In vivo transit dosimetry methodology for whole breast intensity modulated radiation therapy.

IF 2 4区 医学 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Lucia Zirone, Elisa Bonanno, Giuseppina R Borzì, Nina Cavalli, Alessia D'Anna, Andrea Girlando, Martina Pace, Giuseppe Stella, Carmelo Marino
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Abstract

Background: In vivo transit dosimetry using an electronic portal imaging device (EPID-IVTD) is an important tool for verifying the accuracy of radiation therapy treatments. Despite its potential, the implementation of EPID-IVTD in breast intensity modulated radiation therapy (IMRT) treatments has not yet been standardized, limiting its clinical adoption. A standardized EPID-IVTD method could enhance treatment accuracy and improve patient safety in routine clinical practice.

Purpose: This study aims to develop a method for EPID-IVTD for whole breast IMRT treatment.

Methods: Gamma passing rates (GPRs) analysis was the basis of the work conducted on a dataset of 50 patients. The first phase of the work focused on the identification of the reference fraction. In the second phase a method for performing EPID-IVTD was implemented. Lower-tolerance and -action limits (l-TL and l-AL), as introduced by AAPM TG 218, were employed to determine the reference fraction and used as alert and alarm thresholds, respectively, in EPID-IVTD monitoring.

Results: The first treatment fraction demonstrated the best dosimetric agreement with the theoretical plan and was therefore used as the reference in the second phase of the study. EPID-IVTD results showed that 75% of the GPRs ranged from 97.5% to 99.9%, 93.83% were above the l-TL, 4.31% fell between l-TL and l-AL, and 1.86% were below l-AL.

Conclusions: A method for the implementation of an effective EPID-IVTD in whole breast IMRT treatment was developed and is now routinely applied at our center, enabling efficient monitoring in clinical practice.

全乳强度调制放射治疗的体内传输剂量法。
背景:使用电子门静脉成像装置(EPID-IVTD)进行体内传输剂量测定是验证放射治疗准确性的重要工具。尽管具有潜力,EPID-IVTD在乳房强度调节放疗(IMRT)治疗中的实施尚未标准化,限制了其临床应用。标准化的EPID-IVTD方法可以提高常规临床治疗的准确性,提高患者的安全性。目的:研究EPID-IVTD在全乳IMRT治疗中的应用。方法:Gamma通过率(GPRs)分析是对50例患者数据集进行工作的基础。第一阶段的工作重点是鉴定参考分数。在第二阶段,实现了执行EPID-IVTD的方法。采用AAPM TG 218引入的低耐受限值和低作用限值(l-TL和l-AL)来确定参考分数,并分别作为EPID-IVTD监测的警报和报警阈值。结果:第一个处理分数与理论计划的剂量学一致性最好,因此被用作第二阶段研究的参考。EPID-IVTD结果显示,75%的gpr在97.5% ~ 99.9%之间,93.83%的gpr高于l-TL, 4.31%介于l-TL和l-AL之间,1.86%低于l-AL。结论:我们开发了一种在全乳IMRT治疗中实施EPID-IVTD的有效方法,目前已在我中心常规应用,可在临床实践中进行有效的监测。
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来源期刊
CiteScore
3.60
自引率
19.00%
发文量
331
审稿时长
3 months
期刊介绍: Journal of Applied Clinical Medical Physics is an international Open Access publication dedicated to clinical medical physics. JACMP welcomes original contributions dealing with all aspects of medical physics from scientists working in the clinical medical physics around the world. JACMP accepts only online submission. JACMP will publish: -Original Contributions: Peer-reviewed, investigations that represent new and significant contributions to the field. Recommended word count: up to 7500. -Review Articles: Reviews of major areas or sub-areas in the field of clinical medical physics. These articles may be of any length and are peer reviewed. -Technical Notes: These should be no longer than 3000 words, including key references. -Letters to the Editor: Comments on papers published in JACMP or on any other matters of interest to clinical medical physics. These should not be more than 1250 (including the literature) and their publication is only based on the decision of the editor, who occasionally asks experts on the merit of the contents. -Book Reviews: The editorial office solicits Book Reviews. -Announcements of Forthcoming Meetings: The Editor may provide notice of forthcoming meetings, course offerings, and other events relevant to clinical medical physics. -Parallel Opposed Editorial: We welcome topics relevant to clinical practice and medical physics profession. The contents can be controversial debate or opposed aspects of an issue. One author argues for the position and the other against. Each side of the debate contains an opening statement up to 800 words, followed by a rebuttal up to 500 words. Readers interested in participating in this series should contact the moderator with a proposed title and a short description of the topic
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