Purpose: The dosimetric accuracy of the recently released Acuros XB advanced dose calculation algorithm (Varian Medical Systems, Palo Alto, CA) is investigated for single radiation fields incident on homogeneous and heterogeneous geometries, as well as for two arc (VMAT) cases and compared against the analytical anisotropic algorithm (AAA), the collapsed cone convolution superposition algorithm (CCCS) and Monte Carlo (MC) calculations for the same geometries. Methods and Materials: Small open fields ranging from 1 × 1 cm 2 to 5 × 5 cm 2 were used for part of this study. The fields were incident on phantoms containing lung, air, and bone inhomogeneities. The dosimetric accuracy of Acuros XB, AAA and CCCS in the presence of the inhomogeneities was compared against BEAMnrc/DOSXYZnrc calculations that were considered as the benchmark. Furthermore, two clinical cases of arc deliveries were used to test the accuracy of the dose calculation algorithms against MC. Results: Open field tests in a homogeneous phantom showed good agreement between all dose calculation algorithms and MC. The dose agreement was +/−1.5% for all field sizes and energies. Dose calculation in heterogenous phantoms showed that the agreement between Acuros XB and CCCS was within 2% in the case of lung and bone. AAA calculations showed deviation of approximately 5%. In the case of the air heterogeneity, the differences were larger for all calculations algorithms. The calculation in the patient CT for a lung and bone (paraspinal targets) showed that all dose calculation algorithms predicted the dose in the middle of the target accurately; however, small differences (2%-5%) were observed at the low dose region. Overall, when compared to MC, the Acuros XB and CCCS had better agreement than AAA. Conclusions: The Acuros XB calculation algorithm in the newest version of the Eclipse treatment planning system is an improvement over the existing AAA algorithm. The results are comparable to CCCS and MC calculations especially for both stylized and clinical cases. Dose discrepancies were observed for extreme cases in the presence of air inhomogeneities.
Specialized techniques that make use of small field dosimetry are common practice in today's clinics. These new techniques represent a big challenge to the treatment planning systems due to the lack of lateral electronic equilibrium. Because of this, the necessity of planning systems to overcome such difficulties and provide an accurate representation of the true value is of significant importance. Pinnacle3 is one such planning system. During the IMRT optimization process, Pinnacle3 treatment planning system allows the user to specify a minimum segment size which results in multiple beams composed of several subsets of different widths. In this study, the accuracy of the engine dose calculation, collapsed cone convolution superposition algorithm (CCCS) used by Pinnacle3, was quantified by Monte Carlo simulations, ionization chamber, and Kodak extended dose range film (EDR2) measurements for 11 SBRT lung patients. Lesions were < 3.0 cm in maximal diameter and <27.0 cm3 in volume. The Monte Carlo EGSnrc\BEAMnrc and EGS4\MCSIM were used in the comparison. The minimum segment size allowable during optimization had a direct impact on the number of monitor units calculated for each beam. Plans with the smallest minimum segment size (0.1 cm2 to 2.0 cm2) had the largest number of MUs. Although PTV coverage remained unaffected, the segment size did have an effect on the dose to the organs at risk. Pinnacle3‐calculated PTV mean doses were in agreement with Monte Carlo‐calculated mean doses to within 5.6% for all plans. On average, the mean dose difference between Monte Carlo and Pinnacle3 for all 88 plans was 1.38%. The largest discrepancy in maximum dose was 5.8%, and was noted for one of the plans using a minimum segment size of 0.1 cm2. For minimum dose to the PTV, a maximum discrepancy between Monte Carlo and Pinnacle3 was noted of 12.5% for a plan using a 6.0 cm2 minimum segment size. Agreement between point dose measurements and Pinnacle3‐calculated doses were on average within 0.7% in both phantoms. The profiles show a good agreement between Pinnacle3, Monte Carlo, and EDR2 film. The gamma index and the isodose lines support the result.PACS number: 87.56.bd
The purpose of this study is to evaluate 3D dose reconstruction of pretreatment verification plans using multiple 2D planes acquired from the OCTAVIUS phantom and the Seven29 detector array. Eight VMAT patient treatment plans of different sites were delivered onto the OCTAVIUS phantom. The plans span a variety of tumor site locations from low to high plan complexity. A patient specific quality assurance (QA) plan was created and delivered for each of the 8 patients using the OCTAVIUS phantom in which the Seven29 detector array was placed. Each plan was delivered four times by rotating the phantom in 45° increments along its longitudinal axis. The treatment plans were delivered using a Novalis Tx with the HD120 MLC. Each of the four corresponding planar doses was exported as a text file for further analysis. An in-house MATLAB code was used to process the planar dose information. A cylindrical geometry-based, linear interpolation method was utilized to generate the measured 3D dose reconstruction. The TPS calculated volumetric dose was exported and compared against the measured reconstructed volumetric dose. Dose difference, dose area histograms (DAH), isodose lines, profiles, 2D and 3D gamma were used for evaluation. The interpolation method shows good agreement (<2%) between the planned dose distributions in the high dose region but shows discrepancies in the low dose region. Horizontal profiles, dose area histograms and isodose lines show good agreement for the sagittal and coronal planes but demonstrate slight discrepancies in the transverse plane. The 3D gamma index average was 92.4% for all patients when a 5%/5 mm gamma passing rate criteria was employed but dropped to <80.1% on average when parameters were reduced to 2%/2 mm. A simple cylindrical geometry-based, linear interpolation method is able to predict good agreement in the high dose region between the reconstructed volumetric dose and the planned volumetric dose. It is important to mention that the interpolation algorithm introduces dose discrepancies in small regions within the high dose gradients due to the interpolation itself. However, the work presented serves as a good starting point to establish a benchmark for the level of manipulation necessary to obtain 3D dose delivery quality assurance using current technology.
Purpose: The aim of the study is to evaluate and compare the four different commercial devices for Rapid Arc and Sliding Window IMRT QA. Materials and methods: Fifteen consecutive RapidArc plans and ten IMRT plans were used for this study. All plans were optimized using Eclipse TPS. For all plans, the corresponding verification dose distributions were calculated using four (n=4) geometries. This include an acrylic phantom with film, the IBA with the MatrixX, the PTW Octavious phantom with the seven29 array, and the Scandidos Delta4 device. All plans and deliveries were calculated and delivered using the actual planned gantry and collimator angles respectively. All measurements were compared against the calculated ones, first by taking into account all points in the measurement planes and second by applying a threshold value where the points that received less than 20% of the normalized dose were excluded from the gamma index calculation. Results:Among these 25 plans, using all available points for the gamma calculation, all of them passed the criteria (3.0% and 3mm DTA) of having gamma values ≤ 1 (more than 90% of points). A few verification plans failed to pass the set gamma criteria when the evaluated points were limited to those only receiving more than 20% of the maximum dose. On average all the QA devices produced very similar results. This was further supported by the Bland‐Altman analysis that was performed and showed that all the calculated gamma values of all detectors were within 5% from those of film. Conclusions: The results showed that there insignificant differences between the detectors. All patient QAs passed the routine clinically criteria of gamma index values of 3% dose difference and 3mm DTA. We conclude that the dosimetric systems under investigation can be used interchangeably for routine patient specific QA. “Research sponsored by PTW‐Freiburg Company.”
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