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Review
. 2009 Dec;10(12):1897-903.
doi: 10.2217/pgs.09.134.

Drug focus: Pharmacogenetic studies related to cyclophosphamide-based therapy

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Review

Drug focus: Pharmacogenetic studies related to cyclophosphamide-based therapy

Navin Pinto et al. Pharmacogenomics. 2009 Dec.

Abstract

Cyclophosphamide is a cornerstone in the treatment of many pediatric and adult malignancies, as well as in the treatment of refractory autoimmune conditions. Genetic factors are thought to play a role in the interindividual variation in both response and toxicities associated with cyclophosphamide-based therapies. This drug focus reviews the most compelling studies conducted on the pharmacogenetics of cyclophosphamide-based therapies. Broader pharmacogenomic studies are needed and may reveal additional factors important in susceptibility to toxicity and/or response to therapy.

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References

    1. Colvin OM. An overview of cyclophosphamide development and clinical applications. Curr Pharm Des. 1999;5(8):555–560. - PubMed
    1. Ludeman SM. The chemistry of the metabolites of cyclophosphamide. Curr Pharm Des. 1999;5(8):627–643. - PubMed
    1. Cox PJ. Cyclophosphamide cystitis – identification of acrolein as the causative agent. Biochem Pharmacol. 1979;28(13):2045–2049. - PubMed
    1. Parekh HK, Sladek NE. NADPH-dependent enzyme-catalyzed reduction of aldophosphamide, the pivotal metabolite of cyclophosphamide. Biochem Pharmacol. 1993;46(6):1043–1052. - PubMed
    1. Hayes JD, Pulford DJ. The glutathione S-transferase supergene family: regulation of GST and the contribution of the isoenzymes to cancer chemoprotection and drug resistance. Crit Rev Biochem Mol Biol. 1995;30(6):445–600. - PubMed

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