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Rituximab versus Azathioprine for Maintenance in ANCA-Associated Vasculitis

Open access
Guillevin, Loïc, Pagnoux, Christian, Karras, Alexandre, Khouatra, Chahera, Aumaître, Olivier, Cohen, Pascal, Maurier, François, Decaux, Olivier, Ninet, Jacques, Gobert, Pierre, Quémeneur, Thomas, Blanchard-Delaunay, Claire, Godmer, Pascal, Puéchal, Xavier, Carron, Pierre-Louis, Hatron, Pierre-Yves, Limal, Nicolas, Hamidou, Mohamed, Ducret, Maize, Daugas, Eric, Papo, Thomas, Bonnotte, Bernard, Mahr, Alfred, Ravaud, Philippe, Mouthon, Luc·2014·New England Journal of Medicine

Abstract

BACKGROUND: The combination of cyclophosphamide and glucocorticoids leads to remission in most patients with antineutrophil cytoplasm antibody (ANCA)-associated vasculitides. However, even when patients receive maintenance treatment with azathioprine or methotrexate, the relapse rate remains high. Rituximab may help to maintain remission. METHODS: Patients with newly diagnosed or relapsing granulomatosis with polyangiitis, microscopic polyangiitis, or renal-limited ANCA-associated vasculitis in complete remission after a cyclophosphamide-glucocorticoid regimen were randomly assigned to receive either 500 mg of rituximab on days 0 and 14 and at months 6, 12, and 18 after study entry or daily azathioprine until month 22. The primary end point at month 28 was the rate of major relapse (the reappearance of disease activity or worsening, with a Birmingham Vasculitis Activity Score >0, and involvement of one or more major organs, disease-related life-threatening events, or both). RESULTS: The 115 enrolled patients (87 with granulomatosis with polyangiitis, 23 with microscopic polyangiitis, and 5 with renal-limited ANCA-associated vasculitis) received azathioprine (58 patients) or rituximab (57 patients). At month 28, major relapse had occurred in 17 patients in the azathioprine group (29%) and in 3 patients in the rituximab group (5%) (hazard ratio for relapse, 6.61; 95% confidence interval, 1.56 to 27.96; P=0.002). The frequencies of severe adverse events were similar in the two groups. Twenty-five patients in each group (P=0.92) had severe adverse events; there were 44 events in the azathioprine group and 45 in the rituximab group. Eight patients in the azathioprine group and 11 in the rituximab group had severe infections, and cancer developed in 2 patients in the azathioprine group and 1 in the rituximab group. Two patients in the azathioprine group died (1 from sepsis and 1 from pancreatic cancer). CONCLUSIONS: More patients with ANCA-associated vasculitides had sustained remission at month 28 with rituximab than with azathioprine. (Funded by the French Ministry of Health; MAINRITSAN ClinicalTrials.gov number, NCT00748644; EudraCT number, 2008-002846-51.).

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Metadata

Authors
Guillevin, L., Pagnoux, C., Karras, A., Khouatra, C., Aumaître, O., Cohen, P., Maurier, F., Decaux, O., Ninet, J., Gobert, P., Quémeneur, T., Blanchard-Delaunay, C., Godmer, P., Puéchal, X., Carron, P.-L., Hatron, P.-Y., Limal, N., Hamidou, M., Ducret, M., Daugas, E., Papo, T., Bonnotte, B., Mahr, A., Ravaud, P., & Mouthon, L.
Venue
New England Journal of Medicine
Published
2014-11-06
Volume
371
Issue
19
Pages
1771-1780
ISSN
  • 0028-4793 (ISSN-L)
  • 1533-4406
OpenAlex
W2132820210
Cited by
1,090
References
1
FWCI
64.21
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Rituximab versus Azathioprine for Maintenance in ANCA-Associated Vasculitis. https://app.cochat.ai/papers/10.1056/nejmoa1404231
The paper
Guillevin, L., Pagnoux, C., Karras, A., Khouatra, C., Aumaître, O., Cohen, P., Maurier, F., Decaux, O., Ninet, J., Gobert, P., Quémeneur, T., Blanchard-Delaunay, C., Godmer, P., Puéchal, X., Carron, P.-L., Hatron, P.-Y., Limal, N., Hamidou, M., Ducret, M., . . . Mouthon, L. (2014). Rituximab versus Azathioprine for Maintenance in ANCA-Associated Vasculitis. New England Journal of Medicine. https://doi.org/10.1056/nejmoa1404231

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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