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NDT Advance Access originally published online on January 29, 2009
Nephrology Dialysis Transplantation 2009 24(7):2157-2160; doi:10.1093/ndt/gfp002
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© The Author [2009]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org



Rituximab and mycophenolate mofetil for relapsing proliferative lupus nephritis: a long-term prospective study

John N. Boletis1, Smaragde Marinaki1, Chryssanthe Skalioti1, Sofia S. Lionaki1, Aliki Iniotaki2 and Petros P. Sfikakis3

1 Nephrology Department, Laikon Hospital 2 Immunology Department, Gennimatas Hospital 3 First Department of Propedeutic and Internal Medicine, Athens University Medical School, Athens, Greece

Correspondence and offprint requests to: John N. Boletis; E-mail: laikneph{at}laiko.gr



  Abstract

Background. Subsequent to cyclophosphamide-based induction therapy of lupus nephritis, and despite maintenance chronic immunosuppressive treatment, many patients experience relapses.

Methods. This prospective, observational study included 10 women with biopsy-proven relapse of proliferative lupus nephritis occurring during maintenance with mycophenolate mofetil (MMF) or azathioprine. The long-term outcome after a single course of the B-cell depleting anti-CD20 antibody rituximab (4 weekly infusions of 375 mg/m2), combined with daily MMF (2 g) and prednisolone (0.5 mg/ kg/day for 4 weeks, tapered thereafter) is presented.

Results. While renal function was not severely impaired at baseline, partial remission (>50% improvement in all abnormal renal parameters) was achieved in eight patients at a median of 3.5 months. In seven patients, with 24-h urinary protein of 2.5 ± 1.1 g (mean ± SD), complete remission, associated with increases in serum complement levels and decreases in anti-dsDNA titres, was subsequently established (normal serum creatinine/albumin levels, inactive urine sediment and 24-h urinary protein <0.5 g). Complete nephritis remission was sustained at the follow-up end (median of 38 months) in six patients. Combination treatment was well tolerated.

Conclusions. The efficacy of this low-toxicity combination was particularly evident in patients with subnephrotic proteinuria due to proliferative lupus nephritis relapse. Controlled trials to define the role of rituximab/MMF in this condition are warranted.

Keywords: CD20; mycophenolate mofetil; nephritis; relapse; rituximab; systemic lupus erythematosus

Received for publication: 16.10.08
Accepted in revised form: 31.12.08


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