4.7 Article

Impact of vedolizumab therapy on extra-intestinal manifestations in patients with inflammatory bowel disease: a multicentre cohort study nested in the OBSERV-IBD cohort

Journal

ALIMENTARY PHARMACOLOGY & THERAPEUTICS
Volume 47, Issue 4, Pages 485-493

Publisher

WILEY
DOI: 10.1111/apt.14419

Keywords

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Funding

  1. Abbvie
  2. Hospira
  3. Takeda
  4. Gilead
  5. Biocodex
  6. Janssen
  7. Ferring
  8. MSD
  9. Merck
  10. Genentech
  11. Norgine
  12. Tillots
  13. Vifor
  14. Shire
  15. Therakos
  16. Pharmacosmos
  17. Pilege
  18. BMS
  19. UCB-Pharma
  20. Celltrion
  21. Biogaran
  22. Boerhinger-Ingelheim
  23. Lilly
  24. Pfizer
  25. HAC-Pharma
  26. Janssen Cilag
  27. Mitsubishi
  28. Astellas Pharma
  29. Covidien
  30. Jansen Cilag
  31. Vifor Pharma
  32. Mayoly Spindler
  33. Novo Nordisk
  34. GSK
  35. UCB
  36. HAC Pharma
  37. Ferring France
  38. MSD France
  39. Sanofi
  40. Norgine Pharma
  41. Astra Zeneca
  42. Roche
  43. Takeda Millenium
  44. Falk
  45. Given Imaging

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Background: The effectiveness of vedolizumab as a treatment for extraintestinal manifestations (EIM) is questionable due to its gut-specificity. Aim: To assess effectiveness of vedolizumab for EIM in patients with inflammatory bowel disease (IBD) in a large real-life experience cohort. Methods: Between June and December 2014, 173 patients with Crohn's disease and 121 with ulcerative colitis were treated with vedolizumab. Patients were followed until week 54. EIM activity was assessed at weeks 0, 6, 14, 22, 30 and 54 by using a 3-step scale: complete remission, partial response and no response. Results: At baseline, 49 (16.7%) patients had EIMs of which 47 had inflammatory arthralgia/arthritis, four had cutaneous lesions and two had both rheumatologic and skin EIM. At week 54, 21 (44.7%) patients had complete remission for inflammatory arthralgia/arthritis and three (75%) for cutaneous EIM. In multivariate analysis, complete remission of inflammatory arthralgia/arthritis was associated with clinical remission of IBD (OR = 1.89, IC95% [1.05-3.41], P = .03) and recent onset of inflammatory arthralgia/arthritis (OR = 1.99, IC95% [1.12-3.52], P = .02). During the follow-up period, 34 (13.8%) patients without any EIM at baseline, developed incident cases of inflammatory arthralgia/arthritis consisting mostly of peripheral arthralgia without evidence of arthritis and 14 (4.8%) incident cases of paradoxical skin manifestation. Conclusion: Vedolizumab therapy is commonly associated with improvement in EIM. This was associated with quiescent IBD and recent EIM. However, paradoxical skin manifestation and inflammatory arthralgia/arthritis may occur upon vedolizumab therapy.

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