Abstract Background Subcutaneous infliximab (SC-IFX) offers an alternative to intravenous therapy with potential advantages in treatment persistence, medication burden and patient adherence. This study evaluated 12-month treatment persistence along with clinical, biochemical, and endoscopic outcomes among patients with inflammatory bowel disease (IBD) established on SC-IFX monotherapy. Methods A retrospective observational cohort study was conducted at a tertiary centre. Baseline clinical (CDAI or partial Mayo score), biochemical (C-reactive protein, albumin, haemoglobin, faecal calprotectin, IFX trough levels) and endoscopic data were collected at index of SC-IFX commencement and at 12-months. Logistic regression analysis was used to identify predictors of treatment discontinuation. Results 101 adult patients were on SC-IFX monotherapy, 57 (56.4%) had Crohn’s Disease and 44 (43.6%) had Ulcerative Colitis. Treatment persistence at 12 months was 91.1% (92/101), with sustained or improved clinical (100/101, 99.0%), biochemical (CRP (87/101, 88.1%), albumin (97/101, 96.0%), haemoglobin (100/101, 99.0%), faecal calprotectin (87/95, 91.6%), infliximab trough levels (86/94, 91.5%) and endoscopic activity (90/93, 96.8%) outcomes at 12 months. Multivariate regression analysis only identified prior ileal resection as an independent predictor of treatment discontinuation at 12-months. Conclusion • Real-world study demonstrating high 12-month persistence of SC-IFX monotherapy with and maintenance of clinical, biochemical, and endoscopic outcomes at 12 months. • Stable pharmacokinetic profile (higher, more consistent trough levels) likely underpins durability and may reduce need for immunomodulators. • Clinical relevance: potential practical long-term maintenance option, avoids immunomodulator risks (infection, malignancy), improves convenience, reduces infusion burden. • Limitations: retrospective single-centre design, modest sample size. • Future directions: longer-term outcomes, larger multicentre studies, exploration of predictors of treatment discontinuation and pharmacogenomics. Conflict of interest: Dr. Mansoor, Matthew: No conflict of interest Subhaharan, Deloshaan: No conflict of interest James, Rayshelle: No conflict of interest Kakkadasam Ramaswamy, Pradeep: No conflict of interest Mohsen, Waled: No conflict of interest
Mansoor et al. (Thu,) studied this question.