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比较三种不同计划流程下高剂量率阴道近距离放射治疗中危及器官的剂量。

Comparing organ-at-risk doses for high-dose-rate vaginal brachytherapy between three different planning workflows.

作者信息

Gruhl J D, Zheng D, Longo J L, Enke C, Wahl A O

机构信息

Department of Radiation Oncology, University of Nebraska Medical Center, Omaha, NE.

Department of Radiation Oncology, Medical College of Wisconsin, Milwaukee, WI.

出版信息

Brachytherapy. 2017 Mar-Apr;16(2):373-377. doi: 10.1016/j.brachy.2016.11.008. Epub 2016 Dec 28.

DOI:10.1016/j.brachy.2016.11.008
PMID:28039010
Abstract

PURPOSE

The aim of this study was to compare the organ-at-risk doses to the rectum and the bladder in postoperative endometrial cancer patients who receive high-dose-rate vaginal brachytherapy (HDR-VB), when using three different methods of treatment planning: (Workflow A) individualized treatment planning before every fraction, (Workflow B) individualized treatment planning for first fraction only), and (Workflow C) using a template plan based on applicator choice and prescription specifics without patient-specific imaging or planning (standardized template approach).

METHODS AND MATERIALS

Alternative plans were retrospectively created using workflows B and C for 22 patients who previously received postoperative HDR-VB using a vaginal cylinder and planned using Workflow A for endometrial cancer. The rectum and bladder were contoured on the CTs used for each fraction for dose comparison between the three methods. D, D, D, D, and V of the bladder and the rectum were compared using the two-sided Wilcoxon signed-rank test.

RESULTS

A total of 123 fractions were available for comparison. For Workflow A vs. Workflow B, there was no significant difference for any rectal or bladder dosimetric parameter. For Workflow A vs. Workflow C, Workflow A delivered a significantly higher median dose to the rectum than Workflow C for D, D, D, and V. Workflow C delivered a significantly higher dose to the bladder than Workflow A: D, D, D, and V. However, the magnitudes of the differences were small; the dose index difference was >75 cGy for only two fractions.

CONCLUSION

Plan standardization in HDR-VB may result in considerable time and cost savings with minimal organ-at-risk dose differences.

摘要

目的

本研究的目的是比较接受高剂量率阴道近距离放射治疗(HDR-VB)的子宫内膜癌术后患者,在使用三种不同治疗计划方法时,直肠和膀胱的危及器官剂量:(工作流程A)每次分割前进行个体化治疗计划,(工作流程B)仅对第一分割进行个体化治疗计划,以及(工作流程C)使用基于施源器选择和处方细节的模板计划,无需患者特异性成像或计划(标准化模板方法)。

方法和材料

对22例先前使用阴道柱状施源器接受术后HDR-VB并采用工作流程A进行子宫内膜癌计划的患者,回顾性地使用工作流程B和C创建替代计划。在用于各分割的CT上勾勒出直肠和膀胱,以比较三种方法之间的剂量。使用双侧Wilcoxon符号秩检验比较膀胱和直肠的D、D、D、D和V。

结果

共有123个分割可用于比较。对于工作流程A与工作流程B,任何直肠或膀胱剂量学参数均无显著差异。对于工作流程A与工作流程C,在D、D、D和V方面,工作流程A给予直肠的中位剂量显著高于工作流程C。工作流程C给予膀胱的剂量显著高于工作流程A:D、D、D和V。然而,差异幅度较小;仅两个分割的剂量指数差异>75 cGy。

结论

HDR-VB中的计划标准化可能会节省大量时间和成本,同时危及器官剂量差异最小。

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