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Time resolved dose rate distributions in brachytherapy.

作者信息

Peppa Vasiliki, Pappas Eleftherios P, Karaiskos Pantelis, Papagiannis Panagiotis

机构信息

Medical Physics Laboratory, Medical School, National and Kapodistrian University of Athens, Athens, Greece.

Medical Physics Laboratory, Medical School, National and Kapodistrian University of Athens, Athens, Greece.

出版信息

Phys Med. 2017 Sep;41:13-19. doi: 10.1016/j.ejmp.2017.04.013. Epub 2017 Apr 28.

DOI:10.1016/j.ejmp.2017.04.013
PMID:28457787
Abstract

PURPOSE

To investigate the biological significance of introducing time-resolved dose rate distributions (TR-DRD) in brachytherapy.

MATERIALS AND METHODS

The treatment plan of a head and neck patient treated with pulsed-dose-rate (PDR) brachytherapy was considered. The TR-DRD was calculated on the basis of a Monte Carlo generated single source dose rate matrix taking into account the dose rate per source dwell position. Biologically Effective Dose (BED) was obtained considering either the mean dose rate per pulse (analytical method) or the TR-DRD (numerical method). Corresponding Tumor Control Probabilities (TCP) were calculated and compared for various PDR schemes and repair half-times from the literature. The dose of the biologically equivalent high-dose-rate (HDR) treatment schedule was also evaluated.

RESULTS

The analytical method presents an overall BED underestimation (up to 2%) relative to TR-DRD results. This is associated with an analytical-based TCP underestimation which increases with dose/pulse, pulse duration and period time and decreases with total dose. The half-time of repair seems to have the largest impact on the TCP calculations, with significant differences (up to 39.1%) corresponding to the shorter repair half-times. Regarding the equivalent HDR treatment schedule, the analytical method resulted to a HDR isoeffective dose underestimation lower than 2.2% and thus does not warrant any change in the derivation of the equivalent HDR scheme.

CONCLUSION

TR-DRD data should be taken into account for PDR biological effectiveness estimations, especially for short tissue repair half-times. This does not appear however to influence dose prescription of the equivalent HDR treatment schedule for mobile tongue carcinoma.

摘要

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