Optimization of Dose Schedules for Chemotherapy of Early Colon Cancer Determined by High-Performance Computer Simulations
                Authored by Chase Cockrell, David E Axelrod
                
                    Date Published: 2019
                
                
                    DOI: 10.1177/1176935118822804
                
                
                    Sponsors:
                    
                        No sponsors listed
                    
                
                
                    Platforms:
                    
                        NetLogo
                        
                
                
                    Model Documentation:
                    
                        Other Narrative
                        
                
                
                    Model Code URLs:
                    
                        https://rucore.libraries.rutgers.edu/rutgers-lib/50717/
                        
                
                Abstract
                Cancer chemotherapy dose schedules are conventionally applied
intermittently, with dose duration of the order of hours, intervals
between doses of days or weeks. and cycles repeated for weeks. The large
number of possible combinations of values of duration. interval, and
lethality has been an impediment to empirically determine the optimal
set of treatment conditions. The purpose of this project was to
determine the set of parameters for duration. interval. and lethality
that would be most effective for treating early colon cancer. An
agent-based computer model that simulated cell proliferation kinetics in
normal human colon crypts was calibrated with measurements of human
biopsy specimens. Mutant cells were simulated as proliferating and
forming an adenoma. or dying if treated with cytotoxic chemotherapy.
Using a high-performance computer. a total of 28 800 different parameter
sets of duration. interval. and lethality were simulated. The effect of
each parameter set on the stability of colon crypts. the time to cure a
crypt of mutant cells. and the accumulated dose was determined. Of the
28 800 parameter sets, 434 parameter sets were effective in curing the
crypts of mutant cells before they could form an adenoma and allowed the
crypt normal cell dynamics to recover to pretreatment levels. A group of
14 similar parameter sets produced a minimal time to cure mutant cells.
A different group of nine similar parameter sets produced the least
accumulated dose. These parameter sets may be considered as candidate
dose schedules to guide clinical trials for early colon cancer.
                
Tags
                
                    Agent-based model
                
                    Computer simulation
                
                    Landscape
                
                    Chemotherapy
                
                    Colon cancer
                
                    Strategies
                
                    Crypt
                
                    Mutants
                
                    Dose schedules
                
                    High-performance computer
                
                    Advanced colorectal-cancer
                
                    Cell-dynamics
                
                    Intermittent