Practical Understanding of Cancer Model Identifiability in Clinical Applications

被引:10
作者
Phan, Tin [1 ,2 ]
Bennett, Justin [2 ,3 ]
Patten, Taylor [2 ,4 ]
机构
[1] Los Alamos Natl Lab, Theoret Biol & Biophys, Los Alamos, NM 87544 USA
[2] Arizona State Univ, Sch Math & Stat Sci, Tempe, AZ 85281 USA
[3] Johns Hopkins Univ, Dept Appl Math & Stat, Baltimore, MD 21218 USA
[4] Midwestern Univ, Arizona Coll Osteopath Med, Glendale, AZ 85308 USA
来源
LIFE-BASEL | 2023年 / 13卷 / 02期
关键词
observing-system simulation experiment; mathematical oncology; computational oncology; clinical application; model identifiability; prostate cancer; precision treatment; mathematical model; PROSTATE-CANCER; ANDROGEN SUPPRESSION; DATA ASSIMILATION; DYNAMICS; PARAMETERS; RESISTANCE; THERAPY; SYSTEMS; GROWTH; CELLS;
D O I
10.3390/life13020410
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mathematical models are a core component in the foundation of cancer theory and have been developed as clinical tools in precision medicine. Modeling studies for clinical applications often assume an individual's characteristics can be represented as parameters in a model and are used to explain, predict, and optimize treatment outcomes. However, this approach relies on the identifiability of the underlying mathematical models. In this study, we build on the framework of an observing-system simulation experiment to study the identifiability of several models of cancer growth, focusing on the prognostic parameters of each model. Our results demonstrate that the frequency of data collection, the types of data, such as cancer proxy, and the accuracy of measurements all play crucial roles in determining the identifiability of the model. We also found that highly accurate data can allow for reasonably accurate estimates of some parameters, which may be the key to achieving model identifiability in practice. As more complex models required more data for identification, our results support the idea of using models with a clear mechanism that tracks disease progression in clinical settings. For such a model, the subset of model parameters associated with disease progression naturally minimizes the required data for model identifiability.
引用
收藏
页数:18
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