CONVERSION OF DOSE DISTRIBUTION TO CELL SURVIVAL FRACTION THROUGH DNA DAMAGE: A MONTE CARLO STUDY
Ionizing radiation plays an important role in cancer treatment. Radiation is able to damage the genetic material of cells, blocking their ability to divide and proliferate further. Since radiation affects both healthy and malignant tissues, for all radiation treatments, the design of an accurate tre...
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Veröffentlicht in: | Radiation protection dosimetry 2022-10, Vol.198 (19), p.1462-1470 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Ionizing radiation plays an important role in cancer treatment. Radiation is able to damage the genetic material of cells, blocking their ability to divide and proliferate further. Since radiation affects both healthy and malignant tissues, for all radiation treatments, the design of an accurate treatment plan is fundamental. Usually, weight factors, such as the relative biological effectiveness, are applied to estimate the impact of the kind of radiation and the irradiated medium on the dose deposition. However, these factors can only provide a partial estimation of the real effect on tissues. In this work, a flexible system that is able to predict cell survival fractions according to the planned dose distribution is presented. Dose deposition and subsequent DNA damage were simulated with a multi-scale modeling approach by first applying the FLUKA Monte Carlo (MC) code to estimate the absorbed doses and fluence energy spectra and then using the MC Damage Simulation code to compute the DNA damage yields. Lastly, the results are converted into cell survival fraction using a theoretical model. The comparisons between the simulated survival fractions with experimental data are reported for a proton spread out Bragg peak at several doses. The presented approach helps to elucidate radiobiological responses along the Bragg curve and has the flexibility to be extended to a wide range of situations of clinical interest. |
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ISSN: | 0144-8420 1742-3406 |
DOI: | 10.1093/rpd/ncac191 |