Abstract
The safety and efficacy of rituximab have been retrospectively assessed in 17 children with Evans syndrome. Patients received 4 or 3 weekly doses of rituximab (375 mg/m(2) per dose) associated with prednisone, alone (14 patients) or associated with other immunosuppressive drugs. Complete or partial remission of at least one cytopenia was achieved in 13 out of the 17 patients (76%), and lasted in 11 of them with a mean follow-up of 2.4 years (range 0.5-7 years). Steroid therapy was stopped or tapered at 50-100% of the baseline dosage in all long-term responders. Moderate side effects and infection occurred only in 4 and 1 children respectively.
Publication types
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Multicenter Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Adolescent
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Anemia, Hemolytic, Autoimmune / complications
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Anemia, Hemolytic, Autoimmune / drug therapy*
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Anemia, Hemolytic, Autoimmune / mortality
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Antibodies, Monoclonal / administration & dosage*
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Antibodies, Monoclonal / adverse effects
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Antibodies, Monoclonal, Murine-Derived
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Child
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Child, Preschool
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Disease-Free Survival
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Female
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Follow-Up Studies
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France
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Humans
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Immunologic Factors / administration & dosage*
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Immunologic Factors / adverse effects
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Infant
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Infections / chemically induced
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Infections / mortality
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Male
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Prednisolone / administration & dosage
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Prednisolone / adverse effects
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Purpura, Thrombocytopenic, Idiopathic / complications
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Purpura, Thrombocytopenic, Idiopathic / drug therapy*
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Purpura, Thrombocytopenic, Idiopathic / mortality
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Registries
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Remission Induction
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Rituximab
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Survival Rate
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Syndrome
Substances
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Antibodies, Monoclonal
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Antibodies, Monoclonal, Murine-Derived
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Immunologic Factors
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Rituximab
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Prednisolone