Brian G. Feagan, M.D., James Rochon, Ph.D., Richard N. Fedorak, M.D., E. Jan Irvine, M.D., Gary Wild, M.D., Lloyd Sutherland, M.D., A. Hillary Steinhart, M.D., Gordon R. Greenberg, M.D., Richard Gillies, M.D., Marybeth Hopkins, R.N., Stephen B. Hanauer, M.D., John W.D. McDonald, M.D., for The North American Crohn's Study Group Investigators
Background Although corticosteroids are highly effective inimproving symptoms of Crohn's disease, they may have substantialtoxicity. In some patients, attempts to discontinue corticosteroidsare unsuccessful.
Methods We conducted a double-blind, placebo-controlled multicenterstudy of weekly injections of methotrexate in patients who hadchronically active Crohn's disease despite a minimum of threemonths of prednisone therapy. Patients were randomly assignedto treatment with intramuscular methotrexate (25 mg once weekly)or placebo for 16 weeks. The patients also received prednisone(20 mg once a day), which was tapered over a period of 10 weeksunless their condition worsened. The primary outcome measurewas clinical remission at the end of the 16-week trial. Remissionwas defined by the discontinuation of prednisone and a scoreof <150 points on the Crohn's Disease Activity Index.
Results A total of 141 patients were randomly assigned in a2:1 ratio to methotrexate (94 patients) or placebo (47 patients).After 16 weeks, 37 patients (39.4 percent) were in clinicalremission in the methotrexate group, as compared with 9 patients(19.1 percent) in the placebo group (P = 0.025; relative risk,1.95; 95 percent confidence interval, 1.09 to 3.48). The patientsin the methotrexate group received less prednisone overall thanthose in the placebo group (P = 0.026). The mean (±SE)score on the Crohn's Disease Activity Index after 16 weeks oftreatment was significantly lower in the methotrexate group(162±12) than in the placebo group (204±17, P= 0.002). The changes in quality-of-life scores and serum orosomucoidconcentrations were similar. In the methotrexate group, 16 patients(17 percent) withdrew from treatment because of adverse events(including asymptomatic elevation of serum aminotransferasein 7 and nausea in 6), as compared with 1 patient (2 percent)in the placebo group.
Conclusions In a group of patients with chronically active Crohn'sdisease, methotrexate was more effective than placebo in improvingsymptoms and reducing requirements for prednisone.
Source Information
From the Department of Medicine, Division of Gastroenterology, University of Calgary, Calgary, Alta. (L.S.); the Department of Medicine, Section of Gastroenterology, University of Chicago, Chicago (S.B.H.); the Department of Medicine, Division of Gastroenterology, University of Alberta, Edmonton (R.N.F.); the Department of Medicine, Division of Gastroenterology, McMaster University, Hamilton, Ont. (E.J.I.); the Departments of Medicine (B.G.F., J.W.D.M., M.H.) and Epidemiology and Biostatistics (B.G.F., J.R.), University of Western Ontario, London, Ont.; the Department of Medicine, Division of Gastroenterology, McGill University, Montreal (G.W.); the Department of Medicine, Division of Gastroenterology, University of Toronto, Toronto (A.H.S., G.R.G.); and the Department of Medicine, University of Ottawa, Ottawa, Ont. (R.G.).
Address reprint requests to Dr. Feagan at 6 OF 12 University Hospital, 339 Windemere Rd., London, ON N6A 5A5, Canada.
Methotrexate for Crohn's Disease
Korelitz B. I., Present D. H., Feagan B. G., McDonald J. W.D., The North American Crohn's Study Group investigators
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