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ZAP-X 治疗计划系统和射束数据验证:一种新型自屏蔽立体定向放射外科系统。

Treatment planning system and beam data validation for the ZAP-X: A novel self-shielded stereotactic radiosurgery system.

机构信息

Department of Radiation Oncology, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, AZ, USA.

出版信息

Med Phys. 2021 May;48(5):2494-2510. doi: 10.1002/mp.14740. Epub 2021 Apr 1.

DOI:10.1002/mp.14740
PMID:33506520
Abstract

PURPOSE

To evaluate the treatment planning system (TPS) performance of the ZAP-X stereotactic radiosurgery (SRS) system through nondosimetric, dosimetric, and end-to-end (E2E) tests.

METHODS

A comprehensive set of TPS commissioning and validation tests was developed using published guidelines. Nondosimetric validation tests included information transfer, computed tomography-magnetic resonance (CT-MR) image registration, structure/contouring, geometry, dose tools, and CT density. Dosimetric validation included comparisons between TPS and water tank/Solid Water measurements for various geometries and beam arrangements and end-to-end (E2E) tests. Patient-specific quality assurance was performed with an ion chamber in the Lucy phantom and with Gafchromic EBT3 film in the CyberKnife head phantom. RadCalc was used for independent verification of monitor units. Additional E2E tests were performed using the RPC Gamma Knife thermoluminescent dosimeter (TLD) phantom, MD Anderson SRS head phantom, and PseudoPatient gel phantom for independent absolute dose verification.

RESULTS

CT-MR image registrations with known translational and rotational offsets were within tolerance (<0.5 × maximum voxel dimension). Slice thickness and distance accuracy were within 0.1 mm, and volume accuracy was within 0 to 0.11 cm . Treatment planning system volume measurement uncertainty was within 0.1 to 0.4 cm . Ion chamber point-dose measurements for a single beam in a water phantom agreed to TPS-calculated values within ±4% for collimator diameters 10 to 25 mm, and ±6% for 7.5 mm, for all measured depths (7, 50, 100, 150, and 200 mm). In homogeneous Solid Water, point-dose measurements agreed to within ±4% for cones sizes 7.5 to 25 mm. With 1-cm high/low density inserts, measurements were within ±4.2% for cone sizes 10 to 25 mm. Film-based E2E using 4/5-mm cones resulted in a gamma passing rate (%GP) of 99.8% (2%/1.5 mm). Point-dose measurements in a Lucy phantom with an ion chamber using 36 beams distributed along three noncoplanar arcs agreed to within ±4% for cone sizes 10 to 25 mm. The RPC Gamma Knife TLD phantom yielded passing results with a measured-to-expected TLD dose ratio of 1.02. The MD Anderson SRS head phantom yielded passing results, with 4% TLD agreement and %GP of 95%/93% (5%/3 mm) for coronal/sagittal film planes. The RTsafe gel phantom gave %GP of >95% (5%/2 mm) for all four targets. For our first 58 patients, film-based patient-specific quality assurance has resulted in an average %GP of 98.7% (range, 94-100%) at 2%/2 mm.

CONCLUSIONS

Core ZAP-X features were found to be functional. On the basis of our results, point-dose and planar measurements were in agreement with TPS calculations using multiple phantoms and setup geometries, validating the ZAP-X TPS beam model for clinical use.

摘要

目的

通过非剂量学、剂量学和端到端(E2E)测试来评估 ZAP-X 立体定向放射外科(SRS)系统的治疗计划系统(TPS)性能。

方法

使用已发表的指南开发了一套全面的 TPS 调试和验证测试。非剂量学验证测试包括信息传输、计算机断层扫描-磁共振(CT-MR)图像配准、结构/轮廓、几何形状、剂量工具和 CT 密度。剂量学验证包括在各种几何形状和射束排列下比较 TPS 和水箱/固体水测量值以及端到端(E2E)测试。使用 Lucy 体模中的电离室和 CyberKnife 头体模中的 Gafchromic EBT3 胶片进行患者特定的质量保证。RadCalc 用于独立验证监测单位。使用 RPC Gamma Knife 热释光剂量计(TLD)体模、MD Anderson SRS 头体模和 PseudoPatient 凝胶体模进行了额外的 E2E 测试,以进行独立的绝对剂量验证。

结果

具有已知平移和旋转偏移的 CT-MR 图像配准在容差内(<0.5×最大体素尺寸)。切片厚度和距离精度在 0.1mm 以内,体积精度在 0 到 0.11cm 以内。TPS 体积测量不确定度在 0.1 到 0.4cm 以内。在水模中用单个射束进行的电离室点剂量测量与 TPS 计算值的偏差在±4%以内,适用于直径为 10 至 25mm 的准直器,对于所有测量深度(7、50、100、150 和 200mm),直径为 7.5mm 的为±6%。在同质的固体水中,点剂量测量值与 7.5 至 25mm 的圆锥尺寸偏差在±4%以内。对于 1cm 高/低密度插件,测量值与直径为 10 至 25mm 的圆锥尺寸的偏差在±4.2%以内。使用 4/5mm 圆锥的基于胶片的 E2E 产生了 99.8%(2%/1.5mm)的伽马通过率(%GP)。使用分布在三个非共面弧上的 36 束射束的 Lucy 体模中的电离室点剂量测量值与直径为 10 至 25mm 的圆锥尺寸的偏差在±4%以内。RPC Gamma Knife TLD 体模的测量到预期 TLD 剂量比为 1.02,符合通过率结果。MD Anderson SRS 头体模的通过率结果为 4%的 TLD 一致性和 95%/93%(5%/3mm)的冠状/矢状面胶片平面的%GP。RTsafe 凝胶体模的所有四个目标的%GP 均>95%(5%/2mm)。对于我们的前 58 名患者,基于胶片的患者特定质量保证导致平均%GP 为 98.7%(范围为 94-100%),2%/2mm。

结论

核心 ZAP-X 功能被发现是有效的。基于我们的结果,点剂量和平面测量值与使用多个体模和设置几何形状的 TPS 计算值一致,验证了 ZAP-X TPS 射束模型的临床应用。

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