Pharmacogenetics, enzyme probes and therapeutic drug monitoring as potential tools for individualizing taxane therapy.

TitlePharmacogenetics, enzyme probes and therapeutic drug monitoring as potential tools for individualizing taxane therapy.
Publication TypeJournal Article
Year of Publication2013
AuthorsKrens, Stefanie D., Howard L. McLeod, and Daniel L. Hertz
JournalPharmacogenomics
Volume14
Issue5
Pagination555-74
Date Published2013 Apr
ISSN1744-8042
KeywordsAntineoplastic Agents, Breast Neoplasms, Bridged-Ring Compounds, Docetaxel, Drug Monitoring, Female, Humans, Neoplasms, Paclitaxel, Pharmacogenetics, Precision Medicine, Taxoids
Abstract

The taxanes are a class of chemotherapeutic agents that are widely used in the treatment of various solid tumors. Although taxanes are highly effective in cancer treatment, their use is associated with serious complications attributable to large interindividual variability in pharmacokinetics and a narrow therapeutic window. Unpredictable toxicity occurrence necessitates close patient monitoring while on therapy and adverse effects frequently require decreasing, delaying or even discontinuing taxane treatment. Currently, taxane dosing is based primarily on body surface area, ignoring other factors that are known to dictate variability in pharmacokinetics or outcome. This article discusses three potential strategies for individualizing taxane treatment based on patient information that can be collected before or during care. The clinical implementation of pharmacogenetics, enzyme probes or therapeutic drug monitoring could enable clinicians to personalize taxane treatment to enhance efficacy and/or limit toxicity.

DOI10.2217/pgs.13.33
Alternate JournalPharmacogenomics
Original PublicationPharmacogenetics, enzyme probes and therapeutic drug monitoring as potential tools for individualizing taxane therapy.
PubMed ID23556452
PubMed Central IDPMC3975654
Grant ListP01 CA142538 / CA / NCI NIH HHS / United States
UL1 RR025747 / RR / NCRR NIH HHS / United States
UL1RR025747 / RR / NCRR NIH HHS / United States
P01CA142538 / CA / NCI NIH HHS / United States
Project: