Definition
Is the prodrug of 9-β-d-arabinosyl-2-fluoroadenine (F-ara-A), a synthetic halogen-substituted analogue of deoxyadenosine. Fludarabine and the two other related compounds cladribine (2-chloro-2′-deoxyadenosine) and pentostatin (2′-deoxycoformycin) are collectively referred to as purine analogues, although pentostatin is not actually an analogue, but an inhibitor of adenosine deaminase. Fludarabine is widely used in the treatment of indolent lymphoproliferative malignancies, acute myeloid leukemia, and as a part of the conditioning regimen for non-myeloablative allogeneic stem cell transplantation.
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Clinical and Cellular Pharmacology
The development of fludarabine stemmed from the success of the cytosine analogue cytarabine(ara-C) in the treatment of acute myeloid leukemia. A similar adenine analogue, Ara-A (vidarabine), was a successful antiviral agent...
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Gandhi V, Plunkett W (2002) Cellular and clinical pharmacology of fludarabine. Clin Phamacokinet 41:93–103
Pettitt A (2003) Mechanism of action of purine analogues in chronic lymphocytic leukemia. Brit J Haematol 121:692–702
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© 2011 Springer-Verlag Berlin Heidelberg
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Tam, C.S., Seymour, J.F. (2011). Fludarabine. In: Schwab, M. (eds) Encyclopedia of Cancer. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-16483-5_2211
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DOI: https://doi.org/10.1007/978-3-642-16483-5_2211
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Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-16482-8
Online ISBN: 978-3-642-16483-5
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