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Autologous Bone Marrow Transplantation - Blog Science Connections

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4-Hydroperoxycyclophosphamide and Vincristine<br />

as Ex Vivo <strong>Bone</strong> <strong>Marrow</strong> Treatment for Acute<br />

Leukemia in Second Remission<br />

Leonard J. Horwitz, Miklos L. Auber, Sangeeta Khorana,<br />

Sundar Jagannath, KarelA. Dicke, and Gary Spitzer<br />

A major drawback of autologous bone marrow transplantation (ABMT) in<br />

acute leukemia is the likely presence of occult leukemic cells in the remission<br />

marrow (1). Physical, immunological, and pharmacological procedures or<br />

their combinations have been used in animal models to eliminate this<br />

leukemic cell contamination (2,3).<br />

MATERIALS AND METHODS<br />

The cyclophosphamide derivatives, Asta Z 7557 (mafosfamide) and<br />

4-hydroperoxycyclophosphamide (4-HC), are among the drugs commonly<br />

used for ex vivo chemotherapy (chemopurging) of harvested marrow (4-7).<br />

Clinical studies of ex vivo chemotherapy with 4-HC (40-120 ug/m\) and<br />

ABMT suggest that a small percentage of acute myeloid leukemic (AML)<br />

patients, most of them in second complete remission (CR2), may achieve<br />

long-term disease-free survival. These patients have usually had a previous<br />

complete remission of relatively long duration (18 months or more). Ex vivo<br />

marrow treatment with 4-HC has been less successful for acute lymphoid<br />

143

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