Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/21590
Title: Theoretical versus Ex Vivo Assessment of Radiation Damage Repair: An Investigation in Normal Breast Tissue
Authors: Ebert, Martin A.
Dhal, Bipina
Prunster, Janelle
McLaren, Sally
Zeps, Nikolajs
House, Michael
RENIERS, Brigitte 
Verhaegen, Frank
Corica, Tammy
Saunders, Christobel
Joseph, David J.
Issue Date: 2016
Publisher: RADIATION RESEARCH SOC
Source: RADIATION RESEARCH, 185 (4), p. 393-401
Abstract: In vivo validation of models of DNA damage repair will enable their use for optimizing clinical radiotherapy. In this study, a theoretical assessment was made of DNA double-strand break (DSB) induction in normal breast tissue after intraoperative radiation therapy (IORT), which is now an accepted form of adjuvant radiotherapy for selected patients with early breast cancer. DSB rates and relative biological effectiveness (RBE) were calculated as a function of dose, radiation quality and dose rate, each varying based on the applicator size used during IORT. The spectra of primary electrons in breast tissue adjacent to each applicator were calculated using measured X-ray spectra and Monte Carlo methods, and were used to inform a Monte Carlo damage simulation code. In the absence of repair, asymptotic RBE values (relative to Co-60) were approximately 1.5. Beam-quality changes led to only minor variations in RBE among applicators, though differences in dose rate and overall dose delivery time led to larger variations and a rapid decrease in RBE. An experimental assessment of DSB induction was performed ex vivo using pre- and postirradiation tissue samples from patients receiving breast intraoperative radiation therapy. Relative DSB rates were assessed via c-H2AX immunohistochemistry using proportional staining. Maximum-likelihood parameter estimation yielded a DSB repair halftime of 25.9 min (95% CI, 21.5-30.4 min), although the resulting model was not statistically distinguishable fromone where there was no change in DSB yield among patients. Although the model yielded an in vivo repair halftime of the order of previous estimates for in vitro repair halftimes, we cannot conclude that it is valid in this context. This study highlights some of the uncertainties inherent in population analysis of ex vivo samples, and of the quantitative limitations of immunohistochemistry for assessment of DSB repair. (C) 2016 by Radiation Research Society
Notes: [Ebert, Martin A.; Prunster, Janelle; Corica, Tammy; Joseph, David J.] Sir Charles Gairdner Hosp, Dept Radiat Oncol, Nedlands, WA 6009, Australia. [Ebert, Martin A.; Dhal, Bipina; House, Michael] Univ Western Australia, Sch Phys, Crawley, WA, Australia. [Zeps, Nikolajs; Saunders, Christobel; Joseph, David J.] Univ Western Australia, Sch Surg, Crawley, WA, Australia. [Corica, Tammy] Univ Western Australia, Sch Med & Pharmacol, Crawley, WA, Australia. [McLaren, Sally; Zeps, Nikolajs] St John God Subiaco Hosp, Perth, WA, Australia. [Reniers, Brigitte] Hasselt Univ, CMK, Res Grp NuTeC, Diepenbeek, Belgium. [Verhaegen, Frank] Maastro Clin, Maastricht, Netherlands.
Document URI: http://hdl.handle.net/1942/21590
ISSN: 0033-7587
e-ISSN: 1938-5404
DOI: 10.1667/RR14235.1
ISI #: 000376752200007
Rights: © 2016 by Radiation Research Society. All rights of reproduction in any form reserved.
Category: A1
Type: Journal Contribution
Validations: ecoom 2017
Appears in Collections:Research publications

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