ESTRO 2024 - Abstract Book
S4948
Physics - Quality assurance and auditing
ESTRO 2024
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[4] Hossain M. Output trends, characteristics, and measurements of three megavoltage radiotherapy linear accelerators. J Appl Clin Med Phys. 2014; 15(4): 137-151. https://doi.org/10.1120/jacmp.v15i4.4783
[5] Matsumoto K, Tarutani K. Characteristics of Monitor Chamber for Photon Energy Mounted on Linear Accelerators. Nihon Hoshasen Gijutsu Gakkai Zasshi. 2019 ;75(10):1135-1140. https://doi.org/10.6009/jjrt.2019_jsrt_75.10.1135
3215
Digital Poster
Biological basis for dosimetric audit criteria for Head&Neck radiotherapy
Vanessa Panettieri 1,2,3 , Paige Taylor 4,5 , Stephen F Kry 4,5
1 Peter MacCallum Cancer Centre, Physical Sciences, Melbourne, Australia. 2 The University of Melbourne, Sir Peter MacCallum Department of Oncology, Melbourne, Australia. 3 Monash University, Central Clinical School, Melbourne, Australia. 4 Imaging and Radiation Oncology Core, ,, Houston, USA. 5 MD Anderson Cancer Center, Department of Radiation Physics, Houston, USA
Purpose/Objective:
Current clinical trial credentialing criteria solely relies on physical quantities (such as dose and dose distribution), which act as surrogate of the biological response [1]. In North American trials involving IMRT, credentialing is required based on irradiation of a phantom based on H&N anatomy provided by the Imaging and Radiation Oncology Core (IROC). In order to be successful, measured and planned dose must agree within 7% at each of the 6 locations of point dose measurement. This “maximum point-dose disagreement” fails to account for the dose distribution, and is independent of the actual anatomical site of the trial. As such, this approach could potentially mask the true sensitivity to inaccurate dose delivery.
The aim of this work is to evaluate credentialing criteria guided directly by biological variations in the anatomy treated, using biological indices.
Material/Methods:
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