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Reduction of radiation dose to the eye lens during common CT examinations of the head, paranasal sinus, and cervical spine in emergency settings: A phantom study. 急诊情况下头部、副鼻窦和颈椎普通CT检查时对晶状体的辐射剂量降低:一项幻象研究
IF 2.2 4区 医学 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2026-02-01 DOI: 10.1002/acm2.70486
Sowitchaya Huakham, Wirachad Sripoori, Raksumon Suksi, Thawatchai Thaikan, Thanyawee Pengpan

Background: Computed tomography (CT) examinations of the head, paranasal sinus (PNS), and cervical spine (C-spine) are frequently performed in emergency settings, raising concerns about radiation exposure to the radiosensitive eye lens. Overexposure can cause radiation-induced ocular damage. To address this concern, organ dose modulation (ODM) has emerged as a promising technique for reducing eye lens dose in CT examinations.

Purpose: This study aimed to evaluate radiation exposure to the eye lens and objective image quality metrics for head, PNS, and C-spine CT examinations using fixed tube current, automatic tube current modulation (ATCM), and ODM techniques.

Methods: Eye lens doses were measured using nanoDot optically stimulated luminescence dosimeters (OSLDs) placed bilaterally to the eye lens of a whole-body anthropomorphic phantom (PBU-60). CT scans were performed using a Revolution EX CT scanner with three scanning techniques: fixed tube current, ATCM, and ODM. The phantom was scanned twice for each examination type (head, PNS, and C-spine) with all three techniques. Eye lens dose reductions with the ODM technique were quantified relative to fixed tube current and ATCM techniques. Image quality was quantitatively evaluated in terms of image noise, signal-to-noise ratio (SNR), and contrast-to-noise ratio (CNR).

Results: Mean eye lens doses ± standard deviation (SD) using the ODM technique were 38.44 ± 1.37, 17.92 ± 1.01, and 9.77 ± 0.38 mGy for head, PNS, and C-spine, respectively. These eye lens doses were reduced by 4.28%, 21.33%, and 47.97% compared to the fixed tube current techniques and by 19.40%, 24.70%, and 13.69% compared to the ATCM techniques, for head, PNS, and C-spine, respectively. These dose reductions were achieved while maintaining image quality metrics (image noise, SNR, and CNR) with no statistically significant differences (p > 0.05) compared to fixed tube current and ATCM techniques.

Conclusion: Implementation of the ODM technique resulted in significant eye lens dose reduction (4.28%-47.97%) across head, PNS, and C-spine CT examinations with no significant differences in image noise, SNR, and CNR compared to both fixed tube current and ATCM techniques. ODM demonstrates potential as a practical dose optimization strategy for routine emergency head and neck CT imaging. Further studies with subjective image quality assessment are recommended to evaluate clinical diagnostic acceptability in hospital settings.

