Discontinuation of Infliximab Therapy in Patients with Crohn’s Disease

  • Buhl Sine
  • , Steenholdt Casper
  • , Brynskov Jørn
  • , Christensen Katrine Risager
  • , Dorn-Rasmussen Maria
  • , Thomsen Ole Østergaard
  • , Bendtzen Klaus
  • , Klausen Tobias Wirenfeldt
  • , Dahlerup Jens Frederik
  • , Thorsgaard Niels
  • , Jahnsen Jørgen
  • , Molazahi Akbar
  • , Pedersen Natalia
  • , Kjeldsen Jens
  • , Almer Sven
  • , Dahl Eva Efsen
  • , Vind Ida
  • , Cannon Annett Gerhardt
  • , Marsal Jan
  • , Sipponen Taina
  • Agnholt Jørgen Steen, Kievit Hendrika Adriana Linda, Aure Synnøve Louise, Martinsen Lars, Meisner Svetlana, Hansen Jane Møller, Ainsworth Mark Andrew*, Stop Infliximab Treatment (STOP-IT) study group
*Kontaktforfatter

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

Abstract

BACKGROUND
Whether infliximab therapy can be successfully discontinued after patients with Crohn’s disease have attained sustained, clinical, biochemical, and endoscopic remission is unknown.

METHODS
We conducted a multicenter, randomized, double-blind, placebo-controlled withdrawal study of infliximab in patients with Crohn’s disease who were in clinical, biochemical, and endoscopic remission after standard infliximab maintenance therapy for at least 1 year. Patients were randomly assigned 1:1 to continue infliximab therapy or to receive matching placebo for 48 weeks. The primary end point was time to relapse.

RESULTS
This study randomly assigned 115 patients to either the infliximab-continuation group or to the infliximab-discontinuation group. No relapses were observed among the 59 patients continuing infliximab, whereas 23 of 56 patients discontinuing infliximab experienced relapse. Time to relapse was significantly shorter among patients who discontinued infliximab than among those who continued infliximab (hazard ratio, 0.080; 95% confidence interval [CI], 0.035 to 0.186; P<0.001). At the end of the trial at week 48, relapse-free survival was 100% in the infliximab-continuation group and 51% in the infliximab-discontinuation group. The key secondary end point, time to loss of remission, was significantly shorter among patients discontinuing infliximab therapy than those continuing infliximab (hazard ratio, 0.025; 95% CI, 0.003 to 0.187; P<0.001). No unexpected adverse events were reported.

CONCLUSIONS
Discontinuation of infliximab for patients with Crohn’s disease receiving long-term infliximab therapy and in clinical, biochemical, and endoscopic remission leads to a considerable risk of relapse.
OriginalsprogEngelsk
ArtikelnummerEVIDoa2200061
TidsskriftNEJM Evidence
Vol/bind1
Udgave nummer8
ISSN2766-5526
DOI
StatusUdgivet - aug. 2022

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