Rituximab versus Azathioprine for Maintenance in ANCA-Associated Vasculitis

被引:758
|
作者
Guillevin, L. [1 ]
Pagnoux, C. [1 ,23 ]
Karras, A. [2 ]
Khouatra, C. [6 ,24 ]
Aumaitre, O. [8 ]
Cohen, P. [1 ]
Maurier, F. [9 ]
Decaux, O. [10 ]
Ninet, J. [7 ]
Gobert, P. [11 ]
Quemeneur, T. [12 ,13 ]
Blanchard-Delaunay, C. [14 ]
Godmer, P. [15 ]
Puechal, X. [1 ]
Carron, P. -L. [16 ]
Hatron, P. -Y. [17 ]
Limal, N. [18 ]
Hamidou, M. [19 ]
Ducret, M. [20 ]
Daugas, E. [3 ]
Papo, T. [4 ]
Bonnotte, B. [21 ,22 ]
Mahr, A. [1 ]
Ravaud, P. [5 ]
Mouthon, L. [1 ]
机构
[1] Univ Paris 05, Hop Cochin, Sorbonne Paris Cite,Dept Med Interne, Ctr Reference Malad Autoimmunes Rares,INSERM,U101, Paris, France
[2] Univ Paris 05, Hop Europeen Georges Pompidou, Nephrol Unit, Paris, France
[3] Univ Paris 05, Hop Bichat, Serv Nephrol, Dept Hospitalo Univ FIRE,INSERM,U699, Paris, France
[4] Hop Cochin, Dept Med Interne, F-75674 Paris, France
[5] Univ Paris 05, Hop Hotel Dieu, Ctr Epidemiol Clin, INSERM,U738, Paris, France
[6] Hop Univ Louis Pradel, Ctr Reference Malad Pulm Rares, Serv Pneumol, Lyon, France
[7] Hop Edouard Herriot, Serv Med Interne, Lyon, France
[8] Hop Gabriel Montpied, Ctr Hosp Univ, Clermont Ferrand, France
[9] Hop Prives Metz, Serv Med Interne, Metz, France
[10] Univ Rennes 1, Hop Sud, Hop Univ Rennes, Dept Med Interne,IGDR UMR 6290, Rennes, France
[11] Hop Gen Henri Duffaut, Serv Med Interne & Nephrol, Avignon, France
[12] Ctr Hosp Valenciennes, Dept Nephrol, Valenciennes, France
[13] Ctr Hosp Valenciennes, Dept Med Interne, Valenciennes, France
[14] Ctr Hosp Gen Niort, Serv Med Interne, Niort, France
[15] Ctr Hosp Bretagne Atlantique Vannes, Dept Med Interne, Vannes, France
[16] CHU Grenoble, Serv Nephrol Dialyse & Transplantat, F-38043 Grenoble, France
[17] Univ Lille Nord France, CHU Lille, Ctr Natl Reference Sclerodermie Syst, Hop Claude Huriez,Serv Med Interne, Lille, France
[18] Hop Henri Mondor, AP HP, Ctr Reference Labellise Prise Charge Cytopenies A, Serv Med Interne, F-94010 Creteil, France
[19] Hop Hotel Dieu, Ctr Hosp Univ, Dept Med Interne, Nantes, France
[20] Hop Annecy, Dept Nephrol, Annecy, France
[21] Univ Bourgogne, Ctr Hosp Univ Dijon, Serv Med Interne & Immunol Clin, IFR100, Dijon, France
[22] INSERM, UMR 1098, Besancon, France
[23] Mt Sinai Hosp, Dept Rheumatol, Toronto, ON M5G 1X5, Canada
[24] AP HP, Paris, France
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2014年 / 371卷 / 19期
关键词
ANTIBODY-ASSOCIATED VASCULITIS; LOW-DOSE RITUXIMAB; ANTINEUTROPHIL CYTOPLASMIC AUTOANTIBODIES; RANDOMIZED-TRIAL; WEGENERS-GRANULOMATOSIS; ORAL CYCLOPHOSPHAMIDE; REMISSION-INDUCTION; THERAPY; POLYANGIITIS; METHOTREXATE;
D O I
10.1056/NEJMoa1404231
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
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收藏
页码:1771 / 1780
页数:10
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