Long-term follow-up of a randomised controlled trial of azathioprine/methylprednisolone versus cyclophosphamide in patients with proliferative lupus nephritis

被引:45
|
作者
Arends, Suzanne [1 ]
Grootscholten, Cecile [2 ]
Derksen, Ronald H. W. M. [3 ]
Berger, Stefan P. [4 ]
de Sevaux, Ruud G. L. [5 ]
Voskuyl, Alexandre E. [6 ]
Bijl, Marc [1 ]
Berden, Jo H. M. [5 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Rheumatol & Clin Immunol, NL-9700 RB Groningen, Netherlands
[2] Kennemer Gasthuis, Dept Internal Med, Haarlem, Netherlands
[3] Univ Med Ctr Utrecht, Dept Rheumatol & Clin Immunol, Utrecht, Netherlands
[4] Univ Med Ctr, Erasmus MC, Dept Internal Med, Rotterdam, Netherlands
[5] Radboud Univ Nijmegen, Med Ctr, Dept Nephrol, NL-6525 ED Nijmegen, Netherlands
[6] Vrije Univ Amsterdam Med Ctr, Dept Rheumatol, Amsterdam, Netherlands
关键词
AZATHIOPRINE PLUS METHYLPREDNISOLONE; MYCOPHENOLATE-MOFETIL; ORAL CYCLOPHOSPHAMIDE; GLOMERULONEPHRITIS; ERYTHEMATOSUS; PREDICTORS; PREDNISONE; OUTCOMES; THERAPY;
D O I
10.1136/annrheumdis-2011-200384
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives The objectives of this study are to analyse the long-term follow-up of a randomised controlled trial of induction treatment with azathioprine/methylprednisolone (AZA/MP) versus high-dose intravenous cyclophosphamide (ivCY) in patients with proliferative lupus nephritis (LN) and to evaluate the predictive value of clinical, laboratory and renal biopsy parameters regarding renal outcome. Methods 87 patients with biopsy-proven proliferative LN were treated with either AZA/MP (n=37) or ivCY (n=50), both with oral prednisone. After 2 years, renal biopsy was repeated, and all patients continued with AZA/oral prednisone. The primary study end point was sustained doubling of serum creatinine. Secondary end points included renal relapse, end-stage renal disease and mortality. Results After a median follow-up of 9.6 years, no significant differences between AZA/MP versus ivCY groups were found in the proportion of patients with sustained doubling of serum creatinine (n=6 (16%) vs n=4 (8%); p=0.313), end-stage renal disease (n=2 (5%) vs n=2 (4%); p=1.000) or mortality (n=6 (16%) vs n=5 (10%); p=0.388). Renal relapses occurred more often in the AZA/MP group (n=14 (38%) vs n=5 (10%); p=0.002, HR: 4.5). Serum creatinine, proteinuria and immunosuppressive treatment regimens at the last follow-up were comparable. Clinical and laboratory parameters at baseline and after 2 years, and renal biopsy parameters (only) at baseline predicted renal outcome. Conclusion Induction treatment with ivCY was superior to AZA/MP in preventing renal relapses, but other parameters for renal function did not differ. AZA/MP can therefore serve as an alternative in patients with proliferative LN who wish to avoid gonadal toxicity of CY. Several prognostic factors of long-term renal outcome were identified.
引用
收藏
页码:966 / 973
页数:8
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