Palmer Antony L, Bradley David, Nisbet Andrew
University of Surrey.
J Appl Clin Med Phys. 2014 Jul 8;15(4):4854. doi: 10.1120/jacmp.v15i4.4854.
The measurement of dose distributions in clinical brachytherapy, for the purpose of quality control, commissioning or dosimetric audit, is challenging and requires development. Radiochromic film dosimetry with a commercial flatbed scanner may be suitable, but careful methodologies are required to control various sources of uncertainty. Triple-channel dosimetry has recently been utilized in external beam radiotherapy to improve the accuracy of film dosimetry, but its use in brachytherapy, with characteristic high maximum doses, steep dose gradients, and small scales, has been less well researched. We investigate the use of advanced film dosimetry techniques for brachytherapy dosimetry, evaluating uncertainties and assessing the mitigation afforded by triple-channel dosimetry. We present results on postirradiation film darkening, lateral scanner effect, film surface perturbation,film active layer thickness, film curling, and examples of the measurement of clinical brachytherapy dose distributions. The lateral scanner effect in brachytherapy film dosimetry can be very significant, up to 23% dose increase at 14 Gy, at ± 9 cm lateral from the scanner axis for simple single-channel dosimetry. Triple-channel dosimetry mitigates the effect, but still limits the useable width of a typical scanner to less than 8 cm at high dose levels to give dose uncertainty to within 1%. Triple-channel dosimetry separates dose and dose-independent signal components, and effectively removes disturbances caused by film thickness variation and surface perturbations in the examples considered in this work. The use of reference dose films scanned simultaneously with brachytherapy test films is recommended to account for scanner variations from calibration conditions. Postirradiation darkening, which is a continual logarithmic function with time, must be taken into account between the reference and test films. Finally, films must be flat when scanned to avoid the Callier-like effects and to provide reliable dosimetric results. We have demonstrated that radiochromic film dosimetry with GAFCHROMIC EBT3 film and a commercial flatbed scanner is a viable method for brachytherapy dose distribution measurement, and uncertainties may be reduced with triple-channel dosimetry and specific film scan and evaluation methodologies.
为了进行质量控制、调试或剂量学审核,在临床近距离放射治疗中测量剂量分布具有挑战性且需要改进。使用商用平板扫描仪进行放射变色胶片剂量测定可能是合适的,但需要谨慎的方法来控制各种不确定性来源。三通道剂量测定法最近已用于外照射放疗,以提高胶片剂量测定的准确性,但其在近距离放射治疗中的应用研究较少,因为近距离放射治疗具有高最大剂量、陡峭剂量梯度和小尺度的特点。我们研究了先进的胶片剂量测定技术在近距离放射治疗剂量测定中的应用,评估了不确定性,并评估了三通道剂量测定法所提供的缓解效果。我们展示了辐照后胶片变黑、横向扫描仪效应、胶片表面扰动、胶片活性层厚度、胶片卷曲的结果,以及临床近距离放射治疗剂量分布测量的示例。在近距离放射治疗胶片剂量测定中,横向扫描仪效应可能非常显著,对于简单的单通道剂量测定,在距扫描仪轴横向±9 cm处,在14 Gy时剂量增加高达23%。三通道剂量测定法减轻了这种效应,但在高剂量水平下,仍将典型扫描仪的可用宽度限制在小于8 cm以内,以使剂量不确定性在1%以内。三通道剂量测定法分离了剂量和与剂量无关的信号成分,并有效地消除了本研究中所考虑示例中由胶片厚度变化和表面扰动引起的干扰。建议使用与近距离放射治疗测试胶片同时扫描的参考剂量胶片,以考虑与校准条件不同的扫描仪变化。辐照后变黑是一个随时间连续变化的对数函数,在参考胶片和测试胶片之间必须予以考虑。最后,扫描时胶片必须平整,以避免类似卡利埃效应,并提供可靠的剂量学结果。我们已经证明,使用GAFCHROMIC EBT3胶片和商用平板扫描仪进行放射变色胶片剂量测定是测量近距离放射治疗剂量分布的一种可行方法,并且通过三通道剂量测定法以及特定的胶片扫描和评估方法可以降低不确定性。