Bertil Glader

Publication Details

  • Prospective phase 1/2 study of rituximab in childhood and adolescent chronic immune thrombocytopenic purpura BLOOD Bennett, C. M., Rogers, Z. R., Kinnamon, D. D., Bussel, J. B., Mahoney, D. H., Abshire, T. C., Sawaf, H., Moore, T. B., Loh, M. L., Glader, B. E., McCarthy, M. C., Mueller, B. U., Olson, T. A., Lorenzana, A. N., Mentzer, W. C., Buchanan, G. R., Feldman, H. A., Neufeld, E. J. 2006; 107 (7): 2639-2642


    We assessed safety and efficacy of rituximab in a prospective study of 36 patients, age 2.6 to 18.3 years, with severe chronic immune thrombocytopenic purpura (ITP). The primary outcome of sustained platelets above 50 x 10(9)/L (50,000/mm3) during 4 consecutive weeks, starting in weeks 9 to 12, was achieved by 11 of 36 patients (31%, confidence interval [CI], 16% to 48%). Median response time was 1 week (range, 1 to 7 weeks). Attainment of the primary outcome was not associated with age, prior pharmacologic responses, prior splenectomy, ITP duration, screening platelet count, refractoriness, or IgM reduction. First-dose, infusion-related toxicity was common (47%) despite premedication. Significant drug-related toxicities included third-dose hypotension (n = 1) and serum sickness (n = 2). Peripheral B cells were depleted in all subjects. IgM decreased 3.4% per week, but IgG did not significantly decrease. Rituximab was well tolerated, with manageable infusion-related side effects, but 6% of subjects developed serum sickness. Rituximab is beneficial for some pediatric patients with severe, chronic ITP.

    View details for Web of Science ID 000236656900019

    View details for PubMedID 16352811

Stanford Medicine Resources:

Footer Links: