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妇科近距离治疗的体内剂量测定:物理和临床考量

In-vivo dosimetry for gynaecological brachytherapy: physical and clinical considerations.

作者信息

Waldhäusl Claudia, Wambersie André, Pötter Richard, Georg Dietmar

机构信息

Department of Radiotherapy and Radiobiology, University of Vienna, Vienna, Austria.

出版信息

Radiother Oncol. 2005 Dec;77(3):310-7. doi: 10.1016/j.radonc.2005.09.004. Epub 2005 Oct 14.

Abstract

INTRODUCTION

The study aimed to estimate the dosimetric uncertainty using diodes (PTW/Germany) for a high-dose rate Iridum-192 source under clinical conditions. Finally, the role of in-vivo dosimetry for cervix cancer patients was evaluated.

MATERIAL AND METHODS

First, diode calibration and factors influencing diode response were investigated and phantom studies compared doses measured and computed by the treatment planning system. Based on that, the uncertainty for diode measurements was estimated to be 7% (1 sigma). Secondly, 55 applications of patients with cervix carcinoma were evaluated. Doses in rectum and bladder were measured and compared to the computed doses and differences were calculated. If the differences exceeded 10% the corresponding shift in probe position was evaluated. Additionally, the in-vivo dosimetry data were compared to doses at the ICRU 38 [ICRU Report No. 38, dose and volume specification for reporting intracavitary therapy in gynaecology. In: Chassagne D, Dutreix A, Almond P, Burgers J, Busch M, Joslin C editors. International commissioning on radiation units and measurements. Bethesda: 1985.] reference points for rectum and bladder.

RESULTS

In patients, in-vivo dosimetry resulted in differences between calculated and measured doses ranging from -31 to+90% (mean 11%) for the rectum and from -27 to+26% (mean 4%) for the bladder. Shifts in probe position of 2.5mm for the rectal probe and 3.5mm for the bladder probe caused dose differences exceeding 10%. The dose at the ICRU rectum reference point was underestimated by the calculated doses at probe position ranging from -61 to 156% (mean 29%). The dose to the ICRU bladder reference point was underestimated by the calculated dose ranging from 12 to 162% (mean 58%).

CONCLUSION

The study shows that diode accuracy and reproducibility is sufficient for clinical applications. For accurate in-vivo dosimetry geometric conditions are of utmost importance. It is recommended that in-vivo dosimetry should be performed in addition to computation.

摘要

引言

本研究旨在评估在临床条件下使用二极管(德国PTW公司)对高剂量率铱 - 192源进行剂量测定的不确定性。最后,评估了体内剂量测定法对宫颈癌患者的作用。

材料与方法

首先,研究了二极管校准及影响二极管响应的因素,并通过模体研究比较了治疗计划系统测量和计算的剂量。在此基础上,估计二极管测量的不确定性为7%(1σ)。其次,评估了55例宫颈癌患者的应用情况。测量直肠和膀胱的剂量,并与计算剂量进行比较,计算差异。如果差异超过10%,则评估探头位置的相应偏移。此外,将体内剂量测定数据与国际辐射单位与测量委员会第38号报告(ICRU Report No. 38,妇科腔内治疗剂量和体积规范。Chassagne D、Dutreix A、Almond P、Burgers J、Busch M、Joslin C编辑。国际辐射单位与测量委员会。贝塞斯达:1985年)中直肠和膀胱参考点的剂量进行比较。

结果

在患者中,体内剂量测定结果显示,直肠计算剂量与测量剂量之间的差异为 - 31%至 + 90%(平均11%),膀胱为 - 27%至 + 26%(平均4%)。直肠探头位置偏移2.5mm和膀胱探头位置偏移3.5mm会导致剂量差异超过10%。在探头位置,计算剂量低估了ICRU直肠参考点剂量的 - 61%至156%(平均29%)。计算剂量低估了ICRU膀胱参考点剂量的12%至162%(平均58%)。

结论

该研究表明二极管的准确性和可重复性足以满足临床应用。对于准确的体内剂量测定,几何条件至关重要。建议除计算外还应进行体内剂量测定。

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