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- W2260984915 endingPage "1904" @default.
- W2260984915 startingPage "1891" @default.
- W2260984915 abstract "The existing tumor heterogeneity and the complexity of cancer cell biology critically demand powerful translational tools with which to support interdisciplinary efforts aiming to advance personalized cancer medicine decisions in drug development and clinical practice. The development of physiologically based pharmacokinetic (PBPK) models to predict the effects of drugs in the body facilitates the clinical translation of genomic knowledge and the implementation of in vivo pharmacology experience with pharmacogenomics. Such a direction unequivocally empowers our capacity to also make personalized drug dosage scheme decisions for drugs, including molecularly targeted agents and innovative nanoformulations, i.e. in establishing pharmacotyping in prescription. In this way, the applicability of PBPK models to guide individualized cancer therapeutic decisions of broad clinical utility in nanomedicine in real-time and in a cost-affordable manner will be discussed. The latter will be presented by emphasizing the need for combined efforts within the scientific borderlines of genomics with nanotechnology to ensure major benefits and productivity for nanomedicine and personalized medicine interventions." @default.
- W2260984915 created "2016-06-24" @default.
- W2260984915 creator A5016619825 @default.
- W2260984915 creator A5018410921 @default.
- W2260984915 creator A5030500286 @default.
- W2260984915 creator A5056513069 @default.
- W2260984915 creator A5091628026 @default.
- W2260984915 date "2016-01-18" @default.
- W2260984915 modified "2023-10-17" @default.
- W2260984915 title "Enabling personalized cancer medicine decisions: The challenging pharmacological approach of PBPK models for nanomedicine and pharmacogenomics (Review)" @default.
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