Rituximab therapy for childhood-onset systemic lupus erythematosus
Objective
To describe the safety and efficacy of rituximab in the treatment of childhood-onset systemic lupus erythematosus (SLE).
Study design
We conducted a French multicenter retrospective study of childhood-onset SLE treated with rituximab.
Results
Eleven girls with severe SLE, including 8 girls with class IV or V lupus nephritis, 2 girls with severe autoimmune cytopenia, and 1 girl with antiprothrombin antibody with severe hemorrhage, were treated with rituximab. The mean age at onset of rituximab treatment was 13.9 years. Patients received 2 to 12 intravenous infusions of rituximab (350-450 mg/m2/infusion), with corticosteroids. Six patients also received different standard immunosuppressive agents, including Cyclophosphamide (2 patients). Remission was achieved in 6 of 8 patients with lupus nephritis and in the 2 patients with autoimmune cytopenia. Steroid therapy was tapered in 5 patients who responded to treatment, and low-dose prednisone treatment was maintained in 1 patient. The mean follow-up period was 13.2 months (range, 6-26 months), and remission lasted in all who patients who responded to treatment, except 1 patient who was successfully retreated with a second course of rituximab. Anti-double-stranded DNA antibody levels decreased in 6 of 11 patients, and anticardiolipin antibody levels decreased in 3 of 4 patients. Severe adverse events developed in 5 patients. Effective depletion of peripheral blood B cells was observed in 7 of 8 patients who were examined, and this paralleled the remission.
Conclusion
Rituximab may be an effective co-therapy; however, further investigations are required because severe adverse events occurred in 45% of the patients in this study.
Abbreviations:
ACR,
American College of Rheumatology
,
AIHA,
Autoimmune hemolytic anemia
,
AITP,
Autoimmune thrombocytopenia
,
Anti-dsDNA
,
Anti-double-stranded DNA
,
AZA,
Azathioprine
,
CSA,
Ciclosporine
,
CYC,
Cyclophosphamide
,
IG,
Immunoglobulin
,
IGIV,
Intravenous immunoglobulins
,
MMF,
Mycophenolate Mofetyl
,
MP,
Mercaptopurine
,
MTX,
Methotrexate
,
PRED,
Prednisone
,
SLE,
Systemic lupus erythematosus
,
WHO,
World Health Organization
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Supported by a grant from the Association française pour le syndrome d’Evans.
PII: S0022-3476(06)00069-2
doi:10.1016/j.jpeds.2006.01.041
© 2006 Elsevier Inc. All rights reserved.
Refers to article:
- Targeting B cells in the treatment of childhood-onset systemic lupus erythematosus
Refers to erratum:
- Correction
