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Abstract
Tumor growth is the result of the interplay of complex biological processes in huge numbers of individual cells living in changing environments. Effective simple mathematical laws have been shown to describe tumor growth in vitro, or simple animal models with bounded-growth dynamics accurately. However, results for the growth of human cancers in patients are scarce. Our study mined a large dataset of 1133 brain metastases (BMs) with longitudinal imaging follow-up to find growth laws for untreated BMs and recurrent treated BMs. Untreated BMs showed high growth exponents, most likely related to the underlying evolutionary dynamics, with experimental tumors in mice resembling accurately the disease. Recurrent BMs growth exponents were smaller, most probably due to a reduction in tumor heterogeneity after treatment, which may limit the tumor evolutionary capabilities. In silico simulations using a stochastic discrete mesoscopic model with basic evolutionary dynamics led to results in line with the observed data.
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1 University of Castilla-La Mancha, Ciudad Real, Spain (GRID:grid.8048.4) (ISNI:0000 0001 2194 2329)
2 Sanchinarro University Hospital, HM Hospitales, Madrid, Spain (GRID:grid.428486.4) (ISNI:0000 0004 5894 9315)
3 Hospital Regional Universitario de Málaga, Málaga, Spain (GRID:grid.411457.2)
4 MD Anderson Cancer Center, Madrid, Spain (GRID:grid.428844.6) (ISNI:0000 0004 0455 7543)
5 Salamanca University Hospital, Salamanca, Spain (GRID:grid.11762.33) (ISNI:0000 0001 2180 1817)
6 Spanish National Cancer Research Centre (CNIO), Brain Metastasis Group, Madrid, Spain (GRID:grid.7719.8) (ISNI:0000 0000 8700 1153)
7 Hospital Universitario La Paz, Madrid, Spain (GRID:grid.81821.32) (ISNI:0000 0000 8970 9163)
8 Fundación Instituto Valenciano de Oncología, Valencia, Spain (GRID:grid.418082.7) (ISNI:0000 0004 1771 144X)