期刊
EUROPEAN JOURNAL OF CANCER
卷 67, 期 -, 页码 213-222出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.ejca.2016.07.024
关键词
Heterogeneity of patient responses; Clinical trials; Mathematical model; Stratification; Treatment schedule optimisation
类别
资金
- Moffitt Cancer Center PS-OC NIH/NCI [1U54CA143970-01, R01 CA161107-01]
- NCI Comprehensive Cancer Center [P30-CA076292]
- PSOC NIH/NCI [1U54CA193489-01A1, P50 CA168536]
Background: One of major issues in clinical trials in oncology is their high failure rate, despite the fact that the trials were designed based on the data from successful equivalent preclinical studies. This is in part due to the intrinsic homogeneity of preclinical model systems and the contrasting heterogeneity of actual patient responses. Methods: We present a mathematical model-driven framework, phase i (virtual/imaginary) trials, that integrates the heterogeneity of actual patient responses and preclinical studies through a cohort of virtual patients. The framework includes an experimentally calibrated mathematical model, a cohort of heterogeneous virtual patients, an assessment of stratification factors, and treatment optimisation. We show the detailed process through the lens of melanoma combination therapy (chemotherapy and an AKT inhibitor), using both preclinical and clinical data. Results: The mathematical model predicts melanoma treatment response and resistance to mono and combination therapies and was calibrated and then validated with in vitro experimental data. The validated model and a genetic algorithm were used to generate virtual patients whose tumour volume responses to the combination therapy matched statistically the actual heterogeneous patient responses in the clinical trial. Analyses on simulated cohorts revealed key model parameters such as a tumour volume doubling rate and a therapy induced phenotypic switch rate that may have clinical correlates. Finally, our approach predicts optimal AKT inhibitor scheduling suggesting more effective but less toxic treatment strategies. Conclusion: Our proposed computational framework to implement phase i trials in cancer can readily capture observed heterogeneous clinical outcomes and predict patient survival. Importantly, phase i trials can be used to optimise future clinical trial design. (C) 2016 Elsevier Ltd. All rights reserved.
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