Department for Radiation oncology and Experimental Cancer Research, Ghent University, De Pintelaan 185, B-9000 Gent, Belgium.
Phys Med Biol. 2013 Sep 21;58(18):6241-62. doi: 10.1088/0031-9155/58/18/6241. Epub 2013 Aug 22.
A quantitative comparison of two full three-dimensional (3D) gel dosimetry techniques was assessed in a clinical setting: radiochromic gel dosimetry with an in-house developed optical laser CT scanner and polymer gel dosimetry with magnetic resonance imaging (MRI). To benchmark both gel dosimeters, they were exposed to a 6 MV photon beam and the depth dose was compared against a diamond detector measurement that served as golden standard. Both gel dosimeters were found accurate within 4% accuracy. In the 3D dose matrix of the radiochromic gel, hotspot dose deviations up to 8% were observed which are attributed to the fabrication procedure. The polymer gel readout was shown to be sensitive to B0 field and B1 field non-uniformities as well as temperature variations during scanning. The performance of the two gel dosimeters was also evaluated for a brain tumour IMRT treatment. Both gel measured dose distributions were compared against treatment planning system predicted dose maps which were validated independently with ion chamber measurements and portal dosimetry. In the radiochromic gel measurement, two sources of deviations could be identified. Firstly, the dose in a cluster of voxels near the edge of the phantom deviated from the planned dose. Secondly, the presence of dose hotspots in the order of 10% related to inhomogeneities in the gel limit the clinical acceptance of this dosimetry technique. Based on the results of the micelle gel dosimeter prototype presented here, chemical optimization will be subject of future work. Polymer gel dosimetry is capable of measuring the absolute dose in the whole 3D volume within 5% accuracy. A temperature stabilization technique is incorporated to increase the accuracy during short measurements, however keeping the temperature stable during long measurement times in both calibration phantoms and the volumetric phantom is more challenging. The sensitivity of MRI readout to minimal temperature fluctuations is demonstrated which proves the need for adequate compensation strategies.
在临床环境中,对两种全三维(3D)凝胶剂量测定技术进行了定量比较:具有内部开发的光学激光 CT 扫描仪的放射比色凝胶剂量测定和磁共振成像(MRI)的聚合物凝胶剂量测定。为了对两种凝胶剂量计进行基准测试,将它们暴露于 6MV 光子束下,并将深度剂量与作为金标准的钻石探测器测量值进行比较。两种凝胶剂量计的准确性均在 4%以内。在放射比色凝胶的 3D 剂量矩阵中,观察到热点剂量偏差高达 8%,这归因于制造过程。聚合物凝胶读出被证明对 B0 场和 B1 场不均匀性以及扫描过程中的温度变化敏感。还评估了两种凝胶剂量计在脑肿瘤调强放疗治疗中的性能。将两种凝胶测量的剂量分布与治疗计划系统预测的剂量图进行比较,这些剂量图分别通过离子室测量和端口剂量学进行了独立验证。在放射比色凝胶测量中,可以确定两个偏差源。首先,在靠近体模边缘的体素簇中的剂量偏离了计划剂量。其次,由于凝胶中的不均匀性,存在 10%左右的剂量热点,限制了这种剂量测定技术的临床接受度。基于本文提出的胶束凝胶剂量计原型的结果,化学优化将成为未来的工作重点。聚合物凝胶剂量计能够在 5%的准确度内测量整个 3D 体积中的绝对剂量。已经采用了温度稳定技术来提高短时间测量的准确性,但是在校准体模和体积体模中保持长时间测量期间的温度稳定更具挑战性。MRI 读出对最小温度波动的敏感性证明了需要适当的补偿策略。