4.5 Article

Outcome After Discontinuation of TNFα-blocking Therapy in Patients with Inflammatory Bowel Disease in Deep Remission

Journal

INFLAMMATORY BOWEL DISEASES
Volume 20, Issue 6, Pages 1021-1028

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1097/MIB.0000000000000052

Keywords

Crohn's disease; ulcerative colitis; relapse; remission; TNF alpha-blocking therapy

Funding

  1. Abbvie
  2. MSD
  3. Tillotts Pharma
  4. Janssen
  5. Orion Pharma
  6. Medivir
  7. Roche
  8. Bayer
  9. Tillots Pharma
  10. GSK
  11. Almirall
  12. Shire
  13. Helsinki University Central Hospital Research Fund (EVO grant)
  14. Finnish Cultural Foundation
  15. Mary and George C. Ehrnrooth Foundation
  16. Finnish Foundation for Gastroenterological Research

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Background: Few data are available on the disease course in patients with inflammatory bowel disease (IBD) in deep remission after discontinuing tumor necrosis factor alpha (TNF alpha)-blocking therapy. In this prospective multicenter study, we evaluated the relapse rate, predictive factors, and the response to retreatment after discontinuation of TNF alpha-blocking therapy in patients with IBD in deep remission. Methods: We recruited 52 patients (17 Crohn's disease, 30 ulcerative colitis, and 5 IBD unclassified) in clinical, endoscopic, and fecal calprotectin-based (<100 mu g/g) remission after at least 1 year of TNF alpha-blocking therapy. Clinical and endoscopic remission and relapse were defined according to validated indices. After discontinuation of therapy, the patients were followed up with endoscopic assessment at 4 and 12 months. In the event of a clinical relapse with endoscopically active disease or minor clinical symptoms but severe endoscopic relapse, TNF alpha-blocking therapy was restarted. Results: After a median follow-up time of 13 (range, 12-15) months, 17/51 (33%) patients relapsed (5/17 Crohn's disease, 12/34 ulcerative colitis/IBD unclassified, 1 patient lost to follow-up at 6 mo). Ten experienced clinical and endoscopic relapse, 5 clinical relapse with mild endoscopic activity, and 2 severe endoscopic relapse. No specific predictive factors were associated with the relapse. Retreatment was effective in 94% of patients. Conclusions: After cessation of TNF alpha-blocking therapy in patients with IBD in deep remission, up to 67% remained in clinical remission during the 12-month follow-up. Importantly, 85% of these patients sustained endoscopic remission. The response to restart of TNF alpha antagonists was effective and well tolerated.

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