Model Comparison and Uncertainty Quantification in Tumor Growth

Abstract

Mathematical and computational modeling have been increasingly applied in many areas of cancer research, aiming to improve the understanding of tumorigenic mechanisms and to suggest more effective therapy protocols. The mathematical description of the tumor growth dynamics is often made using the exponential, logistic, and Gompertz models. However, recent literature has suggested that the Allee effect may play an important role in the early stages of tumor dynamics, including cancer relapse and metastasis. For a model to provide reliable predictions, it is necessary to have a rigorous evaluation of the uncertainty inherent in the modeling process. In this work, our main objective is to show how a model framework that integrates sensitivity analysis, model calibration, and model selection techniques can improve and systematically characterize model and data uncertainties. We investigate five distinct models with different complexities, which encompass the exponential, logistic, Gompertz, and weak and strong Allee effects dynamics. Using tumor growth data published in the literature, we perform a global sensitivity analysis, apply a Bayesian framework for parameter inference, evaluate the associated sensitivity matrices, and use different information criteria for model selection (First- and Second-Order Akaike Information Criteria and Bayesian Information Criterion). We show that such a wider methodology allows having a more detailed picture of each model assumption and uncertainty, calibration reliability, ultimately improving tumor mathematical description. The used in vivo data suggested the existence of both a competitive effect among tumor cells and a weak Allee effect in the growth dynamics. The proposed model framework highlights the need for more detailed experimental studies on the influence of the Allee effect on the analyzed cancer scenario.

SINDy-SA framework: enhancing nonlinear system identification with sensitivity analysis

“…In our next application, we consider the logistic growth model, previously calibrated using 14 tumor volume (in mm ) data points from the breast cancer growth (GI-101A xenografts) in athymic mice, distributed over 114 days [ 24 ]. By denoting x ( t ) as the tumor volume at time t , the evolution of the tumor volume over time, days, is then given by: …”