Journal Article10.1056/NEJMOA020286
A Randomized Trial of Maintenance Therapy for Vasculitis Associated with Antineutrophil Cytoplasmic Autoantibodies
David Jayne,Niels Rasmussen,Konrad Andrassy,Paul A. Bacon,Jan Willem Cohen Tervaert,J. Dadoniene,Agneta Ekstrand,Gill Gaskin,Gina Gregorini,Kirsten de Groot,Wolfgang L. Gross,E. Christiaan Hagen,Eduardo Mirapeix,Erna Pettersson,Carl Siegert,Alberto Sinico,Vladimir Tesar,Kerstin Westman,Charles D. Pusey +18 more
TL;DR: In patients with generalized vasculitis, the withdrawal of cyclophosphamide and the substitution of azathioprine after remission did not increase the rate of relapse, suggesting the duration of exposure to cycloph phosphamide may be safely reduced.
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Abstract: Background The primary systemic vasculitides usually associated with autoantibodies to neutrophil cytoplasmic antigens include Wegener's granulomatosis and microscopic polyangiitis. We investigated whether exposure to cyclophosphamide in patients with generalized vasculitis could be reduced by substitution of azathioprine at remission. Methods We studied patients with a new diagnosis of generalized vasculitis and a serum creatinine concentration of 5.7 mg per deciliter (500 μmol per liter) or less. All patients received at least three months of therapy with oral cyclophosphamide and prednisolone. After remission, patients were randomly assigned to continued cyclophosphamide therapy (1.5 mg per kilogram of body weight per day) or a substitute regimen of azathioprine (2 mg per kilogram per day). Both groups continued to receive prednisolone and were followed for 18 months from study entry. Relapse was the primary end point. Results Of 155 patients studied, 144 (93 percent) entered remission and were randoml...
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ANCA Glomerulonephritis and Vasculitis
TL;DR: There is clinical, in vitro, and animal model evidence that ANCAs cause disease by activating neutrophils to attack small vessels, and there have been major advances in optimizing treatment by minimizing toxic therapy and utilizing more targeted therapy.
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Churg-strauss syndrome with poor-prognosis factors : A prospective multicenter trial comparing glucocorticoids and six or twelve cyclophosphamide pulses in forty-eight patients
Pascal Cohen,Christian Pagnoux,Alfred Mahr,Jean-Pierre Arène,Luc Mouthon,Véronique Le Guern,M. André,M. Gayraud,David Jayne,Daniel Engelbert Blockmans,Jean-François Cordier,Loïc Guillevin +11 more
TL;DR: It was concluded that 12 cyclophosphamide pulses were better able to control severe CSS than a 6-pulse regimen, and the optimal duration of therapy remains to be determined.
310
Antineutrophil cytoplasm antibodies directed against myeloperoxidase augment leukocyte-microvascular interactions in vivo
Mark A. Little,C. Lucy Smyth,Rashmi Yadav,Lyn R. Ambrose,H. Terence Cook,Sussan Nourshargh,Charles D. Pusey +6 more
TL;DR: This study provides the first direct in vivo evidence for the ability of ANCAs to enhance leukocyte-endothelial interactions and cause microvascular hemorrhage, thereby providing a mechanism by which ANCAs could exert pathogenic effects in systemic vasculitis.
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Javier D. Finkielman,Peter A. Merkel,Darrell R. Schroeder,Gary S. Hoffman,Robert Spiera,E. William St. Clair,John C. Davis,W. Joseph McCune,Andrea Lears,Steven R. Ytterberg,Amber M. Hummel,Margaret A. Viss,Tobias Peikert,John H. Stone,Ulrich Specks +14 more
TL;DR: This prospective study sought to determine whether pro-PR3ANCA levels correlate more strongly with disease activity than do mature- PR3AnCA levels, whether a decrease in pro- or mature-PR2ANCA Levels during remission-induction therapy is associated with a shorter time to sustained remission, and whether an increase in pro/or mature-pr3AN CA levels is associatedWith relapse.
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Incidence and survival rates in Wegener's granulomatosis, microscopic polyangiitis, Churg–Strauss syndrome and polyarteritis nodosa
TL;DR: The incidence of WG and MPA was equal in the authors' district, but there was a difference in survival rates related to age and renal function, which was not significant in the multivariate analysis.
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