ZAP-X

ZAP - X
  • 文章类型: Journal Article
    目的:通过与两个成熟的SRS平台比较,评估ZAP-X立体定向放射外科(SRS)治疗单发脑转移瘤的剂量学特征。
    方法:回顾性选择13例接受Cyberknife(CK)G4治疗的单发脑转移患者。计划目标体积(PTV)的处方剂量为1-3分的18-24Gy。PTV体积范围从0.44到11.52cc。使用ZAP-X计划系统和伽玛刀(GK)ICON计划系统以相同的处方剂量和危险器官(OAR)约束对13名患者的治疗计划进行了重新检查。对于ZAP-X和CK,PTV的处方剂量均归一化为70%,而GK为50%。三组的剂量学参数包括计划特征(CI,GI,GSI,梁,MU,治疗时间),PTV(D2,D95,D98,Dmin,Dmean,覆盖范围),脑组织(体积100%-10%处方剂量照射V100%-V10%,Dmean)和其他OAR(Dmax,Dmean),对所有这些进行了比较和评价.读取所有数据并用MIMMaestro进行分析。进行了单因素方差分析或多样本弗里德曼秩和检验,其中p<0.05表示显著差异。
    结果:GK的TheCI明显低于ZAP-X和CK。关于平均值,ZAP-X的GI较低,GSI较高,但是三组之间没有显着差异。ZAP-X的MU明显低于CK,ZAP-X治疗时间的平均值明显短于CK。对于PTV,CK的D95、D98和目标覆盖率较高,GK的Dmin均值明显低于CK和ZAP-X。对于脑组织,ZAP-X显示从V100%到V20%的较小体积;V60%和V50%的统计结果显示ZAP-X和GK之间存在差异,而V40%和V30%在ZAP-X和其他两组之间显示显着差异;V10%和Dmean表明GK更好。不包括脑干的Dmax,右视神经和视交叉,所有其他OAR的平均值均小于1Gy。对于脑干,GK和ZAP-X有更好的保护,尤其是在最大剂量。
    结论:对于SRS治疗单发脑转移瘤,所有三个治疗装置,ZAP-X系统,CyberknifeG4系统,和GammaKnife系统,能满足临床治疗要求。新平台ZAP-X可以提供与赛波刀和伽玛刀相当甚至更好的高质量计划,ZAP-X具有一定的剂量优势,特别是具有更适形的剂量分布和更好的保护脑组织。随着ZAP-X系统的不断改进和升级,它们可能成为治疗脑转移瘤的新的SRS平台。
    OBJECTIVE: To evaluate the dosimetric characteristics of ZAP-X stereotactic radiosurgery (SRS) for single brain metastasis by comparing with two mature SRS platforms.
    METHODS: Thirteen patients with single brain metastasis treated with CyberKnife (CK) G4 were selected retrospectively. The prescription dose for the planning target volume (PTV) was 18-24 Gy for 1-3 fractions. The PTV volume ranged from 0.44 to 11.52 cc.Treatment plans of thirteen patients were replanned using the ZAP-X plan system and the Gamma Knife (GK) ICON plan system with the same prescription dose and organs at risk (OARs) constraints. The prescription dose of PTV was normalized to 70% for both ZAP-X and CK, while it was 50% for GK. The dosimetric parameters of three groups included the plan characteristics (CI, GI, GSI, beams, MUs, treatment time), PTV (D2, D95, D98, Dmin, Dmean, Coverage), brain tissue (volume of 100%-10% prescription dose irradiation V100%-V10%, Dmean) and other OARs (Dmax, Dmean),all of these were compared and evaluated. All data were read and analyzed with MIM Maestro. One-way ANOVA or a multisample Friedman rank sum test was performed, where p < 0.05 indicated significant differences.
    RESULTS: The CI of GK was significantly lower than that of ZAP-X and CK. Regarding the mean value, ZAP-X had a lower GI and higher GSI, but there was no significant difference among the three groups. The MUs of ZAP-X were significantly lower than those of CK, and the mean value of the treatment time of ZAP-X was significantly shorter than that of CK. For PTV, the D95, D98, and target coverage of CK were higher, while the mean of Dmin of GK was significantly lower than that of CK and ZAP-X. For brain tissue, ZAP-X showed a smaller volume from V100% to V20%; the statistical results of V60% and V50% showed a difference between ZAP-X and GK, while the V40% and V30% showed a significant difference between ZAP-X and the other two groups; V10% and Dmean indicated that GK was better. Excluding the Dmax of the brainstem, right optic nerve and optic chiasm, the mean value of all other OARs was less than 1 Gy. For the brainstem, GK and ZAP-X had better protection, especially at the maximum dose.
