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Rituximab versus Cyclophosphamide for ANCA-Associated Vasculitis
- Source :
- New England Journal of Medicine, 363(3), 221-232. MASSACHUSETTS MEDICAL SOC
- Publication Year :
- 2010
-
Abstract
- Background Cyclophosphamide and glucocorticoids have been the cornerstone of remissioninduction therapy for severe antineutrophil cytoplasmic antibody (ANCA)−associated vasculitis for 40 years. Uncontrolled studies suggest that rituximab is effective and may be safer than a cyclophosphamide-based regimen. Methods We conducted a multicenter, randomized, double-blind, double-dummy, noninferiority trial of rituximab (375 mg per square meter of body-surface area per week for 4 weeks) as compared with cyclophosphamide (2 mg per kilogram of body weight per day) for remission induction. Glucocorticoids were tapered off; the primary end point was remission of disease without the use of prednisone at 6 months. Results Nine centers enrolled 197 ANCA-positive patients with either Wegener’s granulomatosis or microscopic polyangiitis. Baseline disease activity, organ involvement, and the proportion of patients with relapsing disease were similar in the two treatment groups. Sixty-three patients in the rituximab group (64%) reached the primary end point, as compared with 52 patients in the control group (53%), a result that met the criterion for noninferiority (P
- Subjects :
- medicine.medical_specialty
Cyclophosphamide
Gastroenterology
THERAPY
GRANULOMATOSIS ETANERCEPT TRIAL
WEGENERS-GRANULOMATOSIS
Prednisone
Internal medicine
medicine
Anti-neutrophil cytoplasmic antibody
business.industry
INDUCTION
General Medicine
REMISSION
medicine.disease
RANDOMIZED-TRIAL
Surgery
Regimen
B-CELLS
CELL-ACTIVATION
SYSTEMIC VASCULITIDES
Rituximab
business
Microscopic polyangiitis
Granulomatosis with polyangiitis
Vasculitis
ANTIBODY-ASSOCIATED VASCULITIS
medicine.drug
Subjects
Details
- Language :
- English
- ISSN :
- 00104299 and 00284793
- Database :
- OpenAIRE
- Journal :
- New England Journal of Medicine, 363(3), 221-232. MASSACHUSETTS MEDICAL SOC
- Accession number :
- edsair.doi.dedup.....2b62c3557c1b0b5c4c0a8c06967a5586