Although VMAT delivery features continuous gantry rotation and leaf motion, dose calculation is often performed under the dual assumption of discrete apertures changing instantaneously from one discrete angle to the next. In this work, the validity of these two approximations is determined, as well as their impact on the quality of optimized plans. Further, an accurate method of fluence calculation is derived which does not use the discrete aperture approximation, but instead calculates the fluence as the multi-leaf collimator leaves sweep from one position to another. This continuous aperture fluence calculation is integrated in the VMAT optimization process using the open-source treatment planning system matRad. The three-step approach of VMAT optimization is used: fluence map optimization followed by leaf sequencing and direct aperture optimization, with variable leaf speed, gantry rotation speed, and MU rate. The benefit of the continuous aperture VMAT method over the discrete aperture method is determined by comparing the plan quality of discrete aperture and continuous aperture optimized plans, when the former is recalculated using the continuous aperture fluence calculation. Discrete aperture VMAT plans calculated at 4° spacing result in significant dose errors (10%–35%, depending on the anatomical site) as compared to the reference dose (continuous aperture fluence calculation at 0.5° spacing). These errors are greatly reduced (to 0.8%–2%) when the continuous aperture fluence calculation method was used at the same 4° spacing, implying that the dose error is primarily due to the discrete aperture approximation. Whereas all dose objectives were met by the discrete aperture VMAT optimized plan, many of them failed when the dose was recalculated with the continuous aperture fluence calculation. All objectives were met once again when the plan was optimized with the new continuous aperture VMAT optimization. Further, using only half of the beam angles, the continuous aperture VMAT optimization can achieve the same degree of accuracy with only 40% of the computing time as compared with the standard discrete aperture VMAT.
Purpose: The purpose of this work is to investigate the utility of plan class specific reference (PCSR) fields for predicting dosimeter response within isocentric and non‐isocentric composite clinical fields using the smallest fields employed by the CyberKnife radiosurgery system. Methods: Monte Carlo dosimeter response correction factors (CFs) were calculated for a plastic scintillator and microchamber dosimeter in 21 clinical fields and 9 candidate plan‐class PCSR fields which employ the 5, 7.5 and 10 mm diameter collimators. Measurements were performed in 5 PCSR fields to confirm the predicted relative response of detectors in the same field. Results: Ratios of corrected measured dose in the PCSR fields agree to within 1% of unity. Calculated CFs for isocentric fields agree within 1.5% of those for PCSR fields. Large and variable microchamber CFs are required for non‐isocentric fields, with differences as high as 5% between different clinical fields in the same plan class and 4% within the same field depending on the point of measurement. Non‐isocentric PCSR fields constructed to have relatively homogenous dose over a region larger than the detector have very different ion chamber CFs from clinical fields. The plastic scintillator detector has much more consistent response within each plan class but still require 3–4% corrections in some fields. Conclusions: While the PCSR field concept is useful for small isocentric fields, this approach may not be appropriate for non‐isocentric clinical fields which exhibit large and variable ion chamber CFs which differ significantly from CFs for homogenous field PCSRs.
Purpose To develop a framework for robust optimization of real‐time respiratory motion adaptive VMAT treatment plans, and to evaluate the robustness of resulting plans to variations in tumor trajectory during delivery. Methods The proposed framework is called aperture library‐enabled real‐time robust adaptation (ALERT‐RA). A patient‐specific library of optimized MLC apertures is defined for each combination of gantry angle and respiratory phase. The method assumes that the tumor is tracked in real‐time throughout delivery, and the aperture corresponding to the current phase and gantry angle will be delivered. The aperture library is optimized by considering all possible tumor trajectories determined by a probabilistic respiratory motion model. Plan robustness to trajectory variations was evaluated by sampling a trajectory, and determining the corresponding dose, from the respiratory model for each fraction. The cumulative dose of the full treatment course was simulated 50 times. Percentile dose–volume histograms (PDVHs) were computed from these simulated treatments. The resulting plan quality and robustness of this method were compared to other previously published motion 4D‐VMAT methods, including: an optimized tracking approach that assumes reproducible tumor motion, conformal tracking with aperture deformation, and a motion‐encompassing method. Two fractionation schemes were tested to determine the possible effect on robustness: a conventional fractionation of 66 Gy in 33 fractions, and an SBRT course with 60 Gy in 5 fractions. Results When considering target coverage, the ALERT‐RA method was found to produce a plan which was more robust than those produced using the optimized or conformal tracking methods. Using the PDVH analysis, the 5th and 95th percentiles of the prescription dose volume for the conventionally fractioned plan were found to be (respectively) 79% and 82% for the optimized tracking approach, 81% and 83% for the conformal tracking approach, and 92% and 97% using the new ALERT‐RA method. The motion‐encompassing plan was slightly more robust than the ALERT‐RA plan, with 5th and 95th percentiles at 94% and 95%, respectively. This came at a cost of higher dose to OARs, with the volume of lung receiving 5 Gy or more equal to 48% for the motion‐encompassing plan versus 44% for the ALERT‐RA plan. For the SBRT plan, the conformal tracking plan was similarly not robust, with 5th and 95th percentiles of the prescription dose volume equal to 88% and 89%. The optimized tracking SBRT plan gave values of 93% and 95%, and the motion‐encompassing plan 94% and 95%, while the ALERT‐RA gave values of 93% and 96%. The volume of lung receiving 20 Gy or more was slightly higher for the optimized tracking and motion‐encompassing plans compared to the ALERT‐RA plan, at 15%, 15%, and 14%, respectively. Conclusions Compared to other motion‐adaptive VMAT approaches, the ALERT‐RA algorithm is capable of delivering high‐quality plans which are robust to variations in tumor motion trajectories.
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