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Randomized Controlled Trial
. 2009 May;20(5):1103-12.
doi: 10.1681/ASN.2008101028. Epub 2009 Apr 15.

Mycophenolate mofetil versus cyclophosphamide for induction treatment of lupus nephritis

Collaborators, Affiliations
Randomized Controlled Trial

Mycophenolate mofetil versus cyclophosphamide for induction treatment of lupus nephritis

Gerald B Appel et al. J Am Soc Nephrol. 2009 May.

Abstract

Recent studies have suggested that mycophenolate mofetil (MMF) may offer advantages over intravenous cyclophosphamide (IVC) for the treatment of lupus nephritis, but these therapies have not been compared in an international randomized, controlled trial. Here, we report the comparison of MMF and IVC as induction treatment for active lupus nephritis in a multinational, two-phase (induction and maintenance) study. We randomly assigned 370 patients with classes III through V lupus nephritis to open-label MMF (target dosage 3 g/d) or IVC (0.5 to 1.0 g/m(2) in monthly pulses) in a 24-wk induction study. Both groups received prednisone, tapered from a maximum starting dosage of 60 mg/d. The primary end point was a prespecified decrease in urine protein/creatinine ratio and stabilization or improvement in serum creatinine. Secondary end points included complete renal remission, systemic disease activity and damage, and safety. Overall, we did not detect a significantly different response rate between the two groups: 104 (56.2%) of 185 patients responded to MMF compared with 98 (53.0%) of 185 to IVC. Secondary end points were also similar between treatment groups. There were nine deaths in the MMF group and five in the IVC group. We did not detect significant differences between the MMF and IVC groups with regard to rates of adverse events, serious adverse events, or infections. Although most patients in both treatment groups experienced clinical improvement, the study did not meet its primary objective of showing that MMF was superior to IVC as induction treatment for lupus nephritis.

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Figures

Figure 1.
Figure 1.
Patient disposition. *Hepatitis/cytomegalovirus infection (n = 16) or other illness (n = 4). ACR, American College of Rheumatology.
Figure 2.
Figure 2.
Response rates of study population and by racial group.

Comment in

References

    1. Waldman M, Appel GB: Update on the treatment of lupus nephritis. Kidney Int 70: 1403–1412, 2006 - PubMed
    1. Font J, Ramos-Casals M, Cervera R, García-Carrasco M, Torras A, Sisó A, Darnell A, Ingelmo M: Cardiovascular risk factors and the long-term outcome of lupus nephritis. QJM 94: 19–26, 2001 - PubMed
    1. Dooley MA, Hogan S, Jennette C, Falk R: Cyclophosphamide therapy for lupus nephritis: Poor renal survival in black Americans. Glomerular Disease Collaborative Network. Kidney Int 51: 1188–1195, 1997 - PubMed
    1. Barr RG, Seliger S, Appel GB, Zuniga R, D'Agati V, Salmon J, Radhakrishnan J: Prognosis in proliferative lupus nephritis: The role of socio-economic status and race/ethnicity. Nephrol Dial Transplant 18: 2039–2046, 2003 - PubMed
    1. Austin HA III, Klippel JH, Balow JE, le Riche NG, Steinberg AD, Plotz PH, Decker JL: Therapy of lupus nephritis: Controlled trial of prednisone and cytotoxic drugs. N Engl J Med 314: 614–619, 1986 - PubMed

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