« Previous
Next »
Gastroenterology
Volume 142, Issue 1
, Pages 63-70.e5
, January 2012
Maintenance of Remission Among Patients With Crohn's Disease on Antimetabolite Therapy After Infliximab Therapy Is Stopped
References
- Maintenance infliximab for Crohn's disease: the ACCENT I randomised trial . Lancet . 2002;359:1541–1549
- Adalimumab for maintenance of clinical response and remission in patients with Crohn's disease: the CHARM trial . Gastroenterology . 2007;132:52–65
- Maintenance therapy with certolizumab pegol for Crohn's disease . N Engl J Med . 2007;357:239–250
- . Economic implications of biological therapies for Crohn's disease: review of infliximab . Pharmacoeconomics . 2005;23:875–888
- . Cost-effectiveness of biological therapy for Crohn's disease (Markov cohort analyses incorporating United Kingdom patient-level cost data) . Aliment Pharmacol Ther . 2009;30:265–274
- Risk of lymphoma associated with combination anti-tumor necrosis factor and immunomodulator therapy for the treatment of Crohn's disease: a meta-analysis . Clin Gastroenterol Hepatol . 2009;7:874–881
- Risk factors for opportunistic infections in patients with inflammatory bowel disease . Gastroenterology . 2008;134:929–936
- . Placental transport of immunoglobulins: a clinical review for gastroenterologists who prescribe therapeutic monoclonal antibodies to women during conception and pregnancy . Am J Gastroenterol . 2009;104:228–233
- Development of a Crohn's disease activity index . Gastroenterology . 1976;70:439–444
- . Development and validation of a Crohn's disease endoscopic index: a prospective multicentric study . Gut . 1989;30:983–989
- An enzyme-linked immunosorbent assay for therapeutic drug monitoring of infliximab . Ther Drug Monit . 2006;28:169–174
- Withdrawal of immunosuppression in Crohn's disease treated with scheduled infliximab maintenance: a randomized trial . Gastroenterology . 2008;134:1861–1868
- . Sample-size formulation for the proportional-hazards regression model . Biometrics . 1983;39:499–503
-
.
Nonparametric estimation for incomplete observations
.
J Am Stat Assoc
. 1958;53:457–481
-
.
Regression models and life-tables (with discussions), series B
.
J R Stat Soc
. 1972;34:184–192
- . Imputing missing covariate values for the Cox model . Stat Med . 2009;28:1982–1998
- . Proportional hazards tests and diagnostics based on weighted residuals . Biometrika . 1994;81:515–526
- . Concordance probability and discriminatory power in proportional hazards regression . Biometrika . 2005;92:965–970
-
.
An introduction to the bootstrap
.
In: New York, NY: Chapman & Hall; 1990;p. 17
-
.
Nonparametric statistics for the behavioral sciences
.
In: New York, NY: McGraw-Hill; 1956;p. 75–83
- . Loss of response and requirement of infliximab dose intensification in Crohn's disease: a review . Am J Gastroenterol . 2009;104:760–767
- Association of trough serum infliximab to clinical outcome after scheduled maintenance treatment for Crohn's disease . Clin Gastroenterol Hepatol . 2006;4:1248–1254
- Hydrocortisone intravenous premedication reduces antibodies to infliximab in Crohn's disease: a randomized controlled trial . Gastroenterology . 2003;124:917–924
- Effect of discontinuing TNFalpha antagonist therapy in patients with remission of rheumatoid arthritis . Joint Bone Spine . 2009;76:350–355
-
Safety and efficacy of readministration of infliximab after longterm continuous therapy and withdrawal in patients with ankylosing spondylitis
.
J Rheumatol
. 2007;34:510–515
- The tolerance and efficacy of a postponed retreatment with infliximab in Crohn's disease primary responders . Aliment Pharmacol Ther . 2009;29:1240–1248
- Infliximab reintroduction is not associated to a higher rate of immune-related adverse effects in patients with inflammatory bowel disease initially treated with a three-infusion induction regimen . J Clin Gastroenterol . 2010;44:34–37
- Discontinuation of infliximab after attaining low disease activity in patients with rheumatoid arthritis: RRR (remission induction by Remicade in RA) study . Ann Rheum Dis . 2010;69:1286–1291
This article has an accompanying continuing medical education activity on page e31. Learning Objective: Upon completion of this exercise, successful learners will be able to assess the risk of relapse and the response to potential re-treatment in Crohn's disease patients in whom infliximab treatment would be stopped after prolonged stable remission under combined therapy with antimetabolite and infliximab.
Conflicts of interest The authors disclose the following: E.L. has received consultancy fees from Schering-Plough, Abbott Laboratories, MSD, Ferring Pharmaceuticals, Shire, Millennium Pharmaceuticals, and UCB; research or educational grants from MSD, Schering-Plough, AstraZeneca, and Abbott Laboratories; and lecture fees from Abbott Laboratories, AstraZeneca, Ferring Pharmaceuticals, MSD, Schering-Plough, Falk, Menarini, Chiesi, and Nycomed. Y.B. has received consultancy fees and lecture fees from Norgine, Abbott Laboratories, Schering-Plough, and Ferring Pharmaceuticals. D.L. has received consultancy fees from Norgine and Ferring Pharmaceuticals and has received lecture fees from Norgine, Ferring Pharmaceuticals, Abbott Laboratories, and Schering-Plough. G.S. has received lecture fees from Abbott Laboratories and Schering-Plough. M.D. has received an educational grant from Schering-Plough. G.P. has received consultancy fees from Roche and LFB and has received lecture fees from Janssen-Cilag. J.-F.C. has received consulting fees from Abbott Laboratories, ActogeniX, Albireo Pharma, Amgen, AstraZeneca, Bayer AG, Biogen Idec, Boehringer Ingelheim GmbH, Bristol-Myers Squibb, Cellerix, Centocor, ChemoCentryx, Cosmo Technologies, Danone Research, Elan Pharmaceuticals, Genentech, Giuliani SpA, Given Imaging, GlaxoSmithKline, Hutchison MediPharma, Merck Sharp & Dohme Corp, Millennium Pharmaceuticals (now Takeda), Neovacs, Ocera Therapeutics, Pfizer, Shire Pharmaceuticals, Prometheus Laboratories, Sanofi-Aventis, Schering-Plough, Synta Pharmaceuticals Corp, Teva, Therakos, UCB Pharma, and Wyeth; has served on advisory committees for Abbott Laboratories, Centocor, Danone Research, Elan Pharmaceuticals, Merck Sharp & Dohme, Millennium Pharmaceuticals (now Takeda), Schering-Plough, and UCB Pharma; has received speaking fees from Abbott Laboratories, Centocor, Elan Pharmaceuticals, Given Imaging, Merck Sharp & Dohme Corp, Otsuka America Pharmaceutical, Schering-Plough, Shire Pharmaceuticals, Tillotts Pharma, and UCB Pharma; and has received grant support from Abbott Laboratories, AstraZeneca, Ferring Pharmaceuticals, Merck Sharp & Dohme Corp, Schering-Plough, and UCB Pharma. The remaining authors disclose no conflicts.
Funding The GETAID received unrestricted study grants from the Association François Aupetit and the Société Nationale Française de Gastroentérologie.
PII: S0016-5085(11)01293-5
doi: 10.1053/j.gastro.2011.09.034
© 2012 AGA Institute. Published by Elsevier Inc. All rights reserved.
« Previous
Next »
Gastroenterology
Volume 142, Issue 1
, Pages 63-70.e5
, January 2012

