Infliximab as Rescue Therapy in Severe to Moderately Severe Ulcerative Colitis: A Randomized, Placebo-Controlled Study
Received 9 November 2004; accepted 23 February 2005.
Refers to article:
Infliximab for Ulcerative Colitis: Finally Some Answers
Geert D’haens
Gastroenterology
June 2005 (Vol. 128, Issue 7, Pages 2161-2164) Full Text |
Full-Text PDF (81 KB)
Background & Aims: Despite treatment with corticosteroids, severe to moderately severe attacks of ulcerative colitis have a high colectomy rate. We intended to find a rescue therapy other than cyclosporin A, which imposes a high risk of side effects and cyclosporine-related mortality. Methods: This was a randomized double-blind trial of infliximab or placebo in severe to moderately severe ulcerative colitis not responding to conventional treatment. Patients were randomized to infliximab/placebo either on day 4 after the initiation of corticosteroid treatment if they fulfilled the index criteria for fulminant ulcerative colitis on day 3 or on day 6–8 if they fulfilled index criteria on day 5–7 for a severe or moderately severe acute attack of ulcerative colitis. Results were analyzed according to the intention-to-treat principle. The primary end point was colectomy or death 3 months after randomization. Secondary end points were clinical and endoscopic remission at that time in patients who did not undergo operation. Results: Forty-five patients were included (24 infliximab and 21 placebo). No patient died. Seven patients in the infliximab group and 14 in the placebo group had a colectomy (P = .017; odds ratio, 4.9; 95% confidence interval, 1.4–17) within 3 months after randomization. No serious side effects occurred. Three patients in the placebo group required operation for septic complications. Conclusions: Infliximab 4–5 mg/kg is an effective and safe rescue therapy in patients experiencing an acute severe or moderately severe attack of ulcerative colitis not responding to conventional treatment.
⁎Department of Medicine, Division of Gastroenterology, Örebro University Hospital, Örebro, Sweden
‡Department of Medicine, Division of Gastroenterology, Lund University Hospital, Lund, Sweden
§Department of Medicine, Division of Gastroenterology, Sahlgrenska University Hospital, Gothenburg, Sweden
‖Department of Gastroenterology and Hepatology, Karolinska University Hospital, Stockholm, Sweden
¶Department of Medicine, Division of Gastroenterology, South Hospital, Stockholm, Sweden
#Department of Medicine, Division of Gastroenterology, Ryhov Hospital, Jönköping, Sweden
⁎⁎Department of Medicine, Division of Gastroenterology, West Zealand Hospital, Slagelse, Denmark
‡‡Department of Molecular and Clinical Medicine, Division of Gastroenterology and Hepatology, Faculty of Health Sciences, Linköping, Sweden
§§Department of Medicine, Division of Gastroenterology, Umeå University Hospital, Umeå, Sweden
‖‖Department of Medicine, Division of Gastroenterology, Malmö General University Hospital, Malmö, Sweden
¶¶Unit of Statistics and Epidemiology, Centre for Clinical Research, Örebro University Hospital, Örebro, Sweden
Address requests for reprints to: Gunnar Järnerot, MD, PhD, FRCP, Department of Medicine, Division of Gastroenterology, Örebro University Hospital, S-701 85 Örebro, Sweden.
Supported by the Swedish Federation of County Councils, Örebro County Research Foundation, Schering-Plough AB, Sweden, Clinical Research Centre, Örebro University Hospital, the Medical Research Council of Southeast Sweden, Foundation of Medical Science Region 3, Denmark (Grant 2-47-19-02), and participating hospitals (infliximab/placebo).