背景:头部、副鼻窦(PNS)和颈椎(C-spine)的计算机断层扫描(CT)检查经常在紧急情况下进行,这引起了对辐射敏感眼晶状体辐射暴露的担忧。过度暴露会引起辐射引起的眼部损伤。为了解决这一问题,器官剂量调节(ODM)已经成为一种很有前途的技术,用于减少CT检查中的晶状体剂量。目的:本研究旨在评估使用固定管电流、自动管电流调制(ATCM)和ODM技术进行头部、PNS和颈椎CT检查时,眼晶状体的辐射暴露和客观图像质量指标。方法:采用纳米点光刺激发光剂量计(osld)测量眼晶状体剂量,该剂量计放置在全身拟人幻影(PBU-60)的眼晶状体两侧。CT扫描使用Revolution EX CT扫描仪,采用三种扫描技术:固定管电流、ATCM和ODM。采用所有三种技术对每个检查类型(头部、PNS和颈椎)的幻肢进行两次扫描。相对于固定管电流和ATCM技术,对ODM技术的眼晶状体剂量减少量进行了量化。通过图像噪声、信噪比(SNR)和噪声对比比(CNR)对图像质量进行定量评价。结果:使用ODM技术,头部、PNS和颈椎的平均晶状体剂量±标准差(SD)分别为38.44±1.37、17.92±1.01和9.77±0.38 mGy。与固定管电流技术相比,这些眼球晶状体剂量分别减少4.28%、21.33%和47.97%,与ATCM技术相比,头部、PNS和颈椎的晶状体剂量分别减少19.40%、24.70%和13.69%。与固定管电流和ATCM技术相比,在保持图像质量指标(图像噪声、信噪比和CNR)的同时实现了这些剂量的降低,没有统计学上的显著差异(p > 0.05)。结论:与固定管电流和ATCM技术相比,ODM技术的实施使头部、PNS和颈椎CT检查的晶体剂量显著降低(4.28%-47.97%),图像噪声、信噪比和CNR无显著差异。ODM显示了作为常规急诊头颈部CT成像的实用剂量优化策略的潜力。建议进一步研究主观图像质量评估,以评估医院设置的临床诊断可接受性。
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引用次数: 0
RapidArc Dynamic (RAD) multi-mechanical axis optimization achieves enhanced OAR sparing in cervical cancer: A dosimetric comparison study. RapidArc动态(RAD)多机械轴优化实现增强子宫颈OAR保留:剂量学比较研究。
IF 2.2 4区 医学 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2026-02-01 DOI: 10.1002/acm2.70506
Xiangyin Meng, Zhiqun Wang, Yiming Zhang, Xingliu Wang, Xiaoshen Wang, Weihua Zhu, Fuqiang Chen, Zhen Zhang, Fengchao Xu, Zhufeng Wu, Bo Yang, Jie Qiu
<p><strong>Purpose: </strong>To overcome limitations of conventional VMAT for cervical cancer, specifically restricted OAR sparing due to static collimators and delivery constraints inherent to dynamic modulation, we systematically evaluate RapidArc Dynamic (RAD) technology. This first comprehensive assessment focuses on RAD's multi-axis coordination for optimized pelvic radiotherapy planning.</p><p><strong>Methods: </strong>Twenty cervical cancer patients treated with TrueBeam whose energy was 6MV X-ray were retrospectively analyzed. The prescription was 45 Gy/25Fractions. Seven RAD-based planning strategies with varying collimator rotation modes (Optimize [OPT] vs. Optimize Between Static Angles [OBSA] vs. Static [STAT]) and aperture sizes (15 vs. 30 cm) and different static angle ports were developed using identical optimization objectives. Re-optimized clinical plan using Eclipse v18.1. All RAD and clinical plans were normalized so that the target received a certain dose with 95% target coverage for final dosimetric comparison. Dosimetric comparisons employed ANOVA (with LSD post hoc) for parametric data or Kruskal-Wallis's test (with Mann-Whitney U post hoc) for non-parametric data, with significance set at p < 0.05.</p><p><strong>Results: </strong>RAD plans showed slightly inferior conformity and homogeneity compared to clinical plans, they achieved superior dose fall-off gradients. RAD's advantage was particularly evident in sparing organs at risk (OARs). Specifically, for the bladder, significant reductions were noted in <math> <semantics><msub><mi>D</mi> <mrow><mi>m</mi> <mi>e</mi> <mi>a</mi> <mi>n</mi></mrow> </msub> <annotation>${{D}_{mean}}$</annotation></semantics> </math> (8.29%-13.05%), <math> <semantics><msub><mi>V</mi> <mrow><mn>20</mn> <mrow><mspace></mspace> <mi>Gy</mi></mrow> </mrow> </msub> <annotation>${{V}_{20{mathrm{ Gy}}}}$</annotation></semantics> </math> (4.04%-26.71%), and <math> <semantics><msub><mi>V</mi> <mrow><mn>30</mn> <mrow><mspace></mspace> <mi>Gy</mi></mrow> </mrow> </msub> <annotation>${{V}_{30{mathrm{ Gy}}}}$</annotation></semantics> </math> (26.98%-32.46%) compared to the clinical plans. Similarly, for the rectum, reductions in <math> <semantics><msub><mi>D</mi> <mrow><mi>m</mi> <mi>e</mi> <mi>a</mi> <mi>n</mi></mrow> </msub> <annotation>${{D}_{mean}}$</annotation></semantics> </math> (9.21%-15.58%), <math> <semantics><msub><mi>V</mi> <mrow><mn>20</mn> <mrow><mspace></mspace> <mi>Gy</mi></mrow> </mrow> </msub> <annotation>${{V}_{20{mathrm{ Gy}}}}$</annotation></semantics> </math> (5.03%-14.77%), <math> <semantics><msub><mi>V</mi> <mrow><mn>30</mn> <mrow><mspace></mspace> <mi>Gy</mi></mrow> </mrow> </msub> <annotation>${{V}_{30{mathrm{ Gy}}}}$</annotation></semantics> </math> (18.24%-28.11%), and <math> <semantics><msub><mi>V</mi> <mrow><mn>40</mn> <mrow><mspace></mspace> <mi>Gy</mi></mrow> </mrow> </msub> <annotation>${{V}_{40{mathrm{ Gy}}}}$</annotation></semantics> </math> (23.73%-31.22%) were observed. O
目的:为了克服传统VMAT治疗宫颈癌的局限性,特别是由于静态准直器和动态调制固有的传输限制而限制了OAR的保留,我们系统地评估了RapidArc dynamic (RAD)技术。首次综合评估侧重于RAD的多轴协调以优化盆腔放疗计划。方法:对20例应用能量为6MV的TrueBeam治疗宫颈癌的患者进行回顾性分析。处方为45 Gy/25Fractions。使用相同的优化目标,开发了7种基于rad的规划策略,包括不同准直器旋转模式(优化[OPT] vs.优化静态角度[OBSA] vs.静态[STAT])、孔径大小(15 cm vs. 30 cm)和不同的静态角端口。使用Eclipse v18.1重新优化临床计划。所有RAD和临床计划均归一化,使目标接受一定剂量,目标覆盖率为95%,用于最终剂量学比较。剂量学比较对参数数据采用方差分析(采用LSD事后分析),对非参数数据采用Kruskal-Wallis检验(采用Mann-Whitney U事后分析),显著性设置为p。结果:与临床计划相比,RAD计划的符合性和均匀性略差,它们获得了更好的剂量衰减梯度。RAD的优势在保留危险器官(OARs)方面尤为明显。具体而言,与临床计划相比,膀胱的D mean ${D}_{mean}}$(8.29%-13.05%)、V 20 Gy ${V}_{20 mathrm{ Gy}}}}$(4.04%-26.71%)和V 30 Gy ${V}_{30 mathrm{ Gy}}}}$(26.98%-32.46%)显著降低。同样,直肠,减少D m e n $ {{D} _{意味着}}$ (9.21% - -15.58%),V 20 Gy $ {{V} _ {20 { mathrm { Gy}}}} $ (5.03% - -14.77%), V 30 Gy $ {{V} _ {30 { mathrm { Gy}}}} $(18.24% - -28.11%)和V 40 Gy $ {{V} _ {40 { mathrm { Gy}}}} $(23.73% - -31.22%)。其他桨也受益于改进的剂量学参数。虽然2ARC+OBSA+15和2ARC+STAT+15方案都优于其他RAD配置,但2ARC+OBSA+15方案通常提供更好的结果。值得注意的是,尽管RAD方案总体上显示小肠D2cc显著较高,但2ARC+OBSA+15方案的剂量与临床方案相当。在监控单元(MU)和计划复杂性方面,RAD计划更复杂,但保持了超过97%的高验证通过率。结论:RAD方案的初步探索显示出其在节省桨叶剂量方面的优势。此外,在RAD方案中,准直角度和孔径在15 cm处的优化获得了更好的剂量学结果。因此,进一步探索不同的机械轴组合对今后的研究具有重要意义。
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引用次数: 0
Acceptance testing of a 0.35 T MR-Linac: procedures, QA baseline, and system limitations. 0.35 T MR-Linac的验收测试:程序、QA基线和系统限制。
IF 2.2 4区 医学 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2026-02-01 DOI: 10.1002/acm2.70488
Mateb Al Khalifa, Tianjun Ma, Haya Aljuaid, Siyong Kim, William Y Song

Purpose: This study describes and evaluates the acceptance procedure for a ViewRay (VR) MRIdian 0.35T MR-Linac, emphasizing key challenges, limitations, and recommendations to enhance clinical performance and accuracy.

Methods: A comprehensive acceptance test was conducted at a single institution, following the manufacturer's protocols and aligned with established acceptance guidelines. Specific tools and phantoms were used to assess three primary components: mechanical, dosimetric, and Magnetic Resonance Imaging (MRI).

Results: Overall, the test outcomes satisfied the manufacturer's specifications. However, certain issues were identified: high couch attenuation at specific gantry angles (leading to their exclusion from treatment), variations in magnetic field homogeneity at different gantry angles, and discrepancies between TPS calculations and measurements for field output factors smaller than 0.83 cm × 0.83 cm.

Conclusion: This work provides a detailed account of the acceptance testing procedure and establishes a QA baseline for 0.35T MR-Linac systems. In doing so, it also identifies key system limitations, such as couch attenuation, magnetic field inhomogeneity, and small-field output discrepancies, underscoring the need for careful gantry angle selection, field homogeneity optimization, and meticulous validation of very small fields.

目的:本研究描述并评估了ViewRay (VR) mrridian 0.35T MR-Linac的接受程序,强调了关键的挑战、限制和建议,以提高临床表现和准确性。方法:在单一机构进行全面验收测试,遵循制造商的协议,并与既定的验收指南保持一致。使用特定的工具和模型来评估三个主要组成部分:机械,剂量学和磁共振成像(MRI)。结果:总体而言,测试结果满足制造商的规格。然而,也发现了一些问题:特定龙门架角度下的高沙发衰减(导致其被排除在处理之外),不同龙门架角度下磁场均匀性的变化,以及小于0.83 cm × 0.83 cm的场输出因子的TPS计算与测量之间的差异。结论:这项工作提供了验收测试程序的详细说明,并建立了0.35T MR-Linac系统的QA基线。在此过程中,它还确定了关键的系统限制,例如couch衰减,磁场不均匀性和小场输出差异,强调需要仔细选择龙门角度,场均匀性优化以及对非常小的场进行细致的验证。
{"title":"Acceptance testing of a 0.35 T MR-Linac: procedures, QA baseline, and system limitations.","authors":"Mateb Al Khalifa, Tianjun Ma, Haya Aljuaid, Siyong Kim, William Y Song","doi":"10.1002/acm2.70488","DOIUrl":"10.1002/acm2.70488","url":null,"abstract":"<p><strong>Purpose: </strong>This study describes and evaluates the acceptance procedure for a ViewRay (VR) MRIdian 0.35T MR-Linac, emphasizing key challenges, limitations, and recommendations to enhance clinical performance and accuracy.</p><p><strong>Methods: </strong>A comprehensive acceptance test was conducted at a single institution, following the manufacturer's protocols and aligned with established acceptance guidelines. Specific tools and phantoms were used to assess three primary components: mechanical, dosimetric, and Magnetic Resonance Imaging (MRI).</p><p><strong>Results: </strong>Overall, the test outcomes satisfied the manufacturer's specifications. However, certain issues were identified: high couch attenuation at specific gantry angles (leading to their exclusion from treatment), variations in magnetic field homogeneity at different gantry angles, and discrepancies between TPS calculations and measurements for field output factors smaller than 0.83 cm × 0.83 cm.</p><p><strong>Conclusion: </strong>This work provides a detailed account of the acceptance testing procedure and establishes a QA baseline for 0.35T MR-Linac systems. In doing so, it also identifies key system limitations, such as couch attenuation, magnetic field inhomogeneity, and small-field output discrepancies, underscoring the need for careful gantry angle selection, field homogeneity optimization, and meticulous validation of very small fields.</p>","PeriodicalId":14989,"journal":{"name":"Journal of Applied Clinical Medical Physics","volume":"27 2","pages":"e70488"},"PeriodicalIF":2.2,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12906295/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146194577","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
In-Silico Trial of Same-Day Simulation-Free Spatially Fractionated Adaptive Radiotherapy (SF2-ART). 当日无模拟的空间分割自适应放射治疗(SF2-ART)的计算机试验。
IF 2.2 4区 医学 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2026-02-01 DOI: 10.1002/acm2.70517
Dennis N Stanley, Alyssa R Birchmeier, Carlos E Cardenas, Richard A Popple, Natalie Viscariello, Joel A Pogue, Courtney B Stanley, Mehran Yusuf, Michael Soike, Samuel R Marcrom, Joseph Harms

Purpose: Here we present an in-silico trial of the feasibility and deliverability of a same-day, simulation-free workflow for spatially fractionated adaptive radiotherapy (SF2-ART) using the Varian Ethos platform.

Methods and materials: Ten patients (five thoracic and five extremity), previously treated with spatially fractionated radiotherapy (SFRT), were selected for this in silico trial. A two-phase regimen was simulated: Phase 1 delivered 12 Gy SBRT to a uniform, predefined high-dose lattice and 4 Gy to the gross tumor volume (GTV); Phase 2 consisted of 4 additional fractions of 4 Gy to the GTV. The planning workflow was performed entirely in silico, without the need for CT simulation. High-dose sphere matrices were generated with a custom script and aligned to physician-defined GTVs. Adaptive plans were created based on CBCT anatomy and evaluated for dosimetric quality, deliverability, and workflow timing. Comparisons were made to the original clinically delivered plans. Mobius3D was used for secondary dose verification.

Results: All 10 cases were successfully replanned using the SF2-ART workflow without simulation-based imaging. The entire planning and treatment process, including consultation, contouring, adaptive plan generation, and QA, was performed within a single session. Dosimetric comparisons showed minimal differences between simulation-free adaptive and clinically delivered plans, with target coverage and normal tissue constraints maintained across all cases. Median total estimated workflow time was 166.4 min.

Conclusions: This in-silico study demonstrates the feasibility of delivering spatially fractionated SBRT without simulation CT using a same-day adaptive workflow. The SF2-ART approach may enable rapid, high-quality treatment for patients with urgent or symptomatic presentations and supports future prospective clinical implementation.

目的:在这里,我们提出了一项利用Varian Ethos平台进行空间分割自适应放疗(SF2-ART)当日无模拟工作流程的可行性和可交付性的计算机试验。方法和材料:选择10例(5例胸部和5例四肢)先前接受过空间分割放疗(SFRT)的患者进行这项硅试验。模拟了两期方案:第一阶段将12 Gy的SBRT输送到均匀的、预定义的高剂量晶格,并将4 Gy输送到总肿瘤体积(GTV);第2阶段包括4个额外的4gy到GTV的馏分。规划工作流程完全在计算机上完成,不需要CT模拟。使用自定义脚本生成高剂量球体矩阵,并与医生定义的gtv对齐。根据CBCT解剖创建适应性计划,并评估剂量学质量、可交付性和工作流程时间。与最初的临床交付计划进行比较。使用Mobius3D进行二次剂量验证。结果:所有10例患者均成功通过SF2-ART流程重新规划,无需基于模拟的成像。整个计划和治疗过程,包括咨询、轮廓、自适应计划生成和QA,都在一次会议中完成。剂量学比较显示,无模拟适应性计划和临床交付计划之间的差异很小,所有病例的目标覆盖范围和正常组织约束都保持不变。中位总估计工作流程时间为166.4分钟。结论:这项计算机研究证明了使用当日自适应工作流在没有模拟CT的情况下提供空间分馏SBRT的可行性。SF2-ART方法可以为紧急或有症状的患者提供快速、高质量的治疗,并支持未来的前瞻性临床实施。
{"title":"In-Silico Trial of Same-Day Simulation-Free Spatially Fractionated Adaptive Radiotherapy (SF<sup>2</sup>-ART).","authors":"Dennis N Stanley, Alyssa R Birchmeier, Carlos E Cardenas, Richard A Popple, Natalie Viscariello, Joel A Pogue, Courtney B Stanley, Mehran Yusuf, Michael Soike, Samuel R Marcrom, Joseph Harms","doi":"10.1002/acm2.70517","DOIUrl":"https://doi.org/10.1002/acm2.70517","url":null,"abstract":"<p><strong>Purpose: </strong>Here we present an in-silico trial of the feasibility and deliverability of a same-day, simulation-free workflow for spatially fractionated adaptive radiotherapy (SF<sup>2</sup>-ART) using the Varian Ethos platform.</p><p><strong>Methods and materials: </strong>Ten patients (five thoracic and five extremity), previously treated with spatially fractionated radiotherapy (SFRT), were selected for this in silico trial. A two-phase regimen was simulated: Phase 1 delivered 12 Gy SBRT to a uniform, predefined high-dose lattice and 4 Gy to the gross tumor volume (GTV); Phase 2 consisted of 4 additional fractions of 4 Gy to the GTV. The planning workflow was performed entirely in silico, without the need for CT simulation. High-dose sphere matrices were generated with a custom script and aligned to physician-defined GTVs. Adaptive plans were created based on CBCT anatomy and evaluated for dosimetric quality, deliverability, and workflow timing. Comparisons were made to the original clinically delivered plans. Mobius3D was used for secondary dose verification.</p><p><strong>Results: </strong>All 10 cases were successfully replanned using the SF<sup>2</sup>-ART workflow without simulation-based imaging. The entire planning and treatment process, including consultation, contouring, adaptive plan generation, and QA, was performed within a single session. Dosimetric comparisons showed minimal differences between simulation-free adaptive and clinically delivered plans, with target coverage and normal tissue constraints maintained across all cases. Median total estimated workflow time was 166.4 min.</p><p><strong>Conclusions: </strong>This in-silico study demonstrates the feasibility of delivering spatially fractionated SBRT without simulation CT using a same-day adaptive workflow. The SF<sup>2</sup>-ART approach may enable rapid, high-quality treatment for patients with urgent or symptomatic presentations and supports future prospective clinical implementation.</p>","PeriodicalId":14989,"journal":{"name":"Journal of Applied Clinical Medical Physics","volume":"27 2","pages":"e70517"},"PeriodicalIF":2.2,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146207001","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Evaluating equivalent square field size definitions for rectangular small fields. 评估矩形小场的等效方形场大小定义。
IF 2.2 4区 医学 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2026-02-01 DOI: 10.1002/acm2.70500
Ignasi Méndez, Mateb Al Khalifa, Haya Aljuaid, Božidar Casar

Background: In the IAEA TRS-483 Code of Practice (CoP), rectangular small field sizes are approximated to equivalent square small fields using the definition proposed by Cranmer-Sargison et al. However, the CoP estimates the uncertainties associated with this formula only for rectangular fields with dimensions within the range 0.7 < X / Y < 1.4 $0.7 < X/Y < 1.4$ .

Purpose: The objective of the present study was to compare the accuracy of the Cranmer-Sargison definition with other formulas for equivalent square small fields in the context of measuring field output factors (FOFs) for rectangular small fields, both within and outside the range covered by the CoP.

Methods: Measurements were conducted using Gafchromic EBT4 radiochromic films. The models compared included Cranmer-Sargison, Sterling, Superellipse, Sterling-Partial Superellipse, Sterling-Superellipse, Vadash and Bjärngard, and Fogliata. The most accurate definition of equivalent square field size was identified as the one yielding the lowest discrepancy between measured and analytical values, with the log-likelihood of the measurements selected as the metric. Analytical values were derived using the function introduced by Sauer and Wilbert, which relates FOFs to equivalent square field sizes.

Results: The best results were achieved with the Fogliata model, followed in terms of accuracy by the Sterling-Partial Superellipse model. The Sterling-Superellipse and Vadash and Bjärngard models came next. It should be noted that the Sterling-Partial Superellipse and Sterling-Superellipse models rely solely on the geometric shape of the irradiation field size, whereas the Fogliata and Vadash and Bjärngard models incorporate a fitting parameter. The Sterling definition, while less accurate than these models, improved upon the Cranmer-Sargison definition and retained computational simplicity. Finally, the Cranmer-Sargison and Superellipse models exhibited the largest discrepancies.

Conclusions: This study identified several definitions of equivalent square small field size that could refine the IAEA TRS-483 CoP by improving the accuracy of field output correction factors for rectangular small fields. Among these definitions, the Fogliata model obtained the best results.

背景:在IAEA TRS-483操作规范(CoP)中,矩形小场尺寸使用Cranmer-Sargison等人提出的定义近似为等效方形小场。然而,CoP仅对尺寸在0.7 X/Y 1.4$ 0.7 < X/Y < 1.4$范围内的矩形场估算与该公式相关的不确定性。目的:本研究的目的是在测量矩形小场的场输出因子(fof)的背景下,比较Cranmer-Sargison定义与其他等效方形小场公式的准确性,包括在CoP覆盖范围内和之外。方法:采用Gafchromic EBT4放射线致变色薄膜进行测定。比较的模型包括Cranmer-Sargison、Sterling、Superellipse、Sterling- partial Superellipse、Sterling-Superellipse、Vadash和Bjärngard以及Fogliata。最准确的等效方场大小定义被确定为测量值和分析值之间产生最小差异的定义,并选择测量值的对数似然作为度量。利用Sauer和Wilbert引入的函数推导出解析值,该函数将fof与等效的平方场大小联系起来。结果:Fogliata模型的准确率最高,Sterling-Partial Superellipse模型次之。接下来是Sterling-Superellipse、Vadash和Bjärngard模型。值得注意的是,Sterling-Partial Superellipse和Sterling-Superellipse模型仅依赖于辐照场尺寸的几何形状,而Fogliata和Vadash以及Bjärngard模型则包含了一个拟合参数。斯特林定义虽然不如这些模型精确,但在克兰默-萨吉森定义的基础上进行了改进,并保持了计算的简单性。最后,Cranmer-Sargison模型和Superellipse模型表现出最大的差异。结论:本研究确定了几种等效方形小场尺寸的定义,通过提高矩形小场输出校正系数的精度,可以对IAEA TRS-483 CoP进行细化。在这些定义中,Fogliata模型获得了最好的结果。
{"title":"Evaluating equivalent square field size definitions for rectangular small fields.","authors":"Ignasi Méndez, Mateb Al Khalifa, Haya Aljuaid, Božidar Casar","doi":"10.1002/acm2.70500","DOIUrl":"10.1002/acm2.70500","url":null,"abstract":"<p><strong>Background: </strong>In the IAEA TRS-483 Code of Practice (CoP), rectangular small field sizes are approximated to equivalent square small fields using the definition proposed by Cranmer-Sargison et al. However, the CoP estimates the uncertainties associated with this formula only for rectangular fields with dimensions within the range <math> <semantics><mrow><mn>0.7</mn> <mo><</mo> <mi>X</mi> <mo>/</mo> <mi>Y</mi> <mo><</mo> <mn>1.4</mn></mrow> <annotation>$0.7 < X/Y < 1.4$</annotation></semantics> </math> .</p><p><strong>Purpose: </strong>The objective of the present study was to compare the accuracy of the Cranmer-Sargison definition with other formulas for equivalent square small fields in the context of measuring field output factors (FOFs) for rectangular small fields, both within and outside the range covered by the CoP.</p><p><strong>Methods: </strong>Measurements were conducted using Gafchromic EBT4 radiochromic films. The models compared included Cranmer-Sargison, Sterling, Superellipse, Sterling-Partial Superellipse, Sterling-Superellipse, Vadash and Bjärngard, and Fogliata. The most accurate definition of equivalent square field size was identified as the one yielding the lowest discrepancy between measured and analytical values, with the log-likelihood of the measurements selected as the metric. Analytical values were derived using the function introduced by Sauer and Wilbert, which relates FOFs to equivalent square field sizes.</p><p><strong>Results: </strong>The best results were achieved with the Fogliata model, followed in terms of accuracy by the Sterling-Partial Superellipse model. The Sterling-Superellipse and Vadash and Bjärngard models came next. It should be noted that the Sterling-Partial Superellipse and Sterling-Superellipse models rely solely on the geometric shape of the irradiation field size, whereas the Fogliata and Vadash and Bjärngard models incorporate a fitting parameter. The Sterling definition, while less accurate than these models, improved upon the Cranmer-Sargison definition and retained computational simplicity. Finally, the Cranmer-Sargison and Superellipse models exhibited the largest discrepancies.</p><p><strong>Conclusions: </strong>This study identified several definitions of equivalent square small field size that could refine the IAEA TRS-483 CoP by improving the accuracy of field output correction factors for rectangular small fields. Among these definitions, the Fogliata model obtained the best results.</p>","PeriodicalId":14989,"journal":{"name":"Journal of Applied Clinical Medical Physics","volume":"27 2","pages":"e70500"},"PeriodicalIF":2.2,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12887976/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146149427","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Evaluation and implementation of an independent Kilovoltage X-ray-based imaging platform for carbon ion radiotherapy. 碳离子放射治疗独立的Kilovoltage x射线成像平台的评估与实现。
IF 2.2 4区 医学 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2026-02-01 DOI: 10.1002/acm2.70501
Yixiao Guo, Zhiqiang Liu, Qingzhen Zhu, Ming Cai, Hongyi Cai, Ruifeng Liu, Qiuning Zhang, Zhiguo Xu

Background: Image-guided particle therapy (IGPT) has significantly advanced in recent years, particularly in the context of proton therapy. However, imaging solutions for carbon-ion radiotherapy (C-ion RT) remain limited.

Purpose: This study introduces sliding-gantry cone-beam computed tomography (CBCT) and dual-panel digital radiography (DR) systems, both mechanically independent of carbon-ion delivery nozzles. We aim to evaluate the image quality metrics and verify the positioning accuracy of the imaging systems.

Methods: Image quality was evaluated in terms of spatial resolution, low contrast resolution, image uniformity, and effective imaging area using a multi-purpose imaging phantom, Catphan 700 phantom, and ImageJ software. The influences of planning computed tomography (CT) slice thicknesses (1-5 mm), radiation quality settings (90-130 kV), and registration algorithms (bony, grayscale, and fiducial marker registrations) on positioning accuracy were assessed using anthropomorphic head-neck and thoracoabdominal phantom images. The clinical feasibility of both systems was validated in 22 enrolled patients.

Results: The CBCT exhibited a lower in-plane spatial resolution (2.50 line pairs per millimeter (lp/mm)) than DR (2.80 lp/mm). Spatial resolution of the CBCT system was measured at 0.90 lp/mm using the CTP 714 module of the Catphan 700 phantom. Both systems achieved a low contrast resolution of 2.30%. DR provided superior image uniformity (1.12%-1.40%) compared with CBCT (2.20%). The effective imaging areas were comparable between the CBCT and DR systems (99.30%-99.50%). Positioning accuracy varied with planning CT slice thicknesses, radiation quality settings, and registration algorithms, showing mean translation displacements ranging from 0.01 to 0.48 mm. CBCT achieved inter-fraction translational positioning errors within 2 mm in 42.3% (22/52) of fractions and rotational positioning errors within 2° in 80.8% (42/52) of fractions, and DR achieved 33.8% (24/71) and 73.2% (52/71), respectively.

Conclusion: The developed CBCT and DR systems achieved superior image quality and sub-0.5 mm positioning accuracy. These findings support the clinical feasibility of integrating CBCT and DR imaging systems into the C-ion RT workflow.

背景:近年来,图像引导粒子治疗(IGPT)取得了显著进展,特别是在质子治疗的背景下。然而,碳离子放疗(C-ion RT)的成像解决方案仍然有限。目的:本研究介绍了滑动龙门锥束计算机断层扫描(CBCT)和双面板数字射线成像(DR)系统,这两种系统在机械上都独立于碳离子输送喷嘴。我们的目的是评估图像质量指标和验证成像系统的定位精度。方法:采用多用途成像模体、Catphan 700模体和ImageJ软件,从空间分辨率、低对比度分辨率、图像均匀性和有效成像面积等方面评价图像质量。利用拟人头颈和胸腹影像评估规划计算机断层扫描(CT)层厚度(1-5 mm)、辐射质量设置(90-130 kV)和配准算法(骨、灰度和基准标记配准)对定位精度的影响。在22名入组患者中验证了两种系统的临床可行性。结果:CBCT的平面内空间分辨率(2.50线对/毫米(lp/mm))低于DR (2.80 lp/mm)。使用Catphan 700模体的CTP 714模块测量CBCT系统的空间分辨率为0.90 lp/mm。两种系统都实现了2.30%的低对比度分辨率。与CBCT(2.20%)相比,DR具有更好的图像均匀性(1.12% ~ 1.40%)。CBCT和DR系统的有效成像面积相当(99.30% ~ 99.50%)。定位精度随规划CT切片厚度、辐射质量设置和配准算法而变化,显示平均平移位移范围为0.01至0.48 mm。CBCT在42.3%(22/52)的分数间平移定位误差在2mm以内,在80.8%(42/52)的分数间旋转定位误差在2°以内,DR分别为33.8%(24/71)和73.2%(52/71)。结论:开发的CBCT和DR系统具有较好的图像质量和低于0.5 mm的定位精度。这些发现支持了将CBCT和DR成像系统整合到c离子RT工作流程中的临床可行性。
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引用次数: 0
Evaluation of the InTempo path set for CyberKnife prostate and lung SBRT: A single-institution experience. 对射波刀前列腺和肺部SBRT的InTempo路径的评估:单一机构的经验。
IF 2.2 4区 医学 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2026-02-01 DOI: 10.1002/acm2.70509
Yingcui Jia, Lei Fu, Shari Rudoler, Eric Gressen, Yevgeniy Vinogradskiy, Qianyi Xu
<p><strong>Purpose: </strong>The InTempo adaptive imaging system is an important component of the Accuray CyberKnife System, designed to enhance the system's ability to track and correct tumor motion during treatment. However, a limitation of this feature is the reduction of available nodes for treatment planning. The impact of a reduced number of nodes on the quality of InTempo-based treatment plans has not previously been evaluated. This retrospective study aims to compare the dosimetry of CyberKnife plans with and without The InTempo path set for both prostate and lung stereotactic body radiotherapy (SBRT).</p><p><strong>Methods: </strong>This study included twelve consecutive prostate SBRT patients and twenty selected lung SBRT patients. The selection criteria for the 20 lung patients were motivated by being able to construct a data set representative of common treatment tracking methods and dose prescriptions. To evaluate the impact of InTempo imaging, treatment plans were re-optimized using the same optimization parameters and machine settings, except for the path set with the maximum number of nodes. To ensure a fair comparison, the study plans were prescribed using identical planning target volume coverage as the clinical treatment plans. Statistical analyses were performed using mean and standard deviation, dose metric plots, and a two-sided Wilcoxon signed rank test with multiple testing correction to compare dose metrics between different path sets.</p><p><strong>Results: </strong>No statistically significant differences were observed among the Prostate, Prostate_Short, and their corresponding InTempo path sets in at least 8 of the 14 evaluated plan metrics, including prostate clinical tumor volume (CTV) V40Gy(%), conformity index, and homogeneity index. For example, the mean prostate CTV V40Gy (%) for the Prostate, Prostate_Short, and their corresponding InTempo path sets was 90.8 ± 4.7, 89.4 ± 4.7, 90.2 ± 3.9, 91.0 ± 7.0, respectively. However, compared with the Prostate path set, the Prostate_InTempo path set exhibited a statistically significant reduction in delivery time (p = 0.0010), number of beams, and bladder V18Gy (%), along with a statistically significant increase in the number of imaging beams (p = 0.0010). Additionally, Prostate_Short demonstrated statistically significant reductions in delivery time and number of beams compared with the Prostate path set, while the number of imaging beams remained statistically equivalent. In contrast, the Reduced_Prostate and Reduced_Prostate_InTempo sets consistently resulted in inferior dosimetric outcomes, with several plans deemed unoptimizable due to insufficient node availability. For lung SBRT, statistically significant differences were observed in delivery time and the number of imaging beams between plans with and without InTempo. However, no statistical differences were found in dose distribution metrics between these two lung groups.</p><p><strong>Conclusions: </strong>InTemp
目的:InTempo自适应成像系统是Accuray射波刀系统的重要组成部分,旨在增强系统在治疗过程中跟踪和纠正肿瘤运动的能力。然而,该特性的一个限制是减少了治疗计划的可用节点。减少淋巴结数量对以intempo为基础的治疗计划质量的影响以前没有被评估过。本回顾性研究旨在比较射波刀计划在前列腺和肺立体定向放射治疗(SBRT)中使用和不使用InTempo路径设置的剂量学。方法:本研究纳入12例连续的前列腺SBRT患者和20例选择的肺部SBRT患者。20例肺部患者的选择标准的动机是能够构建一个代表常用治疗跟踪方法和剂量处方的数据集。为了评估InTempo成像的影响,使用相同的优化参数和机器设置对治疗方案进行了重新优化,除了具有最大节点数的路径设置。为确保公平比较,研究计划与临床治疗计划采用相同的计划目标体积覆盖率。采用均数和标准差、剂量计量图和双侧Wilcoxon sign rank检验(多重检验校正)进行统计分析,比较不同路径集之间的剂量计量。结果:在14个评估的计划指标中,前列腺临床肿瘤体积(CTV) V40Gy(%)、符合性指数和均匀性指数等至少8个指标中,前列腺、Prostate_Short及其相应的InTempo路径组之间无统计学差异。例如,前列腺、Prostate_Short及其对应的InTempo路径集的平均前列腺CTV V40Gy(%)分别为90.8±4.7、89.4±4.7、90.2±3.9、91.0±7.0。然而,与前列腺路径组相比,Prostate_InTempo路径组在递送时间(p = 0.0010)、光束数和膀胱V18Gy(%)方面具有统计学意义的减少,同时在成像光束数方面具有统计学意义的增加(p = 0.0010)。此外,与前列腺路径设置相比,Prostate_Short显示在传送时间和光束数量上有统计学意义的减少,而成像光束数量在统计学上保持相等。相比之下,Reduced_Prostate和Reduced_Prostate_InTempo集合一致导致较差的剂量学结果,由于节点可用性不足,一些计划被认为是不可优化的。对于肺部SBRT,在使用和不使用InTempo的方案之间,在交付时间和成像光束数量上观察到统计学上的显著差异。然而,两组间剂量分布指标无统计学差异。结论:如果提供足够的淋巴结可用性,intempo兼容路径集不会显著影响前列腺或肺部SBRT的计划质量。具体来说,与前列腺路径组相比,Prostate_InTempo和Prostate_Short路径组显示了递送时间的减少和自适应成像频率的增加。然而,reduced_前列腺和Reduced_Prostate_InTempo会导致较差的计划质量和降低交付性,应谨慎使用。这些发现支持在不牺牲剂量学完整性的情况下选择性地使用InTempo成像进行SBRT计划。
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引用次数: 0
Dosimetric impact of port number in TomoDirect-based lower-body total body irradiation. 基于tomodirect的下体全身照射中端口号的剂量学影响。
IF 2.2 4区 医学 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2026-02-01 DOI: 10.1002/acm2.70504
Yoshiki Suetsugu, Naoki Higashi, Yukihide Fukuyama, Yuka Yamanaka, Keiki Inoue, Shun Nakano, Hiromi Terashima, Tomonari Sasaki

Background: The feasibility of total body irradiation (TBI) delivery using the TomoDirect mode of a TomoTherapy system has been demonstrated. In clinical practice, TomoTherapy-based TBI is typically performed in two parts: upper and lower body.

Purpose: This study aimed to evaluate the dosimetric impact of varying port numbers on dose evaluation indices for lower body irradiation using TomoDirect and to compare these results with those of TomoHelical in a simulation setting.

Methods: Sixteen patients who underwent myeloablative TBI using TomoHelical between October 2017 and March 2021 were retrospectively analyzed. TomoDirect plans with 2 to 12 ports at approximately equal beam angles were generated (modulation factor = 1.5, field width = 5.0 cm, pitch = 0.500). TomoHelical plans used identical parameters except for a pitch of 0.397. The prescribed dose was 12 Gy in six fractions. Dose indices (D2, D98, D50, homogeneity index [HI]) and beam-on time were compared.

Results: In TomoDirect plans, all dose evaluation indices worsened as the number of ports increased up to five, but changes became minimal beyond eight ports. D2 was significantly improved in all TomoDirect plans compared with those of TomoHelical plan. D98 was significantly lower for the three- and five-port TomoDirect plans, and no TomoDirect plan achieved higher D98 than TomoHelical. The D50 and HI were significantly improved in all TomoDirect plans except the five-port configuration. The two-port TomoDirect plan achieved the most favorable dose indices and the shortest beam-on time.

Conclusions: The two-port TomoDirect approach with anterior-posterior beam configuration provides an efficient and clinically reasonable option for lower-body irradiation, offering improved dose homogeneity and reduced treatment time compared with TomoHelical.

背景:使用TomoDirect模式的TomoTherapy系统的全身照射(TBI)递送的可行性已经被证明。在临床实践中,基于断层治疗的TBI通常在两个部分进行:上半身和下半身。目的:本研究旨在评估不同端口号对使用TomoDirect进行下体照射剂量评估指标的剂量学影响,并在模拟环境下将这些结果与TomoHelical的结果进行比较。方法:回顾性分析2017年10月至2021年3月期间使用TomoHelical进行清髓性TBI手术的16例患者。生成2 ~ 12个端口的TomoDirect图,波束角大致相等(调制因子= 1.5,场宽= 5.0 cm,节距= 0.500)。TomoHelical计划使用相同的参数,除了间距为0.397。处方剂量为12戈瑞,分6份服用。比较剂量指数(D2、D98、D50、均匀性指数[HI])和照射时间。结果:在TomoDirect计划中,当端口数增加到5个时,所有剂量评价指标都恶化,但超过8个端口变化最小。与TomoDirect计划相比,所有TomoDirect计划的D2均显著提高。三端口和五端口TomoDirect计划的D98明显低于TomoDirect计划,没有TomoDirect计划的D98高于TomoHelical。除五端口配置外,所有TomoDirect计划的D50和HI都有显着改善。双端口TomoDirect计划获得了最有利的剂量指数和最短的光束照射时间。结论:与TomoHelical相比,采用前后光束配置的双端口TomoDirect入路为下体照射提供了一种有效且临床上合理的选择,可改善剂量均匀性并缩短治疗时间。
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引用次数: 0
Evaluation of QUASAR Insight Phantom for daily imaging QA of MRgRT linacs. QUASAR Insight Phantom对MRgRT直线机日常成像质量的评价。
IF 2.2 4区 医学 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2026-02-01 DOI: 10.1002/acm2.70463
Eli Grant, Jiayi Liu, Ronak Etemadpour, Chengyu Shi, Huisi Ai, Percy Lee, Terence Williams, An Liu, Borna Maraghechi

Purpose: Magnetic resonance imaging (MRI) and its importance in modern radiation therapy requires a standardized daily quality assurance (QA) procedure that is both comprehensive and efficient. Current imaging QA guidelines require a more inclusive analysis of imaging characteristics, as well as a simplification of setup procedures. We have studied the feasibility of using the Insight Phantom to provide consistent images for analyses of uniformity, slice thickness, spatial resolution, and distortion across a large field of view (FOV).

Methods: The large imaging region of the Insight Phantom was imaged using 3D True Fast Imaging with Steady State Precession (TruFi) and analyzed using the Modus QA software. The base and upright section were imaged in coronal, axial, and sagittal orientations over 3 months.

Results: Geometric distortion analysis yielded average maximum distortions within a 210 mm diameter of 0.57, 0.73, and 0.45 mm for axial, sagittal, and coronal orientations, respectively. Similarly, within a 310 mm diameter, average maximum distortions were 0.58, 0.73, and 0.74 mm with no distortions greater than or equal to 1 mm. Average modulation transfer function (MTF) values were 0.431 ± 0.007, 0.436 ± 0.007, and 0.433 ± 0.010 lp/mm for axial, sagittal, and coronal images, respectively. Finally, slice thickness values were consistent at 2.19 ± 0.04, 2.22 ± 0.06, and 2.24 ± 0.07 mm for axial, sagittal, and coronal imaging orientations, respectively. Images were repeatable and setup procedures were quick and straightforward, enhancing therapist workflow and efficiency.

Conclusion: The Insight Phantom's large coverage allows a more in-depth analysis of the MRI's large FOV, and its simple setup ensures a repeatable daily QA procedure for therapists. The software also provides a comprehensive analysis of key imaging parameters in a detailed report that can be used to monitor MRI functionality and quality.

目的:磁共振成像(MRI)及其在现代放射治疗中的重要性需要一个标准化的日常质量保证(QA)程序,该程序既全面又高效。当前的成像QA指南要求对成像特征进行更全面的分析,并简化设置程序。我们已经研究了使用Insight Phantom为分析均匀性、切片厚度、空间分辨率和大视场(FOV)失真提供一致图像的可行性。方法:采用稳态进动3D真快速成像技术(TruFi)对Insight Phantom的大成像区域进行成像,并用Modus QA软件进行分析。在3个月的时间里,在冠状、轴状和矢状方向上对基底和直立切片进行成像。结果:几何畸变分析显示,210 mm直径内的轴向、矢状和冠状方向的平均最大畸变分别为0.57、0.73和0.45 mm。同样,在310毫米直径内,平均最大畸变为0.58、0.73和0.74毫米,没有畸变大于或等于1毫米。轴位、矢状位和冠状位的平均调制传递函数(MTF)分别为0.431±0.007、0.436±0.007和0.433±0.010 lp/mm。最后,轴位、矢状位和冠状位的切片厚度值分别为2.19±0.04、2.22±0.06和2.24±0.07 mm。图像可重复,设置程序快速直接,提高了治疗师的工作流程和效率。结论:Insight Phantom的大覆盖范围允许对MRI的大视场进行更深入的分析,其简单的设置确保了治疗师可重复的日常QA程序。该软件还在详细报告中提供了关键成像参数的全面分析,可用于监测MRI功能和质量。
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引用次数: 0
The geometric accuracy of off-axis targets in stereotactic body radiotherapy treatments across three linear accelerators. 立体定向体放射治疗中三线加速器离轴靶的几何精度。
IF 2.2 4区 医学 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2026-02-01 DOI: 10.1002/acm2.70383
Dinesan Chinnaiya, Gopinath Mudhana

Purpose: This study quantifies isocenter and off-axis geometric uncertainties using MultiMet Winston-Lutz (WL) tests to optimize gross tumour volume (GTV)-to-PTV (planning target volume) margin for single isocenter multiple target (SIMT) stereotactic body radiotherapy (SBRT) across three linear accelerators.

Methods and materials: Geometric inaccuracies were quantified for Trilogy (HD-MLC, 6 MV SRS), TrueBeam (Millennium MLC), and TrueBeam STx (HD-MLC, 6-degrees-of-freedom (6DoF) couch) using a Sun Nuclear MultiMet-WL cube containing six tungsten carbide markers arranged along the superior-inferior axis. The electronic portal imaging device (EPID) images acquired at four cardinal gantry angles with varied collimator/couch rotations were analyzed using MultiMet-WL software (v2.1) to measure 3D (Δ) displacements for all the LINACs. The required GTV-to-PTV margins were calculated using a modified van Herk formula (2.5Σ+1.64σ), incorporating measured 3D displacements for isocenter and off-axis targets.

Results: The TrueBeam STx (HD-MLC/6DoF) demonstrated superior geometric accuracy, maintaining ≤0.5 mm isocenter precision and ≤0.59 mm off-axis targeting (3-7 cm). The Trilogy exceeded TG-142 tolerances (1.06 ± 0.59 to 1.09 ± 0.57 mm) at all targets, requiring 4 mm uniform margins, while the TrueBeam (MMLC) showed optimal variations (isocenter: 0.68 ± 0.34 mm; superior off-axis: 0.74 ± 0.36 mm). Both TrueBeam platforms achieved sub-millimeter accuracy but demonstrated direction dependency for off-axis targets, requiring 2-3 mm anisotropic margins. Notably, isotropic margins introduced up to 11% delineation errors for off-axis targets due to these machine-specific geometric variations, highlighting the imperative for platform-specific margin protocols in SIMT SBRT.

Conclusion: This study demonstrates that routine analysis of MultiMet WL testing is an essential tool for the spatial accuracy of the LINAC to establish machine-specific PTV margin expansion in SIMT-SBRT, particularly for targets where rotational errors dominate.

目的:本研究使用MultiMet Winston-Lutz (WL)测试量化等中心和离轴几何不确定性,以优化单等中心多靶点(SIMT)立体定向体放疗(SBRT)的总肿瘤体积(GTV)- ptv(计划靶体积)裕度。方法和材料:使用Sun Nuclear multimett - wl立方体,包含沿上-下轴排列的六个碳化钨标记物,对Trilogy (HD-MLC, 6 MV SRS)、TrueBeam (Millennium MLC)和TrueBeam STx (HD-MLC, 6自由度沙发)的几何不准确性进行量化。使用MultiMet-WL软件(v2.1)分析在四个基本龙门角度获得的电子门户成像设备(EPID)图像,以测量所有LINACs的3D (Δ)位移。采用改进的van Herk公式(2.5Σ+1.64σ)计算所需的gtv - ptv余量,并结合测量的等心和离轴目标的三维位移。结果:TrueBeam STx (HD-MLC/6DoF)具有优异的几何精度,可保持≤0.5 mm的等心精度和≤0.59 mm的离轴瞄准(3-7 cm)。Trilogy在所有目标上都超过TG-142公差(1.06±0.59至1.09±0.57 mm),要求4 mm的均匀裕度,而TrueBeam (MMLC)表现出最佳的变化(等心:0.68±0.34 mm,离轴:0.74±0.36 mm)。这两个TrueBeam平台都实现了亚毫米精度,但在离轴目标上表现出方向依赖性,需要2-3毫米的各向异性边缘。值得注意的是,由于这些特定于机器的几何变化,各向同性边界为离轴目标引入了高达11%的描述误差,突出了SIMT SBRT中特定于平台的边界协议的必要性。结论:本研究表明,MultiMet WL测试的常规分析是LINAC空间精度的重要工具,可以在SIMT-SBRT中建立特定机器的PTV裕度扩展,特别是对于旋转误差占主导地位的目标。
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Journal of Applied Clinical Medical Physics
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