    CONCLUSIONS: For the SRS treating single brain metastasis, all three treatment devices, ZAP-X system, CyberKnife G4 system, and GammaKnife system, could meet clinical treatment requirements. The newly platform ZAP-X could provide a high-quality plan equivalent to or even better than CyberKnife and Gamma Knife, with ZAP-X presenting a certain dose advantage, especially with a more conformal dose distribution and better protection for brain tissue. As the ZAP-X systems get continuous improvements and upgrades, they may become a new SRS platform for the treatment of brain metastasis.
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  • 文章类型: Journal Article
    ZAP-X,一种新颖的专用放射外科(SRS)系统,最近出现了,在过去的二十年中,Cyberknife巩固了其作为SRS和立体定向身体放射治疗的通用解决方案的地位。本研究旨在比较ZAP-X和射波刀治疗不同靶点大小的脑转移瘤的剂量学性能和递送效率。采用圆形准直。
    23名患者,总共包括47个脑转移瘤,包括在ZAP-X和CyberKnife的比较计划的创建中进行分析。生成比较计划以实现相同的目标处方剂量,同时对危险器官(OAR)坚持相同的剂量限制。每个计划的处方等剂量百分比在97-100%的范围内进行优化,以确保有效的目标体积覆盖率。要评估计划质量,一致性等指标,同质性,和梯度(CI,HI,和GI)进行了计算,以及接收12Gy和10Gy的大脑总体积的报告。在评估分娩效率时,比较了两种模式之间估计的治疗时间和监测单位(MU)。
    总的来说,射波刀取得了更好的CI和HI,而ZAP-X对正常大脑表现出更好的GI和更小的照射体积。对于小于1cc和大于10cc的目标尺寸,赛波刀计划一致性的优越性更为明显。相反,ZAP-X计划剂量梯度的优势在10cc以下的靶大小更显著。ZAP-X计划的同质性,雇佣多个等中心,显示与目标的形状和计划者在放置等中心方面的经验有很强的相关性。一般来说,两种模式的估计治疗时间相似,并且递送效率受到两种模式的选择的准直尺寸的显著影响。
    这项研究表明,在患者队列中的目标大小范围内,ZAP-X和CyberKnife生成的计划具有可比的计划质量和交付效率。目前,在两种模式的当前平台下,Cyberknife在一致性和同质性方面优于ZAP-X,而ZAP-X倾向于产生剂量下降更快的计划。
    UNASSIGNED: ZAP-X, a novel and dedicated radiosurgery (SRS) system, has recently emerged, while CyberKnife has solidified its position as a versatile solution for SRS and stereotactic body radiation therapy over the past two decades. This study aims to compare the dosimetric performance and delivery efficiency of ZAP-X and CyberKnife in treating brain metastases of varying target sizes, employing circular collimation.
    UNASSIGNED: Twenty-three patients, encompassing a total of 47 brain metastases, were included in the creation of comparative plans of ZAP-X and CyberKnife for analysis. The comparative plans were generated to achieve identical prescription doses for the targets, while adhering to the same dose constraints for organs at risk (OAR). The prescription isodose percentage was optimized within the range of 97-100% for each plan to ensure effective target-volume coverage. To assess plan quality, indices such as conformity, homogeneity, and gradient (CI, HI, and GI) were computed, along with the reporting of total brain volumes receiving 12Gy and 10Gy. Estimated treatment time and monitor units (MUs) were compared between the two modalities in evaluating delivery efficiency.
    UNASSIGNED: Overall, CyberKnife achieved better CI and HI, while ZAP-X exhibited better GI and a smaller irradiated volume for the normal brain. The superiority of CyberKnife\'s plan conformity was more pronounced for target size less than 1 cc and greater than 10 cc. Conversely, the advantage of ZAP-X\'s plan dose gradient was more notable for target sizes under 10 cc. The homogeneity of ZAP-X plans, employing multiple isocenters, displayed a strong correlation with the target\'s shape and the planner\'s experience in placing isocenters. Generally, the estimated treatment time was similar between the two modalities, and the delivery efficiency was significantly impacted by the chosen collimation sizes for both modalities.
