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Review
. 2010 May 28;70(8):1013-9.
doi: 10.2165/11203850-000000000-00000.

Ofatumumab

Affiliations
Review

Ofatumumab

Mark Sanford et al. Drugs. .

Abstract

Ofatumumab is a fully human anti-CD20 monoclonal antibody that induces antibody-dependent cell-mediated cytotoxicity and complement-dependent cytotoxicity in CD20-expressing B lymphocytes. Ofatumumab is highly potent in lysing B cells, and this appears to stem from its binding site on the short extracellular loop of the target CD20 protein and its slow release from the target molecule. In a pivotal, noncomparative study in patients with fludarabine- and alemtuzumab-refractory chronic lymphocytic leukaemia (CLL), ofatumumab induced objective responses in 58% (99% CI 40, 74) of patients, which met a prespecified superiority criterion. The median duration of response was 7.1 months. The median progression-free survival was 5.7 months and the median overall survival was 13.7 months. In patients with fludarabine- and alemtuzumab-refractory CLL, infections and neutropenia were the most frequent treatment-related adverse events (all grades) that occurred during ofatumumab treatment; infections that commenced during treatment led to death in five patients (8%).

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References

    1. J Clin Oncol. 2010 Apr 1;28(10):1749-55 - PubMed
    1. J Immunol. 2006 Jul 1;177(1):362-71 - PubMed
    1. Leukemia. 2009 Mar;23(3):457-66 - PubMed
    1. Cancer. 2009 Jul 1;115(13):2824-36 - PubMed
    1. Mayo Clin Proc. 2004 Mar;79(3):388-98 - PubMed

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