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Alemtuzumab toxicity

NK cells, monocytes, macrophages, and a small population of granulocytes. Currently, alemtuzumab is approved for the treatment of -cell chronic lymphocytic leukemia in patients who have been treated with alkylating agents and have failed fludarabine therapy. Alemtuzumab appears to deplete leukemic and normal cells by direct antibody-dependent lysis. Patients receiving this antibody become lymphopenic and may also become neutropenic, anemic, and thrombocytopenic. As a result patients should be closely monitored for opportunistic infections and hematologic toxicity. [Pg.1197]

Alemtuzumab ADCC CDC apoptosis Escalation 3, 10, 30 mg/m IV 3 times per week followed by 30 mg/m 3 times per week for 4 to 12 weeks Infusion-related toxicity, T-cell depletion with increased infection hematopoietic suppression pancytopenia... [Pg.903]

Alemtuzumab CD52 B-cell chronic lymphocytic leukemia Infections, hematologic toxicity, infusion reactions, hypersensitivity... [Pg.455]


See other pages where Alemtuzumab toxicity is mentioned: [Pg.1420]    [Pg.512]    [Pg.218]    [Pg.1349]    [Pg.87]    [Pg.958]    [Pg.2521]    [Pg.2549]   
See also in sourсe #XX -- [ Pg.901 , Pg.903 ]




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Alemtuzumab

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