
- Clinical Therapeutics
Background:
- Crohn's disease (CD) is a chronic inflammatory condition affecting children.
- Anti-tumor necrosis factor (anti-TNF) agents like adalimumab (ADA) and infliximab (IFX) are crucial for managing pediatric CD.
- Real-world effectiveness data comparing ADA and IFX as initial anti-TNF therapy in children is essential.
Purpose of the Study:
- To compare the real-world effectiveness of adalimumab (ADA) versus infliximab (IFX) as the first anti-TNF agent in children with Crohn's disease (CD).
- To evaluate outcomes including clinical remission, combined remission, treatment intensification, and anti-TNF durability at one year.
Main Methods:
- A prospective cohort study of children with luminal CD initiating ADA or IFX as their first anti-TNF agent.
- Propensity score matching was employed to create comparable groups of ADA- and IFX-treated children.
- Outcomes assessed at one year included steroid-free clinical remission (SFCR), combined SFCR and C-reactive protein remission, treatment intensification, and anti-TNF durability.
Main Results:
- In the matched cohort (147 ADA, 147 IFX), SFCR at one year was achieved by 63% of ADA-treated and 59% of IFX-treated children (aOR 1.4).
- Combined SFCR and C-reactive protein remission was similar between groups (54% ADA vs. 59% IFX; aOR 1.0).
- Treatment intensification was significantly lower in the ADA group (14%) compared to the IFX group (47%) (P < 0.0001). Anti-TNF discontinuation rates were similar.
Conclusions:
- Both adalimumab and infliximab demonstrate favorable one-year outcomes when used as first-line anti-TNF therapy in pediatric Crohn's disease.
- While clinical remission rates were comparable, adalimumab was associated with less frequent treatment intensification compared to infliximab.
Introduction:
This study compared real-world effectiveness between adalimumab (ADA) and infliximab (IFX) in children with Crohn's disease (CD).
Methods:
Children enrolled into the prospective Canadian Children Inflammatory Bowel Disease Network National Inception Cohort between 2014 and 2020 who commenced ADA or IFX as first antitumor necrosis factor (anti-TNF) agent for luminal CD were included. Multivariate logistic regression modeled the propensity of commencing ADA; propensity score matching was used to match IFX-treated children to ADA-treated children. The primary outcome at 1 year was steroid-free clinical remission (SFCR). Secondary outcomes at 1 year were (i) combined SFCR and C-reactive protein remission, (ii) treatment intensification, and (iii) anti-TNF durability. Odds ratios (ORs) and hazard ratio adjusted for concomitant immunomodulator use with 95% confidence interval (CI) are reported.
Results:
In the propensity score-matched cohort of 147 ADA-treated and 147 IFX-treated children, 92 (63%) ADA-treated and 87 (59%) IFX-treated children achieved SFCR at 1 year (adjusted OR 1.4, 95% CI 0.9-2.4); 75 of 140 (54%) ADA-treated and 85 of 144 (59%) IFX-treated children achieved combined SFCR and C-reactive protein remission (adjusted OR 1.0, 95% CI 0.6-1.6). ADA-treated children less frequently underwent treatment intensification (21 [14%]) compared with IFX-treated children (69 [47%]) ( P < 0.0001). Discontinuation of anti-TNF occurred in 18 (12%) ADA-treated and 15 (10%) IFX-treated children (adjusted hazard ratio 1.2, 95% CI 0.6-2.2).
Discussion:
Children with CD achieved favorable outcomes at 1 year with either ADA or IFX as first anti-TNF agents. Those receiving IFX did not have significantly superior outcomes compared with clinically similar children receiving ADA.
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