Authors:
VM Daryani, YT Patel, M Tagen, DC Turner, AM Carcaboso, JM Atkinson, A Gajjar, RJ Gilbertson, KD Wright, CF Stewart
Journal name: 
CPT Pharmacometrics Syst Pharmacol
Citation info: 
5(4):211-221
Abstract: 
We previously investigated novel therapies for pediatric ependymoma and found 5-fluorouracil (5-FU) i.v. bolus increased survival in a representative mouse model. However, without a quantitative framework to derive clinical dosing recommendations, we devised a translational pharmacokinetic-pharmacodynamic (PK-PD) modeling and simulation approach. Results from our preclinical PK-PD model suggested tumor concentrations exceeded the 1-hour target exposure (in vitro IC90), leading to tumor growth delay and increased survival. Using an adult population PK model, we scaled our preclinical PK-PD model to children. To select a 5-FU dosage for our clinical trial in children with ependymoma, we simulated various 5-FU dosages for tumor exposures and tumor growth inhibition, as well as considering tolerability to bolus 5-FU administration. We developed a pediatric population PK model of bolus 5-FU and simulated tumor exposures for our patients. Simulations for tumor concentrations indicated that all patients would be above the 1-hour target exposure for antitumor effect.
DOI: 
http://doi.org/10.1002/psp4.12075
Research group: 
Gilbertson Group
E-pub date: 
01 Apr 2016