4.6 Article

Spatial Metrics of Tumour Vascular Organisation Predict Radiation Efficacy in a Computational Model

Journal

PLOS COMPUTATIONAL BIOLOGY
Volume 12, Issue 1, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pcbi.1004712

Keywords

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Funding

  1. National Institutes of Health Loan Repayment Grant
  2. National Cancer Institute [U54 CA143970, U01 CA151924]
  3. EPSRC [EP/I017909/1] Funding Source: UKRI
  4. Engineering and Physical Sciences Research Council [EP/I017909/1] Funding Source: researchfish
  5. NATIONAL CANCER INSTITUTE [U54CA143970, U01CA151924] Funding Source: NIH RePORTER

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Intratumoural heterogeneity is known to contribute to poor therapeutic response. Variations in oxygen tension in particular have been correlated with changes in radiation response in vitro and at the clinical scale with overall survival. Heterogeneity at the microscopic scale in tumour blood vessel architecture has been described, and is one source of the underlying variations in oxygen tension. We seek to determine whether histologic scale measures of the erratic distribution of blood vessels within a tumour can be used to predict differing radiation response. Using a two-dimensional hybrid cellular automaton model of tumour growth, we evaluate the effect of vessel distribution on cell survival outcomes of simulated radiation therapy. Using the standard equations for the oxygen enhancement ratio for cell survival probability under differing oxygen tensions, we calculate average radiation effect over a range of different vessel densities and organisations. We go on to quantify the vessel distribution heterogeneity and measure spatial organization using Ripley's L function, a measure designed to detect deviations from complete spatial randomness. We find that under differing regimes of vessel density the correlation coefficient between the measure of spatial organization and radiation effect changes sign. This provides not only a useful way to understand the differences seen in radiation effect for tissues based on vessel architecture, but also an alternate explanation for the vessel normalization hypothesis.

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