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Original Paper
Kidney Blood Press Res 2007;30:124–128
DOI: 10.1159/000101448
Treatment of Lupus Nephritis with
Cyclosporine – An Outcome Analysis
Zuzana Rihova
a
Zdenka Vankova
a
Dita Maixnerova
a
Ctibor Dostal
b
Eva Jancova
a
Eva Honsova
c
Miroslav Merta
a
Romana Rysava
a
Vladimir Tesar
a
a
Nephrology Unit and
b
Institute for Rheumatology, 1st Medical Faculty, Charles University, and
c
Pathology Department, Institute for Clinical and Experimental Medicine, Prague, Czech Republic
Introduction
Renal involvement is common in systemic lupus ery-
thematosus (SLE). An abnormal urinalysis with or with-
out an elevated plasma creatinine concentration is pres-
ent in approximately 50% of patients at the time of diag-
nosis and eventually develops in more than 75% of cases
[1].
Aggressive immunosuppressive therapy should be
employed in patients with proliferative lupus nephritis
(LN) as the risk of progression to end-stage renal disease
is high. Combined treatment with cyclophosphamide
(CYC) and corticosteroids (CS) is generally considered to
be the induction treatment of choice for patients with
WHO class III and IV LN as it improves renal survival.
Prolonged administration of CYC and CS is also associ-
ated with fewer relapses and a decreased risk of renal in-
sufficiency [2] . However, its toxicity, especially in the
light of the relapsing character of SLE with the potential
need of repeated courses of immunosuppressive treat-
ment and the need of non-gonadotoxic therapeutic op-
tion for women in fertile age and in pregnancy, create the
necessity of therapeutic alternatives. Cyclosporine (cy-
closporine A, CsA) is a potent immunosuppressive agent
with a powerful effect on helper T-clonal expansion and
cytotoxic cell function through inhibition of IL-2, IL-3
and IFN- synthesis. CsA had been shown to reduce pro-
Key Words
Cyclosporine Lupus nephritis Systemic Lupus
Erythematosus Disease Activity Index – SLEDAI
Abstract
Background: The optimal therapy for lupus nephritis (LN),
including the role of cyclosporine (CsA), still lacks scientifi-
cally valid clinical experience. We evaluated the efficacy of
CsA in the induction and maintenance treatment of patients
with biopsy-proven LN. Patients and Methods: A total of 31
patients (25 women, 6 men, mean age 29.5 years) were en-
rolled in the study. The majority had proliferative LN. The
mean follow-up was 85.6 8 24.7 months. Results: CsA was
used as first-line treatment in 38.7% of patients and as sec-
ond-line treatment in 61.3% of patients. Complete remission
was achieved in 93.5% of patients. The relapse rate was
45.2%. The mean disease-free interval was 33 months. At the
end of follow-up, a total of 67.9% of the patients were in re-
mission. The treatment led to significant improvement in
proteinuria (p = 0.001) and stabilization of renal function.
Conclusion: CsA might be an appropriate and a less toxic
alternative drug for LN both as a first-choice and rescue
therapy. Copyright © 2007 S. Karger AG, Basel
Received: February 13, 2006
Accepted after revision: March 5, 2007
Published online: March 30, 2007
Zuzana Rihova, MD
Nephrology Unit, 1st Medical Faculty, Charles University
U Nemocnice 2
CZ–128 08 Prague 2 (Czech Republic)
Tel. +420 224 962 663, Fax +420 224 962 696, E-Mail zrihova@centrum.cz
© 2007 S. Karger AG, Basel
1420–4096/07/0302–0124$23.50/0
Accessible online at:
www.karger.com/kbr
Supported by the grant IGA MZ CR 8444-3.