SBRT/SRS patient-specific QA using GAFchromicTM EBT3 and FilmQATM Pro software.

IF 0.7 Q4 SURGERY Journal of radiosurgery and SBRT Pub Date : 2022-01-01
Giuseppe Stella, Nina Cavalli, Elisa Bonanno, Lucia Zirone, Giuseppina Rita Borzì, Martina Pace, Andrea Girlando, Anna M Gueli, Carmelo Marino
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Abstract

The aim of this work is to verify the potential use of GAFchromicTM EBT3 and FILMQATM pro software for patient specific quality assurance (QA) for stereotactic radiosurgery (SRS) and stereotactic body radiotherapy (SBRT) treatment plans in clinical routine use. In particular, encephalic, pulmonary and lymph node treatments plans were selected for this study. The agreement between the calculated and measured dose distributions were evaluated in terms of ɣ index with 3%3mm, 2%2mm, 1.5%1.5mm and 3%1.5mm criteria. The obtained results were then compared to the routine pre-treatment verification method which uses electronic portal imaging device (EPID) and EPIQA analysis software. EBT3-FilmQA method results show a mean ɣ index passing rate >95% with 2%1.5mm analysis criteria and an improvement of about 7% compared with EPID-EPIQA method results.

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使用GAFchromicTM EBT3和FilmQATM Pro软件进行SBRT/SRS患者特异性QA。
这项工作的目的是验证GAFchromicTM EBT3和FILMQATM pro软件在临床常规使用的立体定向放射外科(SRS)和立体定向放射治疗(SBRT)治疗计划中患者特定质量保证(QA)的潜在用途。本研究特别选择了脑、肺和淋巴结的治疗方案。以3%3mm、2%2mm、1.5%1.5mm和3%1.5mm为标准,用指数来评价计算剂量分布与测量剂量分布的一致性。然后将所得结果与常规的预处理验证方法进行比较,该方法采用电子门静脉成像装置(EPID)和EPIQA分析软件。EBT3-FilmQA方法在2%的1.5mm分析标准下,平均指标合格率>95%,较EPID-EPIQA方法提高约7%。
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CiteScore
1.40
自引率
8.30%
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