S1804 Comparing Infliximab and Adalimumab for Biomarker-Based Remission in Crohn’s Disease: Insights From Real-World Data

Introduction: Infliximab and adalimumab are cornerstone therapies for Crohn’s disease (CD), yet direct comparisons of their efficacy in achieving biomarker-based remission are limited. With the use of the TriNetX database, one of the largest and most diverse real-world cohorts to date, this study evaluates remission induction outcomes for these biologic agents, offering insights into their roles in CD management. Methods: We conducted a retrospective cohort study using TriNetX data from 93 healthcare organizations. A total of 16,291 adult patients (≥18 years) with CD treated with infliximab or adalimumab between 2018 and 2023 were initially identified. Propensity score matching was performed to balance age, sex, race/ethnicity, disease severity, and comorbidities, resulting in 6,516 matched CD patients per treatment group (total n = 13,032). The primary outcome was biomarker-based remission, defined as serum C-reactive protein (CRP) ≤5 mg/L or fecal calprotectin ≤150 µg/g, and assessed at 6 months, 1 year, 3 years, and 5 years. Induction of remission rates and Kaplan-Meier survival analyses were reported for the CD cohort. Results: Infliximab demonstrated consistently higher remission rates than adalimumab across all time points (P < 0.001). At 6 months, remission was achieved more frequently with Infliximab in CD (38.5% vs 28.3%). This pattern was held at 1 year (49.8% vs 42.6%), 3 years (66.1% vs 62.7%), and 5 years (71.2% vs 68.5%). Hazard ratios (HR) were directionally standardized to reflect infliximab over adalimumab (infliximab/adalimumab). Therefore, HR >1 indicates faster remission with infliximab. Infliximab was associated with a significantly shorter time to remission across all time points in CD (all HRs >1, P < 0.001). Median time to remission was also consistently shorter with infliximab compared to adalimumab across the CD group. This supports the hazard ratio findings and further shows a faster induction of remission with infliximab. Conclusion: Infliximab achieves more frequent and faster remission rates for CD at all time points. This may help guide biologic therapy selection and early treatment decisions in CD.

Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001134676.71438.91
Primary Topic
Inflammatory Bowel Disease
Type
article
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article

S1804 Comparing Infliximab and Adalimumab for Biomarker-Based Remission in Crohn’s Disease: Insights From Real-World Data

The American Journal of Gastroenterology
Inflammatory Bowel Disease
article

S1804 Comparing Infliximab and Adalimumab for Biomarker-Based Remission in Crohn’s Disease: Insights From Real-World Data

article en

Abstract

Introduction: Infliximab and adalimumab are cornerstone therapies for Crohn’s disease (CD), yet direct comparisons of their efficacy in achieving biomarker-based remission are limited. With the use of the TriNetX database, one of the largest and most diverse real-world cohorts to date, this study evaluates remission induction outcomes for these biologic agents, offering insights into their roles in CD management. Methods: We conducted a retrospective cohort study using TriNetX data from 93 healthcare organizations. A total of 16,291 adult patients (≥18 years) with CD treated with infliximab or adalimumab between 2018 and 2023 were initially identified. Propensity score matching was performed to balance age, sex, race/ethnicity, disease severity, and comorbidities, resulting in 6,516 matched CD patients per treatment group (total n = 13,032). The primary outcome was biomarker-based remission, defined as serum C-reactive protein (CRP) ≤5 mg/L or fecal calprotectin ≤150 µg/g, and assessed at 6 months, 1 year, 3 years, and 5 years. Induction of remission rates and Kaplan-Meier survival analyses were reported for the CD cohort. Results: Infliximab demonstrated consistently higher remission rates than adalimumab across all time points (P < 0.001). At 6 months, remission was achieved more frequently with Infliximab in CD (38.5% vs 28.3%). This pattern was held at 1 year (49.8% vs 42.6%), 3 years (66.1% vs 62.7%), and 5 years (71.2% vs 68.5%). Hazard ratios (HR) were directionally standardized to reflect infliximab over adalimumab (infliximab/adalimumab). Therefore, HR >1 indicates faster remission with infliximab. Infliximab was associated with a significantly shorter time to remission across all time points in CD (all HRs >1, P < 0.001). Median time to remission was also consistently shorter with infliximab compared to adalimumab across the CD group. This supports the hazard ratio findings and further shows a faster induction of remission with infliximab. Conclusion: Infliximab achieves more frequent and faster remission rates for CD at all time points. This may help guide biologic therapy selection and early treatment decisions in CD.

The American Journal of GastroenterologyVol. 120(10S2)
Good health and well-being
Openalex Percentile: Top 27%
Inflammatory Bowel Disease
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