One year follow-up of children and adolescents with chronic immune thrombocytopenic purpura (ITP) treated with rituximab. Academic Article uri icon

Overview

abstract

  • BACKGROUND: We previously showed in a prospective study that rituximab appears to be effective in some children and adolescents with severe chronic immune thrombocytopenia. Eleven of 36 patients achieved and maintained platelet counts over 50,000/mm(3) within the first 12 weeks. These patients were followed for the next year. METHODS: Platelet counts were monitored monthly and all subsequent bleeding manifestations and need for further treatment was noted. RESULTS: Eight of the 11 initial responders maintained a platelet count over 150,000/mm(3) without further treatment intervention. Three patients had a late relapse. One initial non-responder achieved a remission after 16 weeks, and two additional patients maintained platelet counts around 50,000/mm(3) without the need for further intervention. CONCLUSIONS: Rituximab resulted in sustained efficacy with platelet counts of 50,000/mm(3) or higher in 11 of 36 patients (31%).

publication date

  • February 1, 2009

Research

keywords

  • Antibodies, Monoclonal
  • Purpura, Thrombocytopenic, Idiopathic

Identity

PubMed Central ID

  • PMC5752113

Scopus Document Identifier

  • 59449095901

Digital Object Identifier (DOI)

  • 10.1002/pbc.21757

PubMed ID

  • 18937333

Additional Document Info

volume

  • 52

issue

  • 2