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Blood, 15 August 2004, Vol. 104, No. 4, pp. 948-955.
Prepublished online as a Blood First Edition Paper on April 15, 2004; DOI 10.1182/blood-2004-02-0593.


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CLINICAL OBSERVATIONS, INTERVENTIONS, AND THERAPEUTIC TRIALS

Blood concentrations of alemtuzumab and antiglobulin responses in patients with chronic lymphocytic leukemia following intravenous or subcutaneous routes of administration

Geoff Hale, Peppy Rebello, Lee R. Brettman, Chris Fegan, Ben Kennedy, Eva Kimby, Mike Leach, Jeanette Lundin, Håkan Mellstedt, Paul Moreton, Andy C. Rawstron, Herman Waldmann, Anders Osterborg, and Peter Hillmen

From the Sir William Dunn School of Pathology, University of Oxford, Oxford, United Kingdom; Millennium Pharmaceuticals, Cambridge, MA; the Department of Haematology, Heartlands Hospital, Birmingham, United Kingdom; the Department of Haematology, Leeds General Infirmary, United Kingdom; the Department of Hematology, Huddinge Hospital, Sweden; the Department of Haematology, Stobhill Hospital, Glasgow, United Kingdom; and the Departments of Hematology and Oncology, Karolinska Hospital, Stockholm, Sweden.

Alemtuzumab is a humanized anti-CD52 antibody licensed for refractory B-cell chronic lymphocytic leukemia (B-CLL), when given intravenously at 30 mg thrice weekly. However, the intravenous route is associated with infusion-related reactions and is inconvenient. We measured blood concentrations in 30 relapsed patients treated with intravenous alemtuzumab and in 20 patients from a previously untreated group who received similar doses subcutaneously. Highest trough samples in the intravenous group were less than 0.5 µg/mL to 18.3 µg/mL (mean 5.4 µg/mL). The cumulative dose required to reach 1.0 µg/mL was 13 mg to 316 mg (mean 90 mg). Higher blood concentrations correlated with the achievement of better clinical responses and minimal residual disease. The highest measured concentrations in the subcutaneous group were similar (0.6 µg/mL to 24.8 µg/mL, mean 5.4 µg/mL). However, the cumulative dose to reach 1.0 µg/mL was higher: 146 mg to 1106 mg (mean 551 mg). No antiglobulin responses were detected in 30 patients given intravenous alemtuzumab whereas 2 of 32 patients given subcutaneous alemtuzumab made substantial anti-idiotype responses. Thus, subcutaneous alemtuzumab achieved concentrations similar to those for intravenous alemtuzumab, although with slightly higher cumulative doses. Subcutaneous alemtuzumab is more convenient and better tolerated but may be associated with some patients forming anti–alemtuzumab antibodies, particularly those patients who were previously untreated.


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