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放射肿瘤学中的质量保证。一项关于乳腺癌放疗期间体内剂量测定计划的可行性及其对行动水平影响的研究。

Quality assurance in radiation oncology. A study of feasibility and impact on action levels of an in vivo dosimetry program during breast cancer irradiation.

作者信息

Cozzi L, Fogliata-Cozzi A

机构信息

Department of Radiation Oncology, Ospedale San Giovanni, Bellinzona, Switzerland.

出版信息

Radiother Oncol. 1998 Apr;47(1):29-36. doi: 10.1016/s0167-8140(97)00202-8.

Abstract

BACKGROUND AND PURPOSE

The study was aimed at investigating the feasibility and accuracy of an in vivo quality assurance program in radiotherapy. Breast irradiation was found to be a relevant clinical model due to the fairly good uniformity of the irradiated tissue.

MATERIALS AND METHODS

The investigation was based on an extension of the method described by Leunens et al. (Leunens, G., van Dam, J., Dutreix, A. and van der Schueren, E. Quality assurance in radiotherapy by in vivo dosimetry. 1. Entrance dose measurements, a reliable procedure. Radiother. Oncol. 17: 141-151, 1990; Leunens, G., van Dam, J., Dutreix, A. and van der Schueren, E. Quality assurance in radiotherapy by in vivo dosimetry. 2. Determination of the target absorbed dose. Radiother. Oncol. 19: 73-87, 1990; van Dam, J. and Marinello, G. Methods for in vivo dosimetry in external radiotherapy. Physics for clinical radiotherapy. ESTRO Booklet n. 1 (Garant), 1994), determining the absorbed dose at any point on the central axis from a measurement of entrance and exit doses with individually calibrated and corrected diodes. Treatment accuracy (delta) was quantified as the ratio of the measured and the expected isocentre dose from the treatment planning system (TPS).

RESULTS

A preliminary study was carried out on a Plexiglas slab phantom to test the method ending with a frequency distribution of delta with a mean of 0.04 +/- 0.05% and a standard deviation (SD) of 0.83 +/- 0.04%. In the in vivo study, 101 patients irradiated with two tangential fields were included in the protocol over a 1-year period. The total number of patient set-ups analyzed was 421 giving a distribution of delta with a mean of -1.3 +/- 0.2% and an SD of 2.7 +/- 0.1% without any correction. Taking into account temperature effects and set-up errors as SSD accuracy and diodes positioning it was possible to implement an off-line correction method leading to a final distribution with a mean of -1.9 +/- 0.2% and an SD of 2.4 +/- 0.1%. Individual cases with large deviations were detected and evaluated and actions were undertaken whenever possible.

CONCLUSIONS

The study showed that diodes can be easily used by radiographers in an accurate in vivo quality assurance (QA) program and that an accuracy level of 3% at 1 SD can be reached on average. Attention and action levels can also be identified and careful evaluation of positioning and morphological variations during treatment should be part of a comprehensive QA program.

摘要

背景与目的

本研究旨在探讨放射治疗中体内质量保证计划的可行性与准确性。由于受照射组织的均匀性相当好,乳腺照射被视为一个相关的临床模型。

材料与方法

本研究基于对Leunens等人所描述方法的扩展(Leunens, G., van Dam, J., Dutreix, A.和van der Schueren, E. 体内剂量测定法在放射治疗中的质量保证。1. 入射剂量测量,一种可靠的方法。放射肿瘤学。17: 141 - 151, 1990; Leunens, G., van Dam, J., Dutreix, A.和van der Schueren, E. 体内剂量测定法在放射治疗中的质量保证。2. 靶区吸收剂量的测定。放射肿瘤学。19: 73 - 87, 1990; van Dam, J.和Marinello, G. 外照射放射治疗中的体内剂量测定方法。临床放射物理学。ESTRO手册第1号(Garant),1994),通过使用单独校准和校正的二极管测量入射和出射剂量来确定中心轴上任意点的吸收剂量。治疗准确性(δ)被量化为测量的等中心剂量与治疗计划系统(TPS)预期等中心剂量的比值。

结果

在一个有机玻璃平板模体上进行了初步研究以测试该方法,最终得到的δ频率分布均值为0.04±0.05%,标准差(SD)为0.83±0.04%。在体内研究中,在1年的时间里,101例接受两个切线野照射的患者被纳入研究方案。分析的患者摆位总数为421次,未进行任何校正时,δ分布的均值为 - 1.3±0.2%,标准差为2.7±0.1%。考虑到温度效应以及摆位误差(如源皮距准确性和二极管定位),可以实施一种离线校正方法,最终分布的均值为 - 1.9±0.2%,标准差为2.4±0.1%。检测并评估了偏差较大的个别病例,并尽可能采取了相应措施。

结论

该研究表明,放射技师可在精确的体内质量保证(QA)计划中轻松使用二极管,平均可达到1个标准差水平下3%的准确性。还可确定关注和行动水平,对治疗过程中的定位和形态变化进行仔细评估应成为全面QA计划的一部分。

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