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立体定向体部放射治疗中剂量适形性的多中心评估。

Multi-center evaluation of dose conformity in stereotactic body radiotherapy.

作者信息

Lee Jonny, Dean Christopher, Patel Rushil, Webster Gareth, Eaton David J

机构信息

National Radiotherapy Trials QA Group, Mount Vernon Hospital, London HA6 2RN, UK.

Barts Health NHS Trust, London EC1A 7BE, UK.

出版信息

Phys Imaging Radiat Oncol. 2019 Aug 28;11:41-46. doi: 10.1016/j.phro.2019.08.002. eCollection 2019 Jul.

Abstract

BACKGROUND AND PURPOSE

Stereotactic body radiotherapy (SBRT) is an emerging technique for treating oligometastases, but limited data is available on what plan quality is achievable for a range of modalities and clinical sites.

METHODS

SBRT plans for lung, spine, bone, adrenal, liver and node sites from 17 participating centers were reviewed. Centers used various delivery techniques including static and rotational intensity-modulation and multiple non-coplanar beams. Plans were split into lung and other body sites and evaluated with different plan quality metrics, including two which are independent of target coverage; "prescription dose spillage" (PDS) and "modified gradient index" (MGI). These were compared to constraints from the ROSEL and RTOG 0813 clinical trials.

RESULTS

Planning target volume (PTV) coverage was compromised (PTV V100% < 90%) in 29% of patient plans in order to meet organ-at-risk (OAR) tolerances, supporting the use of plan quality metrics which are independent of target coverage. Both lung (n = 48) and other body (n = 99) site PDS values agreed well with ROSEL constraints on dose spillage, but RTOG 0813 values were too high to detect sub-optimal plans. MGI values for lung plans were mis-matched to both sets of previous constraints, with ROSEL values too high and RTOG 0813 values too low. MGI values were lower for other body plans as expected, though this was only statistically significant for PTV volumes <20 cm.

CONCLUSIONS

Updated guidance for lung and other body site SBRT plan quality using the PDS and MGI metrics is presented.

摘要

背景与目的

立体定向体部放疗(SBRT)是一种治疗寡转移瘤的新兴技术,但关于一系列治疗方式和临床部位可实现的计划质量的数据有限。

方法

回顾了来自17个参与中心的肺、脊柱、骨、肾上腺、肝脏和淋巴结部位的SBRT计划。各中心采用了多种放疗技术,包括静态和旋转调强放疗以及多个非共面射束。计划被分为肺部和其他身体部位,并使用不同的计划质量指标进行评估,包括两个与靶区覆盖无关的指标:“处方剂量溢出”(PDS)和“修正梯度指数”(MGI)。将这些指标与ROSEL和RTOG 0813临床试验的限制条件进行比较。

结果

为了满足危及器官(OAR)的耐受度标准,29%的患者计划中计划靶体积(PTV)覆盖不足(PTV V100%<90%),这支持使用与靶区覆盖无关的计划质量指标。肺部(n = 48)和其他身体部位(n = 99)的PDS值均与ROSEL关于剂量溢出的限制条件相符,但RTOG 0813的值过高,无法检测出次优计划。肺部计划的MGI值与之前两组限制条件均不匹配,ROSEL的值过高,而RTOG 0813的值过低。正如预期的那样,其他身体部位计划的MGI值较低,不过仅在PTV体积<20 cm时具有统计学意义。

结论

给出了使用PDS和MGI指标对肺部和其他身体部位SBRT计划质量的更新指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1897/7807546/69c10c8393b4/gr1.jpg

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