Biologic Therapy for Inflammatory Bowel Disease: Real-World Comparative Effectiveness and Impact of Drug Sequencing in 13 222 Patients within the UK IBD BioResource

Christina Kapizioni, Rofaida Desoki, Danielle Lam, Karthiha Balendran, Eman Al-Sulais, Sreedhar Subramanian, Joanna E Rimmer, Juan De La Revilla Negro, Holly Pavey, Laetitia Pele, Johanne Brooks, Gordon W Moran, Peter M Irving, Jimmy K Limdi, Christopher A Lamb, Miles Parkes, Tim Raine

Research output: Contribution to journalArticlepeer-review

60 Citations (Scopus)
3 Downloads (Pure)

Abstract

BACKGROUND AND AIMS: This study compares the effectiveness of different biologic therapies and sequences in patients with inflammatory bowel disease [IBD] using real-world data from a large cohort with long exposure.

METHODS: Demographic, disease, treatment, and outcome data were retrieved for patients in the UK IBD BioResource. Effectiveness of treatment was based on persistence free of discontinuation or failure, analysed by Kaplan-Meier survival analysis with inverse probability of treatment weighting to adjust for differences between groups.

RESULTS: In total, 13 222 evaluable patients received at least one biologic. In ulcerative colitis [UC] first-line vedolizumab [VDZ] demonstrated superior effectiveness over 5 years compared to anti-tumour necrosis factor [anti-TNF] agents [p = 0.006]. VDZ was superior to both infliximab [IFX] and adalimumab [ADA] after ADA and IFX failure respectively [p < 0.001 and p < 0.001]. Anti-TNF therapy showed similar effectiveness when used as first-line treatment, or after failure of VDZ. In Crohn's disease [CD] we found significant differences between first-line treatments over 10 years [p = 0.045], with superior effectiveness of IFX compared to ADA in perianal CD. Non-anti-TNF biologics were superior to a second anti-TNF after first-line anti-TNF failure in CD [p = 0.035]. Patients with UC or CD experiencing TNF failure due to delayed loss of response or intolerance had superior outcomes when switching to a non-anti-TNF biologic, rather than a second anti-TNF.

CONCLUSIONS: We provide real-world evidence to guide biologic selection and sequencing in a range of common scenarios. Our findings challenge current guidelines regarding drug selection after loss of response to first anti-TNF treatment.
Original languageEnglish
Pages (from-to)790-800
Number of pages11
JournalJournal of Crohn's & Colitis
Volume18
Issue number6
Early online date2 Dec 2023
DOIs
Publication statusPublished - 30 Jun 2024

Keywords

  • Humans
  • Male
  • Female
  • Adalimumab/therapeutic use
  • Antibodies, Monoclonal, Humanized/therapeutic use
  • Infliximab/therapeutic use
  • United Kingdom
  • Adult
  • Colitis, Ulcerative/drug therapy
  • Middle Aged
  • Gastrointestinal Agents/therapeutic use
  • Crohn Disease/drug therapy
  • Tumor Necrosis Factor-alpha/antagonists & inhibitors
  • Biological Products/therapeutic use
  • Treatment Outcome
  • Biological Therapy/methods
  • Inflammatory Bowel Diseases/drug therapy
  • Etanercept/therapeutic use
  • Tumor Necrosis Factor Inhibitors/therapeutic use

Fingerprint

Dive into the research topics of 'Biologic Therapy for Inflammatory Bowel Disease: Real-World Comparative Effectiveness and Impact of Drug Sequencing in 13 222 Patients within the UK IBD BioResource'. Together they form a unique fingerprint.

Cite this