    UNASSIGNED: This study demonstrates that, within the range of target sizes within the patient cohort, plans generated by ZAP-X and CyberKnife exhibit comparable plan quality and delivery efficiency. At present, with the current platform of the two modalities, CyberKnife outperforms ZAP-X in terms of conformity and homogeneity, while ZAP-X tends to produce plans with a more rapid dose falloff.
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  • 文章类型: Journal Article
    放射外科和立体定向放射疗法已将自己确立为用于治疗脑和颅外病变的精确和准确的放射肿瘤学区域。随着其他放射治疗方法的发展,这种类型的治疗在提高治疗准确性和疗效的各种方式和技术方面取得了重大进展.本文全面概述了几十年来立体定向放射外科(SRS)的进展,包括对各种文章和研究论文的回顾,从立体定向技术在放射治疗中的出现开始。SRS的关键临床方面,如固定方法,放射生物学的考虑,质量保证实践,和治疗计划策略,被呈现。此外,审查强调了治疗模式的技术进步,涵盖从基于钴的系统到基于线性加速器的模式的过渡。通过解决这些问题,这项研究旨在提供对已经塑造了SRS领域的进步的见解,最终提高了治疗的准确性和有效性。
    Radiosurgery and stereotactic radiotherapy have established themselves as precise and accurate areas of radiation oncology for the treatment of brain and extracranial lesions. Along with the evolution of other methods of radiotherapy, this type of treatment has been associated with significant advances in terms of a variety of modalities and techniques to improve the accuracy and efficacy of treatment. This paper provides a comprehensive overview of the progress in stereotactic radiosurgery (SRS) over several decades, and includes a review of various articles and research papers, commencing with the emergence of stereotactic techniques in radiotherapy. Key clinical aspects of SRS, such as fixation methods, radiobiology considerations, quality assurance practices, and treatment planning strategies, are presented. In addition, the review highlights the technological advancements in treatment modalities, encompassing the transition from cobalt-based systems to linear accelerator-based modalities. By addressing these topics, this study aims to offer insights into the advancements that have shaped the field of SRS, that have ultimately enhanced the accuracy and effectiveness of treatment.
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  • 文章类型: Journal Article
    背景:放射外科是各种颅内肿瘤的公认治疗方法。与其他已建立的放射外科平台相比,新的ZAP-X®允许自屏蔽陀螺放射外科。这里,具有可变光束开启时间的治疗光束瞄准少量等中心。现有的规划框架依赖于基于随机选择或人工选择等中心的启发式,这通常会导致临床实践中更高的计划质量。
    目的:这项工作的目的是研究放射外科治疗计划的改进方法,它使用新系统ZAP-X®自动选择治疗头颈部脑肿瘤和疾病的等中心位置。
    方法:我们提出了一种自动获取等中心位置的新方法,这在陀螺放射外科治疗计划中是必不可少的。首先,基于随机选择的非等中心候选波束集创建最佳治疗方案。然后对所得到的加权波束子集的交点进行聚类以找到等中心。这种方法与球体填充相比,随机选择,并由专家计划者选择生成等中心。我们回顾性评估10例听神经瘤的计划质量。
    结果:通过聚类方法获得的等中心结果为所有10个测试案例的临床可行计划。当使用相同数量的等中心时,与随机选择相比,聚类方法平均将覆盖率提高了31个百分点,与球体包装相比有15个百分点,与专家选择的等中心获得的覆盖率相比有2个百分点。自动确定等中心引线的位置和数量,平均而言,覆盖率为97±3%,一致性指数为1.22±0.22,而使用的等中心比手动选择的少2.46±3.60。在算法性能方面,所有计划均在不到2分钟的时间内计算,平均运行时间为75±25s。
    结论:这项研究证明了在使用ZAP-X®系统的治疗计划过程中通过聚类进行自动等中心选择的可行性。即使在现有方法无法产生可行计划的复杂情况下,聚类方法产生的计划与专家选择的等中心产生的计划相当。因此,我们的方法可以帮助减少陀螺放射外科治疗计划所需的工作量和时间.
