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Rheumatology Advance Access originally published online on May 22, 2007
Rheumatology 2007 46(7):1087-1091; doi:10.1093/rheumatology/kem029
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© The Author 2007. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Elevated relapse rate under oral methotrexate versus leflunomide for maintenance of remission in Wegener's granulomatosis

C. Metzler, N. Miehle1, K. Manger2, C. Iking-Konert3, K. de Groot4, B. Hellmich, W. L. Gross, E. Reinhold-Keller and for the German Network of Rheumatic Diseases

Department of Rheumatology, University Hospital of Schleswig-Holstein, Campus Luebeck and Rheumaklinik Bad Bramstedt, 1Department of Rheumatology and Clinical Immunology, University of Freiburg, 2Department of Rheumatology, University of Erlangen, 3Department of Endocrinology, Diabetes and Rheumatology, University of Düsseldorf, 4Department of Nephrology and Rheumatology, Hospital Offenbach.

Correspondence to: C. Metzler, MD, Department of Rheumatology, University Hospital of Schleswig-Holstein, Campus Luebeck, Ratzeburger Allee 160, D-23538 Luebeck, Germany. E-mail: cmetzler{at}foni.net


   Abstract

Objectives. Results from open-label trials suggest that methotrexate (MTX) and leflunomide (LEF) are effective for maintenance of remission in Wegener's granulomatosis (WG), but data from randomized controlled clinical trails are not yet available.

Methods. In this multicentre, prospective randomized controlled clinical trial, patients with generalized WG were treated either with oral LEF 30 mg/day or oral MTX (starting with 7.5 mg/week reaching 20 mg/week after 8 weeks) for 2 yrs following induction of remission with cyclophosphamide. The primary endpoint was the incidence of relapses. Secondary outcome parameters were DEI, BVAS, SF-36, cANCA-titre, ESR and CRP.

Results. Fifty-four patients were included in the study, 26 in the LEF-limb, 28 in the MTX-limb. In the LEF-group, six patients relapsed after a median time of 7 months, thereof one major relapse with a new pulmonary manifestation. In the MTX-group, 13 relapses occurred in 6 months, of which seven were major: rapidly progressive glomerulonephritis (n = 4), pulmonary haemorrhage (n = 2) and one cerebral granuloma. The significantly higher incidence of major relapses in the MTX-limb (P = 0.037) led to premature termination of the study. In the LEF-limb, four patients were withdrawn due to hypertension (n = 2), peripheral neuropathy (n = 1) and leucopenia (n = 1).

Conclusion. LEF at a dosage of 30 mg/day appears to be effective in the prevention of major relapses in WG, however, this is associated with an increased frequency of adverse events. Further studies testing other dosing regimens of lower doses of LEF are needed to confirm these promising results in larger patients cohorts.

KEY WORDS: Wegener's granulomatosis, Remission, Relapse, Methotrexate, Leflunomide

Submitted 17 May 2006; revised version accepted 16 January 2007.
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