OAR@½ñÈÕºÚÁÏ Community:/library/oar/handle/123456789/22812026-08-14T10:08:12Z2026-08-14T10:08:12ZExtended commissioning and validation of the comprehensive motion management (CMM) system on an Elekta Unity MR-Linac/library/oar/handle/123456789/1427182026-01-14T10:45:29Z2025-01-01T00:00:00ZTitle: Extended commissioning and validation of the comprehensive motion management (CMM) system on an Elekta Unity MR-Linac
Abstract: Background The Elekta Unity MR-Linac (MRL), operational at Sir Anthony Mamo
Oncology Centre (SAMOC) since July 2024, enables daily adaptive radiotherapy
(ART) by adjusting treatment plans to account for tumour and anatomical changes.
The Comprehensive Motion Management (CMM) system allows real-time motion
tracking and gated beam delivery using different strategies, prompting the need for
extended commissioning and validation to characterise performance under varied
clinical conditions.
Objectives To design and deliver extended commissioning and validation tests on
the Elekta CMM system, to quantify its positional and dosimetric accuracy across
three selected gating strategies (respiratory, exhale navigated, and non-respiratory),
and identify any potential limitations.
Research Methodology The MRI4D MODUS QUASARTM phantom was commissioned to verify its positional accuracy, forming the basis for subsequent tests. A number of motion traces were used to challenge the system for the three gating strategies. Selected traces were used to quantify the Anatomic Position Monitoring (APM) positional accuracy, measure beam gating latency for both beam-on/off
transitions, and assess the dosimetric impact of these parameters during different
strategies. The dosimetric impact of different gating thresholds, volumetric overlapping criterion (VOICE) percentages, and complex waveforms was characterised using EBT4 film dosimetry.
Results APM analysis confirmed reliable target localisation within typically <±1
mm across all strategies. In the respiratory strategy, regular waveforms met the
manufacturer’s latency specification, while irregular waveforms showed degraded
performance. Film measurements for respiratory strategy indicated that regular
breathing traces maintained target coverage (−0.40±0.22mm change in prescription
isodose), while irregular breathing may compromise dose conformity and reduce
clinical target volume (CTV) coverage (−1.22±0.23mm change). A trade-off was
evident between gating window and efficiency: tighter gating thresholds (2mm)
and VOICE 100% improved coverage (0.25±0.20 and 0.08±0.21mm) compared with
5mm and VOICE 95% (–1.13±0.29 and –1.53±0.21mm), but at the cost of delivery
efficiency (3.3-5.5× longer). All gating scenarios retained gamma pass rates >97%
(3%/2 mm), but a slight reduction was observed for challenging deliveries.
Conclusions and Recommendations The CMM system demonstrated robust performance under regular conditions but limitations where characterised under irregular motion including CTV coverage reduction and may need to be accounted for clinically but further investigation is required. Future work should validate CMM in lung-equivalent 4D phantoms and further assess the exhale-navigated strategy.
Description: M.Sc. Med.Phy.(Melit.)2025-01-01T00:00:00ZTLD-based organ dosimetry in abdomino-pelvic CT/library/oar/handle/123456789/1427162026-01-14T10:41:35Z2025-01-01T00:00:00ZTitle: TLD-based organ dosimetry in abdomino-pelvic CT
Abstract: Background Ideally, patient organ dosimetry should follow a direct in-vivo approach. However, owing to a lack of feasibility of such an approach, Monte-Carlo
(MC) simulations are the gold standard for estimating organ absorbed doses. Such
simulation software must be verified via measurements using physical dosimeters
calibrated at the beam energy. However, calibration methods of such dosimeters
often use high-energy sources without inclusion of lower-energy scattered photons,
which reduces calibration accuracy. A direct calibration using Computed Tomography (CT) spectra is desired.
Objectives This research investigated how organ doses within the abdomino-pelvic region are affected by CT beam energy. A calibration method was proposed to include the impact of scatter.
Research Methodology Thermoluminescent Dosimeter (TLD) dose measurements were made in 9 separate organs within an adult male anthropomorphic phan tom on an abdomino-pelvis protocol. Readings were taken at two different beam
energies (120kVp, 140kVp). For each energy, the crystals were read using 2 different
calibration profiles, one developed on a planar radiography system (without scatter) and using a 3D-printed insert and CT Dose Index (CTDI) phantom directly on
the CT scanner (with scatter).
Results An increase of 11.3% mGy normalized mean was observed in organ
doses between the two energy levels. There was a significant proportional bias
between results from the two calibration methods.
Conclusions and Recommendations To our knowledge, this is the first study
to consider calibrating TLD crystals directly at a CT scanner.
