S1545 Intravenous vs Subcutaneous Infliximab for Inflammatory Bowel Disease: A Systematic Review and Meta-Analysis

Introduction: Infliximab, a tumor necrosis factor-alpha (TNF-α) inhibitor, is pivotal in managing inflammatory bowel disease (IBD), including Crohn’s disease (CD) and ulcerative colitis (UC). While the intravenous (IV) formulation has been standard, a subcutaneous (SC) form was recently approved, potentially offering greater convenience and healthcare efficiency. This meta-analysis compares the efficacy and safety of IV vs SC infliximab in IBD. Methods: A systematic search of PubMed and Scopus (through March 2025) identified randomized trials, cohorts, and observational studies involving adults with UC, CD, or IBD. Meta-analysis was conducted using R software (version 4.1.2). Relative risk (RR) and weighted mean difference (WMD) with 95% confidence intervals (CI) were used to assess dichotomous and continuous outcomes. Forest and funnel plots were generated. Heterogeneity was assessed using I² statistics. Risk of bias was evaluated with the Cochrane ROB 2 tool. Results: Seventeen studies (n = 2,885) met inclusion criteria. Pooled analysis showed significantly higher remission rates with IV infliximab (RR = 0.90; 95% CI: 0.83–0.97; I² = 68%; P < 0.01). Subgroup analysis by disease type (UC, CD, or IBD) revealed no significant effect modification (P = 0.48). Stratification by follow-up period showed a statistically significant difference favoring IV at 6 months. Injection-site reactions occurred in 24% of SC users (95% CI: 15%–34%), while infusion reactions occurred in 46% of IV users (95% CI: 36%–57%; I² = 0). Serious adverse events were reported in 23% of SC recipients (95% CI: 0%–48%), but inconsistent safety reporting limited comparisons. These findings contrast with a prior meta-analysis (Chetwood et al., J Crohn’s Colitis, 2024), which found no loss of remission after switching stable patients from IV to SC. Our broader analysis suggests IV may be more effective in achieving or maintaining remission. Conclusion: This meta-analysis indicates that IV infliximab is associated with significant improvement in remission rates compared to the SC form in IBD patients. Safety profiles differ, but inconsistent adverse event reporting limits definitive conclusions. Standardized efficacy and safety endpoints are essential in future comparative trials to guide optimal route selection.

Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001133640.46024.76
Primary Topic
Inflammatory Bowel Disease
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

S1545 Intravenous vs Subcutaneous Infliximab for Inflammatory Bowel Disease: A Systematic Review and Meta-Analysis

The American Journal of Gastroenterology
Inflammatory Bowel Disease
article

S1545 Intravenous vs Subcutaneous Infliximab for Inflammatory Bowel Disease: A Systematic Review and Meta-Analysis

article en

Abstract

Introduction: Infliximab, a tumor necrosis factor-alpha (TNF-α) inhibitor, is pivotal in managing inflammatory bowel disease (IBD), including Crohn’s disease (CD) and ulcerative colitis (UC). While the intravenous (IV) formulation has been standard, a subcutaneous (SC) form was recently approved, potentially offering greater convenience and healthcare efficiency. This meta-analysis compares the efficacy and safety of IV vs SC infliximab in IBD. Methods: A systematic search of PubMed and Scopus (through March 2025) identified randomized trials, cohorts, and observational studies involving adults with UC, CD, or IBD. Meta-analysis was conducted using R software (version 4.1.2). Relative risk (RR) and weighted mean difference (WMD) with 95% confidence intervals (CI) were used to assess dichotomous and continuous outcomes. Forest and funnel plots were generated. Heterogeneity was assessed using I² statistics. Risk of bias was evaluated with the Cochrane ROB 2 tool. Results: Seventeen studies (n = 2,885) met inclusion criteria. Pooled analysis showed significantly higher remission rates with IV infliximab (RR = 0.90; 95% CI: 0.83–0.97; I² = 68%; P < 0.01). Subgroup analysis by disease type (UC, CD, or IBD) revealed no significant effect modification (P = 0.48). Stratification by follow-up period showed a statistically significant difference favoring IV at 6 months. Injection-site reactions occurred in 24% of SC users (95% CI: 15%–34%), while infusion reactions occurred in 46% of IV users (95% CI: 36%–57%; I² = 0). Serious adverse events were reported in 23% of SC recipients (95% CI: 0%–48%), but inconsistent safety reporting limited comparisons. These findings contrast with a prior meta-analysis (Chetwood et al., J Crohn’s Colitis, 2024), which found no loss of remission after switching stable patients from IV to SC. Our broader analysis suggests IV may be more effective in achieving or maintaining remission. Conclusion: This meta-analysis indicates that IV infliximab is associated with significant improvement in remission rates compared to the SC form in IBD patients. Safety profiles differ, but inconsistent adverse event reporting limits definitive conclusions. Standardized efficacy and safety endpoints are essential in future comparative trials to guide optimal route selection.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 29%
Inflammatory Bowel Disease
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

S1545 Intravenous vs Subcutaneous Infliximab for Inflammatory Bowel Disease: A Systematic Review and Meta-Analysis · The American Journal of Gastroenterology (2025) | TGRS Research Map | TGRS