Long term azathioprine maintenance therapy in ANCA-associated vasculitis: combined results of long-term follow-up data

被引:36
|
作者
de Joode, Anoek A. E. [1 ]
Sanders, Jan Stephan F. [1 ]
Puechal, Xavier [2 ]
Guillevin, Loic P. [3 ]
Hiemstra, Thomas F. [4 ,5 ]
Flossmann, Oliver [6 ]
Rasmussen, Nils [7 ]
Westman, Kerstin [8 ]
Jayne, David R. [5 ,9 ]
Stegeman, Coen A. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Internal Med & Nephrol, Hanzepl 1, NL-9700 RB Groningen, Netherlands
[2] Hop Cochin, Dept Internal Med, Paris, France
[3] Univ Paris 05, Natl Referral Ctr Necrotising Vasculitides & Syst, Paris, France
[4] Univ Cambridge, Dept Internal Med Expt Med & Immunotherapeut, Cambridge, England
[5] Lupus & Vasculitis Unit, Cambridge, England
[6] Royal Berkshire Hosp, Dept Nephrol, Reading, Berks, England
[7] Rigshosp, Dept Ear Nose & Throat, Copenhagen, Denmark
[8] Lund Univ Hosp, Dept Nephrol & Transplantat, Malmo, Sweden
[9] Univ Cambridge, Dept Internal Med & Nephrol, Cambridge, England
关键词
ANCA; PR3; granulomatosis with polyangiitis; vasculitis; azathioprine; maintenance; long-term follow-up; EUVAS; FVSG; ANTIBODY-ASSOCIATED VASCULITIS; WEGENERS-GRANULOMATOSIS; RANDOMIZED-TRIAL; SYSTEMIC VASCULITIS; RENAL INVOLVEMENT; REMISSION; CYCLOPHOSPHAMIDE; INDUCTION; RITUXIMAB; RELAPSE;
D O I
10.1093/rheumatology/kex281
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. We studied whether in ANCA-associated vasculitis patients, duration of AZA maintenance influenced relapse rate during long-term follow-up. Methods. Three hundred and eighty newly diagnosed ANCA-associated vasculitis patients from six European multicentre studies treated with AZA maintenance were included; 58% were male, median age at diagnosis 59.4 years (interquartile range: 48.3-68.2 years); granulomatosis with polyangiitis, n = 236; microscopic polyangiitis, n = 132; or renal limited vasculitis, n = 12. Patients were grouped according to the duration of AZA maintenance after remission induction: 418 months, <= 24 months, <= 36 months, <= 48 months or >48 months. Primary outcome was relapse-free survival at 60 months. Results. During follow-up, 84 first relapses occurred during AZA-maintenance therapy (1 relapse per 117 patient months) and 71 after withdrawal of AZA (1 relapse/113 months). During the first 12 months after withdrawal, 20 relapses occurred (1 relapse/119 months) and 29 relapses >12 months after withdrawal (1 relapse/186 months). Relapse-free survival at 60 months was 65.3% for patients receiving AZA maintenance >18 months after diagnosis vs 55% for those who discontinued maintenance <= 18 months (P = 0.11). Relapse-free survival was associated with induction therapy (i.v. vs oral) and ANCA specificity (PR3-ANCA vs MPO-ANCA/negative). Conclusion. Post hoc analysis of combined trial data suggest that stopping AZA maintenance therapy does not lead to a significant increase in relapse rate and AZA maintenance for more than 18months after diagnosis does not significantly influence relapse-free survival. ANCA specificity has more effect on relapse-free survival than duration of maintenance therapy and should be used to tailor therapy individually.
引用
收藏
页码:1894 / 1901
页数:8
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