Abstract
Event free survival in children with Acute Myeloid Leukemia (AML) remains low at approximately 50%, and more effective therapy is urgently needed. Alemtuzumab is an anti-CD52 humanized antibody with activity in Chronic Lymphocytic Leukemia. In adults with AML, CD52 was expressed in 36% of patients. Alemtuzumab treatment in relapsed adult AML patients resulted in complete response without platelet recovery (CRp) in 2/9 (22%), reduction of marrow blasts in 1/9 (11%) and reduction of peripheral blasts in 5/9 (56%) (
Cytogenetic Risk Group . | Low Risk: t(8;21) or Inv(16)/t(16;16) . | Intermediate Risk . | High Risk: −7 or -5/5q- . | Down Syndrome . |
---|---|---|---|---|
CD52 positive | 7 | 9 | 2 | 1 |
CD52 negative | 2 | 13 | 3 | 4 |
Cytogenetic Risk Group . | Low Risk: t(8;21) or Inv(16)/t(16;16) . | Intermediate Risk . | High Risk: −7 or -5/5q- . | Down Syndrome . |
---|---|---|---|---|
CD52 positive | 7 | 9 | 2 | 1 |
CD52 negative | 2 | 13 | 3 | 4 |
More low-risk patients were CD52 positive than negative, but the reverse was true for patients with Down syndrome. Age, gender, FAB subtype or presenting white blood cell count did not correlate with CD52 expression. Event free survival and overall survival were similar in CD52 positive and negative patients. In summary, CD52 is expressed in almost half of children with AML. The activity of single agent Alemtuzumab in adults with AML suggests that this agent should be evaluated to treat CD52-positive pediatric AML patients in combination with chemotherapy.
Author notes
Disclosure: No relevant conflicts of interest to declare.
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