    BACKGROUND: Radiosurgery is a well-established treatment for various intracranial tumors. In contrast to other established radiosurgery platforms, the new ZAP-X® allows for self-shielding gyroscopic radiosurgery. Here, treatment beams with variable beam-on times are targeted towards a small number of isocenters. The existing planning framework relies on a heuristic based on random selection or manual selection of isocenters, which often leads to a higher plan quality in clinical practice.
    OBJECTIVE: The purpose of this work is to study an improved approach for radiosurgery treatment planning, which automatically selects the isocenter locations for the treatment of brain tumors and diseases in the head and neck area using the new system ZAP-X® .
    METHODS: We propose a new method to automatically obtain the locations of the isocenters, which are essential in gyroscopic radiosurgery treatment planning. First, an optimal treatment plan is created based on a randomly selected nonisocentric candidate beam set. The intersections of the resulting subset of weighted beams are then clustered to find isocenters. This approach is compared to sphere-packing, random selection, and selection by an expert planner for generating isocenters. We retrospectively evaluate plan quality on 10 acoustic neuroma cases.
    RESULTS: Isocenters acquired by the method of clustering result in clinically viable plans for all 10 test cases. When using the same number of isocenters, the clustering approach improves coverage on average by 31 percentage points compared to random selection, 15 percentage points compared to sphere packing and 2 percentage points compared to the coverage achieved with the expert selected isocenters. The automatic determination of location and number of isocenters leads, on average, to a coverage of 97 ± 3% with a conformity index of 1.22 ± 0.22, while using 2.46 ± 3.60 fewer isocenters than manually selected. In terms of algorithm performance, all plans were calculated in less than 2 min with an average runtime of 75 ± 25 s.
    CONCLUSIONS: This study demonstrates the feasibility of an automatic isocenter selection by clustering in the treatment planning process with the ZAP-X® system. Even in complex cases where the existing approaches fail to produce feasible plans, the clustering method generates plans that are comparable to those produced by expert selected isocenters. Therefore, our approach can help reduce the effort and time required for treatment planning in gyroscopic radiosurgery.
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  • 文章类型: Journal Article
    ZAP-X代表了同类中的第一个“自屏蔽”治疗放射装置,由于新奇,挑战监管机构将其纳入现有的辐射防护监管框架。为了促进知情的监管解释,在患者和X射线靶平面的水平处,在屏蔽治疗胶囊内部测量来自ZAP-X的X射线辐射泄漏。在针对参考条件校准的临床调试系统上进行测量以递送1cGy/MU。用FLUKE451测量仪和RadCal电离室测量辐射作为暴露量和剂量,并以系统参考剂量的百分比表示。在十三个地点进行了测量,患者平面中有8个,X射线目标平面中有5个。结果显示,患者平面中的最大X射线泄漏为0.000986%,目标平面中的最大X射线泄漏为0.000907%。这些结果比用于放射治疗直线加速器(LINAC)的IEC指南标准60601-2-1(2020)所引用的现有建议低30-100倍。尽管大多数传统的LINAC将2-5的安全系数应用于准直器屏蔽和患者剂量节约的设计,与该标准相比,ZAP-X提供的患者全身剂量不到10%,来自X射线目标。尽管ZAP-X调强放射治疗(IMRT)因子明显高于传统的Linacs,来自泄漏辐射的绝对剂量仍然低25。从临床和放射安全性的角度来看,患者身体远离等中心的非预期剂量是令人感兴趣的。随着全身剂量的减少,由此导致的与治疗相关的癌症发病率和死亡率相应降低。
    The ZAP-X represents the first-of-its-kind \"self-shielded\" therapeutic radiation device, which by novelty, challenges regulators to accommodate it within the existing regulatory framework for radiation protection. To facilitate informed regulatory interpretation, X-ray radiation leakage from the ZAP-X was measured inside the shielded treatment capsule at the level of the patient and X-ray target plane. Measurements were performed on a clinically commissioned system calibrated for reference conditions to deliver 1cGy/MU. Radiation was measured with a FLUKE 451 survey meter and a RadCal ionization chamber as both exposure and dose and presented as a percentage of the system reference dose. Measurements were taken at thirteen locations, eight in the patient plane and five in the X-ray target plane. The results showed a maximum X-ray leakage of 0.000986% in the patient plane and 0.000907% in the target plane. These results are 30 - 100 times lower than existing recommendations as referenced by IEC guidelines standard 60601-2-1 (2020) for radiotherapy linear accelerators (LINACs). Although most conventional LINACs apply a safety factor of 2-5 to the design of collimator shielding and patient dose sparing, the ZAP-X delivers less than 10% of the patient whole body dose compared to this standard, originating from the X-ray target. Even though the ZAP-X intensity modulated radiation therapy (IMRT) factor is significantly higher than conventional Linacs, the absolute dose originating from leakage radiation remains lower by 25. The amount of unintended dose received by the patient\'s body distant from the isocenter is of interest from the perspective of both clinical and radiation safety. As this whole-body dose is decreased, the resulting treatment-related cancer incidence and mortality rates are decreased accordingly.
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  • 文章类型: Journal Article
    This study provides insight into the overall system performance, stability, and delivery accuracy of the first clinical self-shielded stereotactic radiosurgery (SRS) system. Quality assurance procedures specifically developed for this unit are discussed, and trends and variations over the course of 2-years for beam constancy, targeting and dose delivery are presented. Absolute dose calibration for this 2.7 MV unit is performed to deliver 1 cGy/MU at dmax  = 7 mm at a source-to-axis-distance (SAD) of 450 mm for a 25 mm collimator. Output measurements were made with 2-setups: a device that attaches to a fixed position on the couch (daily) and a spherical phantom that attaches to the collimating wheel (monthly). Beam energy was measured using a cylindrical acrylic phantom at depths of 100 (D10 ) and 200 (D20 ) mm. Beam profiles were evaluated using Gafchromic film and compared with TPS beam data. Accuracy in beam targeting was quantified with the Winston-Lutz (WL) and end-to-end (E2E) tests. Delivery quality assurance (DQA) was performed prior to clinical treatments using Gafchromic EBT3/XD film. Net cumulative output adjustments of 15% (pre-clinical), 9% (1st year) and 3% (2nd year) were made. The mean output was 0.997 ± 0.010 cGy/MU (range: 0.960-1.046 cGy/MU) and 0.993 ± 0.029 cGy/MU (range: 0.884-1.065 cGy/MU) for measurements with the daily and monthly setups, respectively. The mean relative beam energy (D10 /D20 ) was 0.998 ± 0.004 (range: 0.991-1.006). The mean total targeting error was 0.46 ± 0.17 mm (range: 0.06-0.98 mm) for the WL and 0.52 ± 0.28 mm (range: 0.11-1.27 mm) for the E2E tests. The average gamma pass rates for DQA measurements were 99.0% and 90.5% for 2%/2 mm and 2%/1 mm gamma criteria, respectively. This SRS unit meets tolerance limits recommended by TG-135, MPPG 9a., and TG-142 with a treatment delivery accuracy similar to what is achieved by other SRS systems.
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  • 文章类型: Journal Article
    背景:准确的绝对剂量(AD)校准方法对于放射治疗机的正常运行至关重要。许多系统不符合TG-51校准标准,和修改是必需的。TG-21校准也是适用于这些情况的可行方法,设备,和因素。已经表明,这两种方法都导致最小的误差。在校准最近的无拱顶放射外科系统的剂量时,已经采取了类似的方法。
    目的:为了评估使用离子室对ZAP-X放射外科系统进行AD校准的改良TG-21和TG-51方案,电影,和热释光剂量计(TLD)。
    方法:ZAP-X的当前治疗计划系统需要在dmax(7mm)和450mm的源到轴距离进行AD校准。两个ND,w60Co[Gy/C]$N_{D,w}^{{60}Co}[{Gy/C}]$和Nx[R/C]校准系数由认可的剂量学校准实验室提供,用于物理检验技术(PTW)31010室(0.125cc)。供应商提供了可以安装在准直器上的f形支架。然后可以将各种体模附接到f形支架。根据TG-21和技术报告系列-398的建议设计了一个定制的丙烯酸体模,该腔室距离源头500毫米,深度为44毫米丙烯酸和456毫米SSD。Nx与其他TG-21参数一起用于计算AD。使用PTWMP3-XS水箱和相同腔室进行的测量用于使用ND计算AD,w60Co$N_{D,w}^{{60}Co}$和TG-51因素。使用Gafchrome胶片和第三方TLD进行剂量验证。
    结果:来自TG-51,TG-21(使用定制丙烯酸体模)的测量值,电影,和TLD同意在±2%以内。
    结论:在水中进行改进的TG-51AD计算是优选的,但由于储罐设置困难,可能不切实际。使用定制丙烯酸体模的TG-21修改方案是剂量校准的准确替代选择。这两种方法均在可接受的协议范围内,并对系统的AD校准提供了信心。
    BACKGROUND: Methods for accurate absolute dose (AD) calibration are essential for the proper functioning of radiotherapy treatment machines. Many systems do not conform to TG-51 calibration standards, and modifications are required. TG-21 calibration is also a viable methodology for these situations with the appropriate setup, equipment, and factors. It has been shown that both these methods result in minimal errors. A similar approach has been taken in calibrating the dose for a recent vault-free radiosurgery system.
    OBJECTIVE: To evaluate modified TG-21 and TG-51 protocols for AD calibrations of the ZAP-X radiosurgery system using ion chambers, film, and thermoluminescent dosimeters (TLDs).
    METHODS: The current treatment planning system for ZAP-X requires AD calibration at dmax (7 mm) and 450 mm source-to-axis distance. Both N D , w 60 C o [ G y / C ] $N_{D,w}^{{60}Co}[ {Gy/C} ]$ and Nx [R/C] calibration coefficients were provided by an accredited dosimetry calibration laboratory for a physikalisch technische werkstatten (PTW) 31010 chamber (0.125 cc). The vendor provides an f-bracket that can be mounted on the collimator. Various phantoms can then be attached to the f-bracket. A custom acrylic phantom was designed based on recommendations from TG-21 and technical report series-398 that places the chamber at 500 mm from the source with a depth of 44-mm acrylic and 456-mm SSD. Nx along with other TG-21 parameters was used to calculate the AD. Measurements using a PTW MP3-XS water tank and the same chamber were used to calculate AD using N D , w 60 C o $N_{D,w}^{{60}Co}$ and TG-51 factors. Dose verification was performed using Gafchromic film and 3rd party TLDs.
    RESULTS: Measurements from TG-51, TG-21 (utilizing the custom acrylic phantom), film, and TLDs agreed to within ± 2%.
    CONCLUSIONS: A modified TG-51 AD calculation in water is preferred but may not be practical due to the difficulty in tank setup. The TG-21 modified protocol using a custom acrylic phantom is an accurate alternative option for dose calibration. Both of these methods are within acceptable agreement and provide confidence in the system\'s AD calibration.
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  • 文章类型: Journal Article
    自屏蔽陀螺放射外科(GRS)代表了立体定向放射外科领域的技术创新。GRS不需要放射拱顶,并且针对放射外科治疗进行了优化。有关其使用情况的报告有限。我们描述了GRS在我们机构的首次临床经验,以评估GRS在颅骨肿瘤治疗中的应用。此外,我们对机器人放射外科(RRS)与前庭神经鞘瘤(VS)GRS患者进行了剂量学比较。
    包括2021年7月至11月间接受GRS治疗的患者。病人,肿瘤,并对剂量学特点进行回顾性总结和分析。
    纳入41例颅内肿瘤患者48例。肿瘤实体主要包括VS,脑转移瘤,和脑膜瘤.良性肿瘤的中位处方剂量和等剂量线为13.5Gy和50.0%,恶性肿瘤为20Gy和60.0%,分别。平均计划目标体积为1.5立方厘米。所有患者都接受了单次治疗,没有遇到任何技术设置困难。治疗计划与RRS比较显示出可比的计划特征,剂量梯度,和处于危险剂量的器官。在新的符合性指数和每次治疗的监测单位数方面发现了显着差异(均P<0.01)。
    本系列病例提供了更多关于在颅骨肿瘤治疗中使用自屏蔽GRS的证据。VS病例的剂量学比较显示出与RRS几乎相等的剂量学特征。GRS的进一步临床和物理分析正在进行中。
    Self-shielding gyroscopic radiosurgery (GRS) represents a technical innovation in the field of stereotactic radiosurgery. GRS does not require a radiation vault and is optimized for radiosurgical treatments. Reports on its usage are limited. We describe the first clinical experience of GRS at our institution to assess the application of GRS in the treatment of cranial tumors. Moreover, we perform a dosimetric comparison to robotic radiosurgery (RRS) with vestibular schwannoma (VS) GRS patients.
    Patients who were treated with GRS between July and November 2021 were included. Patient, tumor, and dosimetric characteristics were retrospectively summarized and analyzed.
    Forty-one patients with 48 intracranial tumors were included. Tumor entities mostly comprised VS, brain metastases, and meningiomas. The median prescription dose and isodose line were 13.5 Gy and 50.0% for benign neoplasia versus 20 Gy and 60.0% for malignant tumors, respectively. The mean planning target volume was 1.5 cubic centimeters. All patients received a single-fraction treatment without encountering any technical setup difficulties. Treatment plan comparisons with RRS revealed comparable plan characteristics, dose gradients, and organs at risk doses. Significant differences were detected concerning the new conformity index and number of monitor units per treatment (both P < 0.01).
    This case series provides more evidence on the usage of self-shielding GRS in the management of cranial tumors. Dosimetric comparisons for VS cases revealed mostly equivalent dosimetric characteristics to RRS. Further clinical and physical analyses for GRS are underway.
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  • 文章类型: Journal Article
    OBJECTIVE: This study reports a single-institution experience with beam data acquisition and film-based validation for a novel self-shielded sterotactic radiosurgery unit and investigates detector dependency on field output factors (OFs), off-axis ratios (OARs), and percent depth dose (PDD) measurements within the context of small-field dosimetry.
    METHODS: The delivery platform for this unit consists of a 2.7-MV S-band linear accelerator mounted on coupled gimbals that rotate around a common isocenter (source-to-axis distance [SAD] = 450 mm), allowing for more than 260 noncoplanar beam angles. Beam collimation is achieved via a tungsten collimator wheel with eight circular apertures ranging from 4 mm to 25 mm in diameter. Three diodes (PTW 60012 Diode E, PTW 60018 SRS Diode, and Sun Nuclear EDGE) and a synthetic diamond detector (PTW 60019 micro Diamond [µD] detector) were used for OAR, PDD, and OF measurements. OFs were also acquired with a PTW 31022 PinPoint ionization chamber. Beam scanning was performed using a 3D water tank at depths of 7, 50, 100, 200, and 250 mm with a source-to-surface distance of 450 mm. OFs were measured at the depth of maximum dose (dmax  = 7 mm) with the SAD at 450 mm. Gafchromic EBT3 film was used to validate OF and profile measurements and as a reference detector for estimating correction factors for active detector OFs. Deviations in field size, penumbra, and PDDs across the different detectors were quantified.
    RESULTS: Relative OFs (ROFs) for the diodes were within 1.4% for all collimators except for 5 and 7.5 mm, for which SRS Diode measurements were higher by 1.6% and 2.6% versus Diode E. The µD ROFs were within 1.4% of the diode measurements. PinPoint ROFs were lower by >10% for the 4-mm and 5-mm collimators versus the Diode E and µD. Corrections to OFs using EBT3 film as a reference were within 1.2% for all diodes and the µD detector for collimators 10 mm and greater and within 2.0%, 2.8%, and 1.1% for the 7.5-, 5-, and 4-mm collimators, respectively. The maximum difference in full width at half maximum (FWHM) between the Diode E and the other active detectors was for the 25-mm collimator and was 0.09 mm (µD), 0.16 mm (SRS Diode), and 0.65 mm (EDGE). Differences seen in PDDs beyond the depth of dmax were <1% across the three diodes and the µD. FWHM and penumbra measurements made using EBT3 film were within 1.34% and 3.26%, respectively, of the processed profile data entered into the treatment planning system.
    CONCLUSIONS: Minimal differences were seen in OAR and PDD measurements acquired with the diodes and the µD. ROFs measured with the three diodes were within 2.6% and within 1.4% versus the µD. Gafchromic Film measurements provided independent verification of the OAR and OF measurements. Estimated corrections to OFs using film as a reference were <1.6% for the Diode E, EDGE, and µD detector.
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  • 文章类型: Letter
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