Department of Physics "E. Pancini", Federico II University, 80126 Naples, Italy.
Centro Servizi Metrologici e Tecnologici Avanzati, Federico II University, 80146 Naples, Italy.
Sensors (Basel). 2023 Mar 30;23(7):3592. doi: 10.3390/s23073592.
Surface brachytherapy (BT) lacks standard quality assurance (QA) protocols. Commercially available treatment planning systems (TPSs) are based on a dose calculation formalism that assumes the patient is made of water, resulting in potential deviations between planned and delivered doses. Here, a method for treatment plan verification for skin surface BT is reported. Chips of thermoluminescent dosimeters (TLDs) were used for dose point measurements. High-dose-rate treatments were simulated and delivered through a custom-flap applicator provided with four fixed catheters to guide the Iridium-192 (Ir-192) source by way of a remote afterloading system. A flat water-equivalent phantom was used to simulate patient skin. Elekta TPS Oncentra Brachy was used for planning. TLDs were calibrated to Ir-192 through an indirect method of linear interpolation between calibration factors (CFs) measured for 250 kV X-rays, Cesium-137, and Cobalt-60. Subsequently, plans were designed and delivered to test the reproducibility of the irradiation set-up and to make comparisons between planned and delivered dose. The obtained CF for Ir-192 was (4.96 ± 0.25) μC/Gy. Deviations between measured and TPS calculated doses for multi-catheter treatment configuration ranged from -8.4% to 13.3% with an average of 0.6%. TLDs could be included in clinical practice for QA in skin BT with a customized flap applicator.
表面近距离治疗(BT)缺乏标准的质量保证(QA)协议。市售的治疗计划系统(TPS)基于剂量计算公式,假设患者由水组成,导致计划剂量和实际剂量之间存在潜在偏差。本文报道了一种皮肤表面 BT 治疗计划验证方法。使用热释光剂量计(TLD)芯片进行剂量点测量。通过带有四个固定导管的定制瓣状敷贴器模拟高剂量率治疗,并通过远程后装系统引导铱 192(Ir-192)源。使用平水等效体模模拟患者皮肤。采用 Elekta TPS Oncentra Brachy 进行规划。TLD 通过在为 250 kV X 射线、铯 137 和钴 60 测量的校准因子(CF)之间进行间接线性插值的方法对 Ir-192 进行校准。随后,设计并实施计划以测试照射设置的可重复性,并比较计划剂量和实际剂量。获得的 Ir-192 的 CF 值为(4.96 ± 0.25)μC/Gy。对于多导管治疗配置,测量剂量与 TPS 计算剂量之间的偏差范围为-8.4%至 13.3%,平均值为 0.6%。对于带有定制瓣状敷贴器的皮肤 BT,TLD 可用于临床 QA。