Induction and Maintenance Treatment of Proliferative Lupus Nephritis: A Meta-analysis of Randomized Controlled Trials

被引:87
作者
Henderson, Lorna K. [1 ,2 ]
Masson, Philip [2 ,3 ]
Craig, Jonathan C. [2 ,3 ]
Roberts, Matthew A. [4 ]
Flanc, Robert S. [5 ]
Strippoli, Giovanni F. M. [2 ,3 ,6 ,7 ,8 ]
Webster, Angela C. [2 ,3 ]
机构
[1] Westmead Hosp, Dept Renal Med, Ctr Transplant & Renal Res, Sydney, NSW 2145, Australia
[2] Childrens Hosp, Ctr Kidney Res, Cochrane Renal Grp, Westmead, NSW, Australia
[3] Univ Sydney, Sydney Sch Publ Hlth, Sydney, NSW 2006, Australia
[4] Austin Hlth, Dept Nephrol, Heidelberg, Vic, Australia
[5] Monash Med Ctr, Dept Nephrol, Clayton, Vic 3168, Australia
[6] Mario Negri Sud Consortium, Dept Clin Pharmacol & Epidemiol, Santa Maria Imbaro, Italy
[7] Diaverum Med Sci Off, Lund, Sweden
[8] Univ Bari, Nephrol Sect, Dept Emergency & Organ Transplantat, Bari, Italy
关键词
Lupus nephritis; systemic lupus erythematosus (SLE); proliferative glomerulonephritis; systematic review; meta-analysis; cyclophosphamide (CYC); mycophenolate mofetil (MMF); PULSE INTRAVENOUS CYCLOPHOSPHAMIDE; MYCOPHENOLATE-MOFETIL; COMBINED PREDNISONE; SYSTEMATIC REVIEWS; PLASMA-EXCHANGE; RENAL SURVIVAL; CYCLOSPORINE-A; THERAPY; AZATHIOPRINE; METHYLPREDNISOLONE;
D O I
10.1053/j.ajkd.2012.08.041
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Lupus nephritis accounts for similar to 1% of patients starting dialysis therapy. Treatment regimens combining cyclophosphamide with steroids preserve kidney function but have significant side effects. Newer immunosuppressive agents may have improved toxicity profiles. Study Design: Systematic review and random-effects meta-analysis, searching MEDLINE (1966 to April 2012), EMBASE (1988-2011), and the Cochrane Renal Group Specialised Register. Setting & Population: Patients with biopsy-proven proliferative lupus nephritis (classes III, IV, V+III, and V+IV). Selection Criteria: Randomized controlled trials. Intervention: Immunosuppressive treatment regimens used for induction and maintenance therapy of lupus nephritis. Outcomes: Mortality, renal remission and relapse, doubling of creatinine level, proteinuria, incidence of end-stage kidney disease, ovarian failure, alopecia, leukopenia, infections, diarrhea, vomiting, malignancy, and bladder toxicity. Results: 45 trials (2,559 participants) of induction therapy and 6 (514 participants) of maintenance therapy were included. In induction regimens comparing mycophenolate mofetil (MMF) with intravenous cyclophosphamide, there was no significant difference in mortality (7 studies, 710 patients; risk ratio [RR], 1.02; 95% CI, 0.52-1.98), incidence of end-stage kidney disease (3 studies, 231 patients; RR, 0.71; 95% CI, 0.27-1.84), complete renal remission (6 studies, 686 patients; RR, 1.39; 95% CI, 0.99-1.95), and renal relapse (1 study, 140 patients; RR, 0.97; 95% CI, 0.39-2.44). MMF-treated patients had significantly lower risks of ovarian failure (2 studies, 498 patients; RR, 0.15; 95% CI, 0.03-0.80) and alopecia (2 studies, 522 patients; RR, 0.22; 95% CI, 0.06-0.86). In maintenance therapy comparing azathioprine with MMF, the risk of renal relapse was significantly higher (3 studies, 371 patients; RR, 1.83; 95% CI, 1.24-2.71). Limitations: Heterogeneity in interventions and definitions of remission and lack of long-term outcome reporting. Conclusions: MMF is as effective as cyclophosphamide in achieving remission in lupus nephritis, but is safer, with a lower risk of ovarian failure. MMF is more effective than azathioprine in maintenance therapy for preventing relapse, with no difference in clinically important side effects. Am J Kidney Dis. 61(1):74-87. (C) 2012 by the National Kidney Foundation, Inc.
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收藏
页码:74 / 87
页数:14
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