# Five-Year Persistence of Vedolizumab in Crohn’s Disease: Results from a Real-World Cohort

**Authors:** Marc Harb, Vinciane Muls, Alice Hoyois, Jennifer Aoun

PMC · DOI: 10.3390/jcm15041387 · Journal of Clinical Medicine · 2026-02-10

## TL;DR

This study shows that about 56% of Crohn’s disease patients stay on vedolizumab for 5 years, with early treatment response predicting long-term success.

## Contribution

The study provides real-world 5-year persistence data for vedolizumab in Crohn’s disease, identifying early response as a key predictor of long-term treatment success.

## Key findings

- 56.1% of patients remained on vedolizumab at 5 years.
- Early clinical and biological response at 12 and 24 months predicted long-term persistence.
- Male sex, longer disease duration, and absence of colonic disease were associated with better persistence.

## Abstract

Background: Vedolizumab (VDZ) is an α4β7 anti-integrin monoclonal antibody effective in Crohn’s disease (CD). While its short- and mid-term efficacy is well established, real-world data on long-term outcomes beyond 3 years are scarce. Recent studies suggest a progressive decline in persistence rates after 2 to 3 years, with very limited data beyond this period. The primary objective of this study was to evaluate the 5-year persistence of VDZ. Secondary objectives were to describe clinical, biological, and endoscopic responses at 2 years among patients remaining on treatment, and to identify predictors of long-term persistence, including the baseline Clinical Decision Support Tool (CDST) score. Methods: We conducted a retrospective observational study which included 60 adult patients with CD treated with VDZ before April 2025. Collected baseline variables included age, sex, BMI, smoking status, disease duration and location, prior biologic exposure, and CDST score. Treatment persistence was evaluated at 5 years. Clinical, biological, and endoscopic responses were assessed at 2 years. A global response was then defined as the achievement of a clinically significant improvement, normalization or marked reduction in inflammatory biomarkers, and endoscopic improvement. Predictors of persistence were also analyzed. Results: The mean age of this cohort was 45.4 ± 15.2 years, mean disease duration was 12.7 ± 10.1 years, and mean CDST score was calculated at 20.6 ± 2.7. At 5 years, 23/41 patients (56.1%) remained on VDZ therapy. Persistence was significantly associated with male sex (65.2% vs. 27.8%), longer disease duration (215 vs. 106 months), absence of rheumatologic manifestations (13.0% vs. 44.4%), and clinico-biological response at 12 months (65.2% vs. 30.8%). At 24 months, a global response was observed in all patients persisting at 5 years compared to 22.2% of those who discontinued (p < 0.001). At 2 years, 39/51 patients (76.5%) remained on VDZ. Persistence was associated with longer disease duration (189 vs. 75 months), male sex (61.5% vs. 25.0%), and absence of isolated colonic disease (0% vs. 16.7%). A global response at 2 years was achieved by 89.7% of persistent patients compared with none of the non-persistent group (p < 0.001). The CDST, uniformly elevated in this cohort, did not discriminate between persistent and non-persistent patients, but reflected appropriate initial patient selection. Conclusions: This real-world study documents 5-year outcome data on VDZ persistence in Crohn’s disease, a duration infrequently studied, with 56% of patients maintaining treatment. Early response at 12 and 24 months emerged as a key determinant of long-term persistence, highlighting the value of assessing 2-year outcomes to identify durable responders. Although not discriminatory in this homogeneous cohort, the CDST score emphasizes the potential role of predictive tools in guiding personalized therapeutic strategies. These results contribute to defining the long-term role of VDZ in the management of CD.

## Linked entities

- **Diseases:** Crohn’s disease (MONDO:0005011)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** IBD (MESH:D015212), spondyloarthritis (MESH:D013167), colonic disease (MESH:D003108), ileal disease (MESH:D007077), arthritis (MESH:D001168), inflammatory (MESH:D007249), injury to (MESH:D014947), CD (MESH:D003424), dermatologic (MESH:D000168), sacroiliitis (MESH:D058566), Rheumatologic (MESH:D012216)
- **Chemicals:** steroid (MESH:D013256), anti- (-), ustekinumab (MESH:D000069549), VDZ (MESH:C543529)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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## References

15 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942450/full.md

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Source: https://tomesphere.com/paper/PMC12942450