Accurate dosimetry is a fundamental requirement for the safe and efficient use of radiation in medical applications. International Codes of Practice, such as IAEA TRS-398 (2000) for radiotherapy beams and IAEA TRS-457 (2007) for diagnostic radiology beams, provide the necessary formulation for reference and relative dosimetry and the data required for their implementation. Research in recent years has highlighted the shortage of such data for radiotherapy small photon beams and for surface dose estimations in diagnostic and interventional radiology, leading to significant dosimetric errors that in some instances have jeopardized patient’s safety and treatment efficiency. The aim of this thesis is to investigate and determine key data for the reference and relative dosimetry of radiotherapy and radiodiagnostics beams. For that purpose the Monte Carlo system PENELOPE has been used to simulate the transport of radiation in different media and a number of experimental determinations have also been made. A review of the key data for radiotherapy beams published after the release of IAEA TRS-398 was conducted, and in some cases the considerable differences found were questioned under the criterion of data consistency throughout the dosimetry chain (from standards laboratories to the user). A modified concept of output factor, defined in a new international formalism for the dosimetry of small photon beams, requires corrections to dosimeter readings for the dose determination in small beams used clinically. In this work, output correction factors were determined, for Varian Clinac 6 MV photon beams and Leksell Gamma Knife Perfexion 60Co gamma-ray beams, for a large number of small field detectors, including air and liquid ionization chambers, shielded and unshielded silicon diodes and diamond detectors, all of which were simulated by Monte Carlo with great detail. Backscatter factors and ratios of mass energy-absorption coefficients required for surface (skin) determinations in diagnostic and interventional radiology applications were also determined, as well as their extension to account for non-standard phantom thicknesses and materials. A database of these quantities was created for a broad range of monoenergetic photon beams and computer codes developed to convolve the data with clinical spectra, thus enabling the determination of key data for arbitrary beam qualities. Data presented in this thesis has been contributed to the IAEA international dosimetry recommendations for small radiotherapy beams and for diagnostic radiology in paediatric patients. / <p>At the time of the doctoral defense, the following paper was unpublished and had a status as follows: Paper 6: Manuscript.</p>

Radiotherapy is used in clinics to treat cancer with highly energetic ionizing particles. The radiation dose can be measured indirectly by means of radiation detectors or dosimeters. The dose deposited in a detector can be related to dose deposited in a point within the patient. In theory, however, this is only possible under charged particle equilibrium (CPE). The motivation behind the dissertation was driven by the difficult, yet crucial, dosimetry in non-CPE regions. Inaccurate dose assessment performed with standard dosimetry using ionization chambers may significantly impact the outcomes of radiotherapy treatments. Therefore, advanced dosimetry methods tailored specifically to suit non-CPE conditions must be used. This work aims to improve dosimetry in two types of non-CPE conditions that pose dosimetric challenges: regions near interfaces of tissues with low- and high- density media and in small photon fields. To achieve the main dissertation objectives, an enhanced film dosimetry protocol with a novel film calibration approach was implemented. This calibration method is based on the percent depth dose (PDD) tables and was shown to be efficient and accurate. As a result, the PDD calibration method was used for the film dosimetry process throughout the dissertation work. Monte Carlo (MC) calculations for the small field dosimetry were performed using phase-space files (PSFs) provided by Varian for TrueBeam linac. The MC statistical uncertainty in these types of calculations is limited by the number of particles (due to latent variance) in the used PSFs. This study investigated the behaviour of the latent variances (LV) with beam energy, depth in phantom, and calculation resolution (voxel size). LV was evaluated for standard 10x10 cm2 fields as well as small fields (down to 1.3 mm diameter). The results showed that in order to achieve sub-percent LV in open 10x10 cm2 field MC simulations a single PSF can be used, whereas for small SRS fields (1.3—10 mm) more PSFs (66—8 PSFs) would have to be summed. The first study in this dissertation compared the performance of several dosimetric methods in three multi-layer heterogeneous phantoms with water/air, water/lung, and water/steel interfaces irradiated with 6 and 18 MV photon beams. MC calculations were used, along with Acuros XB, anisotropic analytical algorithm (AAA), GafChromic EBT2 film, and MOSkin dosimeters. PDDs were calculated and measured in these heterogeneous phantoms. The result of this study showed that Acuros XB, AAA, and MC calculations were within 1% in the regions with CPE. At media interfaces and buildup regions, differences between Acuros XB and MC were in the range of +4.4% to -12.8%. MOSkin and EBT2 measurements agreed to MC calculations within ~ 2.5%-4.5%. AAA did not predict the backscatter dose from the high-density heterogeneity. For the third, multilayer lung phantom, 6 MV beam PDDs calculated by all treatment planning system (TPS) algorithms were within 2% of MC. 18 MV PDDs calculated by Acuros XB and AAA differed from MC by up to 3.2 and 6.8%, respectively. MOSkin and EBT2 each differed from MC by up to 3%. All dosimetric techniques, except AAA, agreed within 3% in the regions with particle equilibrium. Differences between the dosimetric techniques were larger for the 18 MV than the 6 MV beam. This study provided a comparative performance evaluation of several advanced dosimeters in heterogeneous phantoms. This combination of experimental and calculation dosimetry techniques was used for the first time to evaluate the dose near these interfaces. The second study in the dissertation aims to improve dose measurement accuracy in small radiotherapy fields. Field output factors of 6 MV beams from TrueBeam linear accelerator (linac) collimated with 1.27-40 mm diameter cones were calculated and measured using MC and EBT3 films. A set of detector specific correction factors for two widely used dosimeters (EFD-3G diode and PTW-60019 microDiamond detectors) were determined based on GafChromic EBT3 film measurements and calculated using MC methods. MC calculations were performed for microDiamond detector in parallel and perpendicular orientations relative to the beam axis. The result of this study showed that the measured OFs agreed within 2.4% for fields ≥10 mm. For the cones of 1.27, 2.46, and 3.77 mm diameter maximum differences were 17.9%, 1.8% and 9.0%, respectively. MC calculated OF in water agreed with those obtained using EBT3 film within 2.2% for all fields. MC calculated output correction factors for microDiamond detector in fields ≥10 mm ranged within 0.975-1.020 for perpendicular and parallel orientations. MicroDiamond detector correction factors calculated for the 1.27, 2.46 and 3.77 mm fields were 1.974, 1.139 and 0.982 with detector in parallel orientation, and these factors were 1.150, 0.925 and 0.914 in perpendicular orientation. EBT3 and MC obtained correction factors agreed within 3.7% for fields of ≥3.77 mm and within 5.9% for smaller cones. This work provided output correction factors for microDiamond and EFD-3G detectors in very small fields of 1.27 – 3.77 mm diameter and demonstrated over and under-response of these detectors in such fields. These correction factors allow improve the accuracy of dose measurements in small photon fields using these detectors. / Graduate / 2019-08-30