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Journal of the Canadian Association of Gastroenterology logoLink to Journal of the Canadian Association of Gastroenterology
. 2026 Feb 13;9(Suppl 1):gwaf042.276. doi: 10.1093/jcag/gwaf042.276

Poster Session II - A276 COMPARISON OF PATIENT RESPONSE TO FIRST VERSUS SECOND-LINE INFLIXIMAB IN MODERATE-TO-SEVERE ULCERATIVE COLITIS: A RETROSPECTIVE STUDY

C Galts 1, S Anvari 2, M Haq 3, K Grossman 4, D Borovsky 5, A Wen 6, E Wong 7, H R Tran 8, A Albassam 9, S Halder 10, J Marshall 11, N Narula 12
PMCID: PMC12901628

Abstract

Background

Infliximab has remained a cornerstone in the management of moderate and/or severe ulcerative colitis (UC), however its outcomes after other advanced therapy failure has not been evaluated comprehensively

Aims

This study evaluates infliximab’s second-line effectiveness, identifies predictors of response, and compares outcomes to its first-line use.

Methods

A retrospective cohort study of adults with moderate or severe UC and treated with infliximab was identified at a tertiary care center between 2016-2024. Those patients were then categorized by line of therapy. Multivariable logistic regression was used to assess predictors of one-year clinical remission

Results

Among the 225 patients who met the study criteria, 143 (63.6%) received infliximab as first-line and 82 (36.4%) as second-line or subsequent therapy (Table 1). Clinical response at one year was significantly lower in second-line users (odds ratio 0.53, 95%CI 0.28–0.99, p = 0.049), and remained significantly lower after adjustment for biosimilar and concurrent steroid use. Other outcomes including one-year clinical remission, endoscopic improvement or remission were not significant (OR 0.69 (95% CI 0.44-1.08), p = 0.102; OR 0.84 (95% CI 0.50-1.43), p = 0.522; OR 0.79 (95% CI 0.46-1.34), p = 0.378; respectively). There was significantly more dose escalation of infliximab within one year (p = 0.049) among patients who had prior advanced therapy, as well as more discontinuation of infliximab within one year (p = 0.045), compared with first-line infliximab treated patients (Figure 1).

Conclusions

Infliximab continues to demonstrate high rate of clinical and endoscopic response, however its clinical response is significantly lower than in patients who received infliximab first-line. These findings support its continued use while highlighting the need for optimized patient selection and treatment strategies in therapy-exposed populations.

A276 Table 1: Baseline characteristics

Variable Overall (n = 225) First-line infliximab (n = 143) Second-line infliximab + (n = 82) p-value
Age at diagnosis, mean (SD) 31.3 (14.4) 32.0 (14.4) 30.1 (14.5) 0.345
Female, n (%) 103 (45.8) 65 (45.5) 38 (46.3) 0.898
Disease extent, n (%) 0.704
Proctitis 24 (10.8) 17/142 (12.0) 7/81 (8.6)
Left-sided 72 (32.3) 47/142 (33.1) 25/81 (30.8)
Pancolitis 127 (57.0) 78/142 (54.9) 49/81 (60.5)
Smoker, n (%) 22 (10.0) 10/140 (7.1) 12/80(15.0) 0.086
Infliximab started as in-patient, n (%) 64 (28.4) 51 (35.7) 13 (15.9) 0.002
Concurrent azathioprine, 6-MP or methotrexate while on infliximab, n (%) 78 (34.7) 53 (37.1) 25 (30.5) 0.315
Concurrent steroid use > 10mg/d at induction, n (%) 57 (25.3) 33 (23.1) 24 (29.3) 0.308

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Funding Agencies

None


Articles from Journal of the Canadian Association of Gastroenterology are provided here courtesy of Oxford University Press

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