F-ara-A pharmacokinetics during reduced-intensity conditioning therapy with fludarabine and busulfan

Author:

Bonin M,Pursche S,Bergeman T,Leopold T,Illmer T,Ehninger G,Schleyer E,Bornhauser M

Publisher

Springer Science and Business Media LLC

Subject

Transplantation,Hematology

Reference19 articles.

1. Chun HG, Leyland-Jones BR, Caryk SM, Hoth DF . Central nervous system toxicity of fludarabine phosphate. Cancer Treat Rep 1986; 70: 1225–1228.

2. Gandhi V, Plunkett W . Cellular and clinical pharmacology of fludarabine. Clin Pharmacokinet 2002; 41: 93–103.

3. Ross SR, McTavish D, Faulds D . Fludarabine. A review of its pharmacological properties and therapeutic potential in malignancy. Drugs 1993; 45: 737–759.

4. Gandhi V, Estey E, Du M, Keating MJ, Plunkett W . Minimum dose of fludarabine for the maximal modulation of 1-beta-D-arabinofuranosylcytosine triphosphate in human leukemia blasts during therapy. Clin Cancer Res 1997; 3: 1539–1545.

5. Gandhi V, Robertson LE, Keating MJ, Plunkett W . Combination of fludarabine and arabinosylcytosine for treatment of chronic lymphocytic leukemia: clinical efficacy and modulation of arabinosylcytosine pharmacology. Cancer Chemother Pharmacol 1994; 34: 30–36.

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