Description: M.Sc. Med.Phy.(Melit.)2025-01-01T00:00:00ZValidation of a motion management and gating protocol on the Elekta Unity MR LINAC for margin reduction in prostate cancer/library/oar/handle/123456789/1427152026-01-14T10:40:06Z2025-01-01T00:00:00ZTitle: Validation of a motion management and gating protocol on the Elekta Unity MR LINAC for margin reduction in prostate cancer
Abstract: Background: The recent installation of Elekta Unity MR-LINAC (MRL) at the
Sir Anthony Mamo Oncology Centre (SAMOC) integrates magnetic resonance imaging (MRI) with radiotherapy delivery. The system offers superior soft tissue visualisation and motion management capabilities, particularly relevant for prostate cancer, where intrafractional motion compromises dose coverage and increased exposure to organs at risk (OAR).
Objectives: This study aimed to evaluate the feasibility, performance, and limitations of a reduced margin protocol for prostate radiotherapy on the Elekta Unity
MRL. Therefore, the validation of treatment margin reduction was essential to ensure safe margin reduction and effective treatment delivery in a typical clinical setting for prostate treatments.
Research Methodology: The analysis of 360 treatment fractions was performed
to characterise prostate motion using Unity log files. Then, a treatment planning
study with a phantom was performed to simulate prostate displacements and evaluate dose–volume histogram (DVH) metrics using Monaco® TPS. Lastly, radiochromic
film dosimetry validated treatment delivery under static and motion scenarios,
with gamma analysis used for dose comparison.
Results: The log file analysis showed minimal motion in the LR and AP directions, but higher variability in the SI axis, especially during the final 30 seconds
of treatment. DVH analysis revealed that most treatment plans met dosimetric
criteria, though extremely inferior displacements reduced target coverage. Film
dosimetry and gamma analysis showed that the film exposed during motion with
2 baselineshifts (BLS) and the film exposed at 97% VOICE performed the best and
poorest, respectively.
Conclusions and Recommendations: This study shows that reducing prostate
PTV margins to 2 mm is possible. Moreover, it was concluded that BLS can restore
margin coverage. Clinically, combining margin optimisation with adaptive work-flows and quality assurance QA practices enhances safety and precision. Future
research should validate results in larger cohorts, consider seminal vesicle motion,
and apply such strategies across other anatomically mobile sites.
Description: M.Sc. Med.Phy.(Melit.)2025-01-01T00:00:00ZEnvironmental dose evaluation following the installation of a SPECT/CT scanner in a major public hospital using Monte Carlo simulation/library/oar/handle/123456789/1427132026-01-14T10:31:21Z2025-01-01T00:00:00ZTitle: Environmental dose evaluation following the installation of a SPECT/CT scanner in a major public hospital using Monte Carlo simulation
Abstract: Background: Accurate shielding design in nuclear medicine requires reliable dose estimates to maintain occupational and public exposures as low as reasonably achievable.
Shielding calculations are conventionally performed analytically. A Monte Carlo (MC) approach offers more detailed, site-specific insight but has not yet been systematically applied locally.
Objectives: Acquire proficiency in FLUKA; develop a detailed model of a site-specific
SPECT/CT facility; simulate a typical 99mTc imaging protocol; benchmark the model against
experimental data and national dose regulations; extend the framework to 177Lu.
Research Methodology: A hybrid approach combining simulation, experimental measurements, and analytical calculations was adopted. The facility and scanner were modelled based on technical drawings and material data. Ambient dose equivalents were physically measured at multiple locations using thermoluminescent dosimeters exposed to a 99mTc-injected phantom for model validation. Quantities scored in FLUKA included ambient dose equivalents, fluence distributions, regional energy deposition, and fluence-energy spectra.
Dose equivalents were normalised to clinical workloads to derive annual dose estimates.
Results: A high-fidelity MC model of the SPECT/CT facility was successfully developed,
simulated and validated. Weighted mean ratios and two-tailed paired t-tests (n = 11)
showed values of 1.17 ± 0.02 (analytical vs experiment, significant, p < 0.03) and 1.20 ± 0.01
(simulation vs experiment, not significant, p = 0.10). The ratio findings indicated that
the MC method performed at least as well as the analytical approach, while the paired t-test suggested superior performance. Workload-adjusted annual dose equivalents verified
compliance of installed shielding with national dose limits and regional energy deposition
revealed strong phantom self-absorption (62% for 99mTc, 87% for 177Lu).
Conclusions and Recommendations: This study introduced and validated an MC facility
model for nuclear medicine shielding assessment. Future planning should combine analytical, experimental, and MC methods for accurate, yet time-efficient assessments. Further work should address validation against alternative MC codes, CT source modelling, and dynamic patient and equipment motion.
Description: M.Sc. Med.Phy.(Melit.)2025-01-01T00:00:00Z