Premium
A pharmacokinetic–pharmacodynamic model predicting tumour growth inhibition after intermittent administration with the mTOR kinase inhibitor AZD8055
Author(s) -
Yates James W T,
Holt Sarah V,
Logie Armelle,
Payne Kirsty,
Woods Karen,
Wilkinson Robert W,
Davies Barry R,
Guichard Sylvie M
Publication year - 2017
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1111/bph.13886
Subject(s) - pharmacodynamics , pharmacokinetics , pharmacology , medicine , in vivo , dosing , pi3k/akt/mtor pathway , ex vivo , chemistry , biology , signal transduction , biochemistry , microbiology and biotechnology
Background and Purpose AZD8055 is a potent orally available mTOR kinase inhibitor with in vitro and in vivo antitumour activity against a range of tumour types. Preclinical studies showed that AZD8055 induced a dose‐dependent pharmacodynamic effect in xenograft models in vivo , but a lack of understanding of the relative contributions of the maximum inhibition of the biomarkers and the duration of inhibition to the antitumour effect, limited the rational design of experiments to optimize the dose and schedules of treatment. Experimental Approach In this study, a mathematical modelling approach was developed to relate pharmacodynamics and antitumour activity using preclinical data generated in mice bearing U87‐MG xenografts. Key Results Refinement and validation of the model was carried out in a panel of additional human tumour xenograft models with different growth rates and different sensitivity to AZD8055 (from partial growth inhibition to regression). Finally, the model was applied to accurately predict the efficacy of high, intermittent dosing schedules of AZD8055. Conclusions and Implications Overall, this new model linking pharmacokinetics, pharmacodynamic biomarkers and efficacy across several tumour xenografts with different sensitivity to AZD8055 was able to identify the optimal dose and route of administration to maximize the antitumour efficacy in preclinical models and its potential for translation into man.