Jafari Shakardokht M, Jordan Tom J, Distefano Gail, Bradley David A, Spyrou Nicholas M, Nisbet Andrew, Clark Catharine H
1 Department of Physics, University of Surrey, London, UK.
2 Radiology Department, Faculty of Medicine, Kabul Medical University, Kabul, Afghanistan.
Br J Radiol. 2015;88(1055):20140804. doi: 10.1259/bjr.20140804. Epub 2015 Aug 10.
To investigate the feasibility of using glass beads as novel thermoluminescent dosemeters (TLDs) for radiotherapy treatment plan verification.
Commercially available glass beads with a size of 1-mm thickness and 2-mm diameter were characterized as TLDs. Five clinical treatment plans including a conventional larynx, a conformal prostate, an intensity-modulated radiotherapy (IMRT) prostate and two stereotactic body radiation therapy (SBRT) lung plans were transferred onto a CT scan of a water-equivalent phantom (Solid Water(®), Gammex, Middleton, WI) and the dose distribution recalculated. The number of monitor units was maintained from the clinical plan and delivered accordingly. The doses determined by the glass beads were compared with those measured by a graphite-walled ionization chamber, and the respective expected doses were determined by the treatment-planning system (TPS) calculation.
The mean percentage difference between measured dose with the glass beads and TPS was found to be 0.3%, -0.1%, 0.4%, 1.8% and 1.7% for the conventional larynx, conformal prostate, IMRT prostate and each of the SBRT delivery techniques, respectively. The percentage difference between measured dose with the ionization chamber and glass bead was found to be -1.2%, -1.4%, -0.1%, -0.9% and 2.4% for the above-mentioned plans, respectively. The results of measured doses with the glass beads and ionization chamber in comparison with expected doses from the TPS were analysed using a two-sided paired t-test, and there was no significant difference at p < 0.05.
It is feasible to use glass-bead TLDs as dosemeters in a range of clinical plan verifications.
Commercial glass beads are utilized as low-cost novel TLDs for treatment-plan verification.
探讨使用玻璃微珠作为新型热释光剂量计(TLD)用于放射治疗计划验证的可行性。
将市售的厚度为1毫米、直径为2毫米的玻璃微珠作为TLD进行特性分析。将五个临床治疗计划,包括一个常规喉癌计划、一个适形前列腺癌计划、一个调强放射治疗(IMRT)前列腺癌计划和两个立体定向体部放射治疗(SBRT)肺癌计划,转移到水等效体模(Solid Water®,Gammex,米德尔顿,威斯康星州)的CT扫描图像上,并重新计算剂量分布。监测单位数量保持与临床计划一致并相应给予。将玻璃微珠测定的剂量与石墨壁电离室测量的剂量进行比较,并通过治疗计划系统(TPS)计算确定各自的预期剂量。
对于常规喉癌、适形前列腺癌、IMRT前列腺癌以及每种SBRT技术,玻璃微珠测量剂量与TPS之间的平均百分比差异分别为0.3%、-0.1%、0.4%、1.8%和1.7%。对于上述计划,电离室与玻璃微珠测量剂量之间的百分比差异分别为-1.2%、-1.4%、-0.1%、-0.9%和2.4%。使用双侧配对t检验分析玻璃微珠和电离室测量剂量与TPS预期剂量比较的结果,在p < 0.05时无显著差异。
在一系列临床计划验证中使用玻璃微珠TLD作为剂量计是可行的。
商业玻璃微珠被用作低成本的新型TLD进行治疗计划验证。