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在进行中的 EORTC 22042-26042 非典型性和恶性脑膜瘤试验中对放射治疗进行质量保证:模拟运行和前瞻性个别病例审查的结果。

Quality assurance of radiotherapy in the ongoing EORTC 22042-26042 trial for atypical and malignant meningioma: results from the dummy runs and prospective individual case Reviews.

机构信息

Department of Radiation Oncology, Ankara Oncology Hospital, Ankara, Turkey.

出版信息

Radiat Oncol. 2013 Jan 30;8:23. doi: 10.1186/1748-717X-8-23.

Abstract

BACKGROUND

The ongoing EORTC 22042-26042 trial evaluates the efficacy of high-dose radiotherapy (RT) in atypical/malignant meningioma. The results of the Dummy Run (DR) and prospective Individual Case Review (ICR) were analyzed in this Quality Assurance (QA) study.

MATERIAL/METHODS: Institutions were requested to submit a protocol compliant treatment plan for the DR and ICR, respectively. DR-plans (n=12) and ICR-plans (n=50) were uploaded to the Image-Guided Therapy QA Center of Advanced Technology Consortium server (http://atc.wustl.edu/) and were assessed prospectively.

RESULTS

Major deviations were observed in 25% (n=3) of DR-plans while no minor deviations were observed. Major and minor deviations were observed in 22% (n=11) and 10% (n=5) of the ICR-plans, respectively. Eighteen% of ICRs could not be analyzed prospectively, as a result of corrupted or late data submission. CTV to PTV margins were respected in all cases. Deviations were negatively associated with the number of submitted cases per institution (p=0.0013), with a cutoff of 5 patients per institutions. No association (p=0.12) was observed between DR and ICR results, suggesting that DR's results did not predict for an improved QA process in accrued brain tumor patients.

CONCLUSIONS

A substantial number of protocol deviations were observed in this prospective QA study. The number of cases accrued per institution was a significant determinant for protocol deviation. These data suggest that successful DR is not a guarantee for protocol compliance for accrued patients. Prospective ICRs should be performed to prevent protocol deviations.

摘要

背景

正在进行的 EORTC 22042-26042 试验评估了高剂量放疗(RT)在非典型/恶性脑膜瘤中的疗效。本质量保证(QA)研究分析了模拟运行(DR)和前瞻性个别病例审查(ICR)的结果。

材料/方法:要求各机构分别提交 DR 和 ICR 的符合方案的治疗计划。DR 计划(n=12)和 ICR 计划(n=50)被上传到先进技术联盟的图像引导治疗 QA 中心服务器(http://atc.wustl.edu/)并进行前瞻性评估。

结果

在 DR 计划中观察到 25%(n=3)存在主要偏差,而没有观察到次要偏差。在 ICR 计划中,分别观察到 22%(n=11)和 10%(n=5)的主要和次要偏差。由于数据提交延迟或损坏,18%的 ICR 无法进行前瞻性分析。所有情况下 CTV 到 PTV 的边缘均得到尊重。偏差与每个机构提交的病例数量呈负相关(p=0.0013),机构提交的病例数为 5 例。DR 和 ICR 结果之间未观察到关联(p=0.12),表明 DR 的结果不能预测累积脑肿瘤患者 QA 过程的改善。

结论

在这项前瞻性 QA 研究中观察到大量方案偏差。每个机构积累的病例数是方案偏差的一个重要决定因素。这些数据表明,成功的 DR 并不能保证对累积患者的方案遵守。应进行前瞻性 ICR 以防止方案偏差。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40e1/3564920/30da3ca455ab/1748-717X-8-23-1.jpg

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