Published Online: 17 Nov 2023 Page range: 178 - 184
Abstract
Abstract
Introduction: The geometrical precision of the machines is essential for effective and safe radiotherapy. Methods currently used for the measurement of the mechanical isocenter have many limitations. In this work, the optical system NaviRation for very precise measurement of mechanical accelerator isocenter is described. The results of the measurement of the isocenter for linear accelerator are also presented.
Materials and methods: An optical system for measuring the accelerator isocenter was designed and built. The optical system consists of two cameras recording the target position made according to a patented Zeiss technology. About 1,200 pairs of images are recorded during the rotation of the gantry, collimator and treatment table. Mathematical analysis of these images makes it possible to determine the location of the target center during rotation. In order to verify the accuracy of the measurements, a device simulating rotational motion was designed. The measurement results were also verified at the Central Office of Measures. The system must be calibrated each time before taking measurements. In this article, we present the results of measurements for the Versa HD accelerator.
Results: The accuracy of determining the current position of the axis of rotation was 0.15 mm. The time of taking measurements of all rotations does not exceed 20 minutes. Measurement results for the Versa HD accelerator showed that this accelerator met the criteria described by TG142 of the AAPM. The diameter of the gantry, collimator and table isocenter spheres were 1.5 mm, 0.3 mm and 0.4 mm, respectively.
Conclusions: The system enables precise, fast and simple mechanical isocenter measurement of the gantry, collimator and treatment table. It is also possible to perform all tests related to the measurements of distances, e.g. quality control of distance indicator, and distance of the table movement. The isocenter is measured independently of the accelerator for which measurements are made.
Published Online: 17 Nov 2023 Page range: 185 - 194
Abstract
Abstract
Introduction: To evaluate the clinical suitability of the current facility-based treatment plan protocol in establishing acceptability criteria.
Material and methods: Automated Volumetric Arc Therapy (VMAT) treatment plans were retrospectively evaluated for intact breast and chest-wall cancer patients from January 2021 to January 2023.
Results: A total of 94 patients were planned and treated using automated contouring and VMAT planning technique. The number of patients planned and treated for intact breast and chest-wall were 41 (43.6%) and 53 (56.4%), respectively. The mean intact breast volumes for optimization (Brst_opt) receiving 95% and 105% of the prescribed doses were 92.80% ± 1.11 and 1.54% ± 1.02, respectively. Their corresponding mean chest-wall volumes for optimization (Chst_opt) were 90.65% ± 3.19 and 2.28% ± 2.99, respectively. For left-sided cases, the mean heart dose received was 4.61 Gy ± 1.76 and 5.18 Gy ± 1.55 for intact breast plans and that for chest-wall plans, respectively. The mean ipsilateral lung volume receiving 20 Gy of the prescribed dose was 12.22% ± 3.86 and 13.19% ± 3.74 for intact breast plans and chest-wall plans, respectively. For the Brst_opt and Chst_opt dose metrics were calculated; the mean homogeneity index (HI) was 0.14 ± 0.03 and 0.15 ± 0.04, mean uniformity index (UI) was 1.09 ± 0.03 and 1.11 ± 0.03, and mean conformity index (CI) were 0.92 ± 0.04 and 0.91 ± 0.04, respectively.
Conclusions: The dosimetric evaluation shows a good dose distribution in the target volumes with minimal doses to the organs at risk (OAR). Assessment of the current data affirms the clinical usefulness of the facility-adopted protocol in achieving quality treatment plans for intact breast and chest-wall irradiations. The establishment of plan acceptability criteria will help achieve improved overall treatment outcomes.
Introduction: The geometrical precision of the machines is essential for effective and safe radiotherapy. Methods currently used for the measurement of the mechanical isocenter have many limitations. In this work, the optical system NaviRation for very precise measurement of mechanical accelerator isocenter is described. The results of the measurement of the isocenter for linear accelerator are also presented.
Materials and methods: An optical system for measuring the accelerator isocenter was designed and built. The optical system consists of two cameras recording the target position made according to a patented Zeiss technology. About 1,200 pairs of images are recorded during the rotation of the gantry, collimator and treatment table. Mathematical analysis of these images makes it possible to determine the location of the target center during rotation. In order to verify the accuracy of the measurements, a device simulating rotational motion was designed. The measurement results were also verified at the Central Office of Measures. The system must be calibrated each time before taking measurements. In this article, we present the results of measurements for the Versa HD accelerator.
Results: The accuracy of determining the current position of the axis of rotation was 0.15 mm. The time of taking measurements of all rotations does not exceed 20 minutes. Measurement results for the Versa HD accelerator showed that this accelerator met the criteria described by TG142 of the AAPM. The diameter of the gantry, collimator and table isocenter spheres were 1.5 mm, 0.3 mm and 0.4 mm, respectively.
Conclusions: The system enables precise, fast and simple mechanical isocenter measurement of the gantry, collimator and treatment table. It is also possible to perform all tests related to the measurements of distances, e.g. quality control of distance indicator, and distance of the table movement. The isocenter is measured independently of the accelerator for which measurements are made.
Introduction: To evaluate the clinical suitability of the current facility-based treatment plan protocol in establishing acceptability criteria.
Material and methods: Automated Volumetric Arc Therapy (VMAT) treatment plans were retrospectively evaluated for intact breast and chest-wall cancer patients from January 2021 to January 2023.
Results: A total of 94 patients were planned and treated using automated contouring and VMAT planning technique. The number of patients planned and treated for intact breast and chest-wall were 41 (43.6%) and 53 (56.4%), respectively. The mean intact breast volumes for optimization (Brst_opt) receiving 95% and 105% of the prescribed doses were 92.80% ± 1.11 and 1.54% ± 1.02, respectively. Their corresponding mean chest-wall volumes for optimization (Chst_opt) were 90.65% ± 3.19 and 2.28% ± 2.99, respectively. For left-sided cases, the mean heart dose received was 4.61 Gy ± 1.76 and 5.18 Gy ± 1.55 for intact breast plans and that for chest-wall plans, respectively. The mean ipsilateral lung volume receiving 20 Gy of the prescribed dose was 12.22% ± 3.86 and 13.19% ± 3.74 for intact breast plans and chest-wall plans, respectively. For the Brst_opt and Chst_opt dose metrics were calculated; the mean homogeneity index (HI) was 0.14 ± 0.03 and 0.15 ± 0.04, mean uniformity index (UI) was 1.09 ± 0.03 and 1.11 ± 0.03, and mean conformity index (CI) were 0.92 ± 0.04 and 0.91 ± 0.04, respectively.
Conclusions: The dosimetric evaluation shows a good dose distribution in the target volumes with minimal doses to the organs at risk (OAR). Assessment of the current data affirms the clinical usefulness of the facility-adopted protocol in achieving quality treatment plans for intact breast and chest-wall irradiations. The establishment of plan acceptability criteria will help achieve improved overall treatment outcomes.