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Classical Mathematical Models for Description and Prediction of Experimental Tumor Growth

Overview of attention for article published in PLoS Computational Biology, August 2014
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Title
Classical Mathematical Models for Description and Prediction of Experimental Tumor Growth
Published in
PLoS Computational Biology, August 2014
DOI 10.1371/journal.pcbi.1003800
Pubmed ID
Authors

Sébastien Benzekry, Clare Lamont, Afshin Beheshti, Amanda Tracz, John M. L. Ebos, Lynn Hlatky, Philip Hahnfeldt

Abstract

Despite internal complexity, tumor growth kinetics follow relatively simple laws that can be expressed as mathematical models. To explore this further, quantitative analysis of the most classical of these were performed. The models were assessed against data from two in vivo experimental systems: an ectopic syngeneic tumor (Lewis lung carcinoma) and an orthotopically xenografted human breast carcinoma. The goals were threefold: 1) to determine a statistical model for description of the measurement error, 2) to establish the descriptive power of each model, using several goodness-of-fit metrics and a study of parametric identifiability, and 3) to assess the models' ability to forecast future tumor growth. The models included in the study comprised the exponential, exponential-linear, power law, Gompertz, logistic, generalized logistic, von Bertalanffy and a model with dynamic carrying capacity. For the breast data, the dynamics were best captured by the Gompertz and exponential-linear models. The latter also exhibited the highest predictive power, with excellent prediction scores (≥80%) extending out as far as 12 days in the future. For the lung data, the Gompertz and power law models provided the most parsimonious and parametrically identifiable description. However, not one of the models was able to achieve a substantial prediction rate (≥70%) beyond the next day data point. In this context, adjunction of a priori information on the parameter distribution led to considerable improvement. For instance, forecast success rates went from 14.9% to 62.7% when using the power law model to predict the full future tumor growth curves, using just three data points. These results not only have important implications for biological theories of tumor growth and the use of mathematical modeling in preclinical anti-cancer drug investigations, but also may assist in defining how mathematical models could serve as potential prognostic tools in the clinic.

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Geographical breakdown

Country Count As %
Germany 1 <1%
Indonesia 1 <1%
Brazil 1 <1%
United Kingdom 1 <1%
Spain 1 <1%
Venezuela, Bolivarian Republic of 1 <1%
United States 1 <1%
Unknown 371 98%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 89 24%
Researcher 67 18%
Student > Bachelor 46 12%
Student > Master 37 10%
Student > Doctoral Student 16 4%
Other 51 13%
Unknown 72 19%
Readers by discipline Count As %
Engineering 58 15%
Agricultural and Biological Sciences 47 12%
Mathematics 41 11%
Medicine and Dentistry 34 9%
Biochemistry, Genetics and Molecular Biology 27 7%
Other 83 22%
Unknown 88 23%