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   <subfield code="a">Low rate of long-lasting remissions after successful treatment of immune thrombocytopenic purpura with rituximab</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Christof Schweizer, Frederic Reu, Anthony Ho, Manfred Hensel]</subfield>
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   <subfield code="a">Idiopathic thrombocytopenic purpura (ITP), also known as immune thrombocytopenic purpura, is thought to be caused primarily by the production of autoantibodies directed against platelet surface glycoproteins. Treatment of an acute ITP episode can be difficult, and relapses are common. Recent studies have shown that the anti-CD20 antibody rituximab is effective in the treatment of relapsed and refractory patients. We report the results of a retrospective analysis of rituximab treatment in 14 patients with immune thrombocytopenic purpura. Nine of these patients had a refractory disease, and five patients had a relapse of the thrombocytopenia. The median time since last treatment was 10days (range 1-470days). All patients were previously treated with one to seven different regimens, and four had undergone splenectomy. Rituximab was administered at the standard dose of 375mg/m2 once per week with a median of 4 infusions (range 2-4). The overall response rate was 64%; 7 of 14 patients (50%) achieved a complete remission (platelet levels &gt; 100 × 109/l), 2 of 14 patients (14%) had a partial remission (platelets &gt; 50 × 109/l), and 5 patients did not respond. The median time to response was 2weeks (range 1-4) after the first infusion. Responding patients stayed in remission for a median period of 8weeks (range 10days-36months). Three patients (21%) remained in remission after 26 to 156weeks of follow-up. All of the four splenectomized patients achieved a complete remission after rituximab therapy, and two of them are still in remission after 26 and 156weeks observation. Our data confirm that rituximab is well tolerated and effective in refractory and relapsed immune thrombocytopenias; however, response duration was short, and only about one fifth of our patients enjoyed a long-lasting remission.</subfield>
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   <subfield code="a">ITP</subfield>
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   <subfield code="a">Idiopathic thrombocytopenic purpura</subfield>
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   <subfield code="a">Schweizer</subfield>
   <subfield code="D">Christof</subfield>
   <subfield code="u">Department of Internal Medicine V, Haematology, Oncology and Rheumatology, University of Heidelberg, Im Neuenheimer Feld 410, 69120, Heidelberg, Germany</subfield>
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   <subfield code="a">Reu</subfield>
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   <subfield code="a">Ho</subfield>
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   <subfield code="t">Annals of Hematology</subfield>
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