Intravenous Versus Subcutaneous Infliximab in Inflammatory Bowel Disease: A Systematic Review and Meta-analysis.
John David Chetwood1,2, Yvonne Tran3, Sreedhar Subramanian4
1Department of Gastroenterology and Hepatology, Concord Repatriation General Hospital, Sydney, NSW, Australia.
Switching to subcutaneous infliximab maintains clinical remission in inflammatory bowel disease (IBD) patients. This transition is safe across IBD subtypes and different prior intravenous dosing, supporting its use.
Area of Science:
- Gastroenterology and Immunology
- Pharmacology and Therapeutics
Background:
- Subcutaneous (SC) infliximab offers potential advantages over intravenous (IV) formulations for inflammatory bowel disease (IBD) management.
- Previous studies on SC infliximab efficacy and safety in IBD were limited by small sample sizes, hindering subgroup analysis, especially for high-risk patients.
Approach:
- A systematic review and random-effects meta-analysis was performed, analyzing data up to January 2023.
- The study evaluated the change in clinical remission rates after transitioning IBD patients from IV to SC infliximab.
- Relative risk was used as the primary outcome measure to assess remission maintenance.
Key Points:
- Analysis included 15 studies with 1371 patients established on IV infliximab for at least 3 months.
- No significant loss of clinical remission was observed overall, in Crohn's disease (CD), or perianal CD patients.
- Neither prior IV dose escalation (≤10 mg/kg 6-weekly) nor IBD disease subtype (UC vs. CD) correlated with increased relapse rates at 6 months.
Conclusions:
- Transitioning from IV to SC infliximab in IBD patients demonstrates sustained clinical remission and a low adverse event profile.
- No increased risk of adverse outcomes was identified in specific IBD subtypes or in patients previously on escalated IV infliximab doses.
- These findings support the confidence of patients and clinicians in utilizing SC infliximab for IBD treatment.
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