Literature DB >> 34117715

Boosting the oral bioavailability of anticancer drugs through intentional drug-drug interactions.

Eric D Eisenmann1, Zahra Talebi1, Alex Sparreboom1, Sharyn D Baker1.   

Abstract

Oral anticancer drugs suffer from significant variability in pharmacokinetics and pharmacodynamics partially due to limited bioavailability. The limited bioavailability of anticancer drugs is due to both pharmaceutical limitations and physiological barriers. Pharmacokinetic boosting is a strategy to enhance the oral bioavailability of a therapeutic drug by inhibiting physiological barriers through an intentional drug-drug interaction (DDI). This type of strategy has proven effective across several therapeutic indications including anticancer treatment. Pharmacokinetic boosting could improve anticancer drugs lacking or with otherwise unacceptable oral formulations through logistic, economic, pharmacodynamic and pharmacokinetic benefits. Despite these benefits, pharmacokinetic boosting strategies could result in unintended DDIs and are only likely to benefit a limited number of targets. Highlighting this concern, pharmacokinetic boosting has mixed results depending on the boosted drug. While pharmacokinetic boosting did not significantly improve certain drugs, it has resulted in the commercial approval of boosted oral formulations for other drugs. Pharmacokinetic boosting to improve oral anticancer therapy is an expanding area of research that is likely to improve treatment options for cancer patients.
© 2021 Nordic Association for the Publication of BCPT (former Nordic Pharmacological Society).

Entities:  

Keywords:  anticancer; boosting; cancer chemotherapy; drug transporters; drug-drug interactions; drug-metabolising enzymes; pharmacokinetics

Mesh:

Substances:

Year:  2021        PMID: 34117715      PMCID: PMC8665934          DOI: 10.1111/bcpt.13623

Source DB:  PubMed          Journal:  Basic Clin Pharmacol Toxicol        ISSN: 1742-7835            Impact factor:   4.080


  71 in total

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