Department of Radiation Oncology, Saitama Medical University International Medical Center, 1397-1 Yamane, Hidaka, Saitama 350-1298, Japan.
Department of Oncology, Institute of Biomedical & Health Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima 734-8551, Japan.
Phys Med. 2018 Sep;53:145-152. doi: 10.1016/j.ejmp.2018.08.010. Epub 2018 Sep 11.
The aim of this study was to develop an end-to-end postal audit test to examine the coincidence between the imaging isocenter and treatment beam isocenter of the image guided radiotherapy (IGRT) linac system for Japan Clinical Oncology Group (JCOG) trials, as a part of IGRT credentialing of institutions participating in JCOG trials.
We developed an end-to-end postal audit test to verify radiation positional errors associated with IGRT techniques. This test is intended for simulating a clinical IGRT flow and uses a static cubic phantom measuring 15 × 15 × 15 cm and weighing approximately 3.4 kg. The phantom has four gold fiducial markers and a spherical dummy target for setup, with known shift values from the phantom center. Two pairs of Gafchromic RTQA2 films were inserted 5 mm from the phantom's anterior-posterior and right-left surfaces. Radiation positional errors at the isocenter were determined by analyzing the center of the radiation field on the films and the known shift values of the dummy target. The test was performed on 47 IGRT devices at 35 institutions.
Radiation positional errors were within acceptance levels (1 mm/1°) for 42 IGRT devices (89.4%) in the first check. Median time to complete IGRT credentialing was 11.5 days. This audit method was applicable for any radiotherapy machine with an IGRT device.
A postal audit test to verify radiation positional errors for JCOG trials was successfully developed. In the postal audit, all but one institution passed this credentialing item within two trials.
本研究旨在开发一种端到端的邮政审核测试,以检查图像引导放疗(IGRT)直线加速器系统的成像等中心点与治疗射束等中心点之间的一致性,作为参与日本临床肿瘤学组(JCOG)试验的机构进行 IGRT 认证的一部分。
我们开发了一种端到端的邮政审核测试,以验证与 IGRT 技术相关的辐射位置误差。该测试旨在模拟临床 IGRT 流程,使用一个静态立方体体模,尺寸为 15×15×15cm,重量约为 3.4kg。体模有四个金基准标记和一个用于设置的球形虚拟目标,其相对于体模中心的偏移值是已知的。两对 Gafchromic RTQA2 胶片插入体模前-后和右-左表面 5mm 处。通过分析胶片上辐射场的中心和虚拟目标的已知偏移值来确定等中心点的辐射位置误差。该测试在 35 个机构的 47 个 IGRT 设备上进行。
在第一次检查中,42 台 IGRT 设备(89.4%)的辐射位置误差在可接受范围内(1mm/1°)。完成 IGRT 认证的中位时间为 11.5 天。这种审核方法适用于任何带有 IGRT 设备的放射治疗机。
成功开发了一种用于验证 JCOG 试验辐射位置误差的邮政审核测试。在邮政审核中,所有机构(除一家外)都在两次试验内通过了这一认证项目。