目的:为了确定不同医学物理学家的影响,光子能量,治疗计划系统和治疗机器对样本前列腺癌病例的外部射束放射治疗剂量分布的影响。
方法:包含计划目标体积1(PTV1)前列腺和精囊(单剂量[SD]1.8Gy,总剂量[TD]59.4Gy),PTV2前列腺(同时整合增强[SIB],SD2.0Gy,TD66Gy),PTV3前列腺和精囊入路(SD1.8Gy,TD73.8Gy/80.4GySIB)以及处于危险中的器官(OAR:直肠,膀胱,股骨头,肠,anus)被提供给德国医学物理学会的任务组IMRT(调强放射治疗)的成员。目的是计算PTV1和PTV2的一种联合治疗计划(TP),以及PTV3的单独治疗计划。剂量体积直方图(DVH),不同的剂量值,合格指数(CI),同质性指数(HI),使用梯度指数(GI)和新的“优于平均分”来分析剂量分布。
结果:共有44个机构参与了这项研究,并提交了PTV的可接受剂量分布。然而,有统计学上的显著差异,特别是对于OAR的剂量,比如直肠,膀胱和股骨头。通过等剂量分布的视觉检查不容易检测到治疗计划之间的差异。最大剂量可发生在PTV之外。即使评分指数已经公布,需要新的“优于平均评分”来确定一个同时最小化所有OAR剂量的计划。
结论:不同的医学物理学家或剂量学家,光子能量,治疗计划系统,和治疗机器对产生的剂量分布有影响。然而,只有在比较DVH时,差异才会变得明显,分析剂量值,比较CI,HI,GI,以及检查每个平面的剂量分布。引入了新的评分,以确定同时向所有OAR提供低剂量的治疗计划。需要进行这种机构间和机构内的比较研究,以探索不同的治疗计划策略;然而,“最佳”治疗计划仍然没有自动解决方案。
OBJECTIVE: To determine the influence of different medical physicists, photon energies, treatment planning systems and treatment machines on the resulting external beam radiotherapy dose distribution for a sample prostate cancer
case.
METHODS: A pre-contoured computed tomography (CT) dataset containing planning target volume 1 (PTV1) prostate and seminal vesicles (single dose [SD] 1.8 Gy, total dose [TD] 59.4 Gy), PTV2 prostate (simultaneously integrated boost [SIB], SD 2.0 Gy, TD 66 Gy), PTV3 prostate and seminal vesicles approach (SD 1.8 Gy, TD 73.8 Gy/80.4 Gy SIB) as well as organs at risk (OAR: rectum, bladder, femoral heads, bowel, anus) was offered to the members of the task group IMRT (intensity-modulated radiation therapy) of the German Society for Medical Physics. The purpose was to calculate one combined treatment plan (TP) for PTV1 and PTV2, as well as a separate one for PTV3. Dose volume histograms (DVH), different dose values, conformity index (CI), homogeneity index (HI), gradient index (GI) and a new \"better than average score\" were used to analyse the dose distributions.
RESULTS: Altogether 44 institutions took part in this study and submitted acceptable dose distributions for the PTVs. However, there were statistically significant differences, especially for the doses administered to the OAR, such as rectum, bladder and femoral heads. Differences between the treatment plans were not easily detectable by visual inspection of the isodose distribution. Dose maxima may occur outside the PTV. Even though scoring indices are already published, the new \"better than average score\" was needed to identify a plan that minimises dose to all OAR simultaneously.
CONCLUSIONS: Different medical physicists or dosimetrists, photon energies, treatment planning systems, and treatment machines have an impact on the resulting dose distribution. However, the differences only become apparent when comparing DVH, analysing dose values, comparing CI, HI, GI, as well as reviewing the dose distribution in every single plane. A new score was introduced to identify treatment plans that simultaneously deliver a low dose to all OAR. Such inter- and intra-institutional comparison studies are needed to explore different treatment planning strategies; however, there is still no automatic solution for an \"optimal\" treatment plan.