Department of Medical Physics, Apollo Proton Cancer Centre, Chennai, Tamil Nadu, India.
Department of Radiation Oncology, Apollo Proton Cancer Center, Chennai, Tamil Nadu, India.
Br J Radiol. 2021 Mar 1;94(1119):20201031. doi: 10.1259/bjr.20201031. Epub 2021 Feb 2.
To study dosimetric impact of random spot positioning errors on the clinical pencil beam scanning proton therapy plans.
IMPT plans of 10 patients who underwent proton therapy for tumors in brain or pelvic regions representing small and large volumes, respectively, were included in the study. Spot positioning errors of 1 mm, -1 mm or ±1 mm were introduced in these clinical plans by modifying the geometrical co-ordinates of proton spots using a script in the MATLAB programming environment. Positioning errors were simulated to certain numbers of (20%, 40%, 60%, 80%) randomly chosen spots in each layer of these treatment plans. Treatment plans with simulated errors were then imported back to the Raystation (Version 7) treatment planning system and the resultant dose distribution was calculated using Monte-Carlo dose calculation algorithm.Dosimetric plan evaluation parameters for target and critical organs of nominal treatment plans delivered for clinical treatments were compared with that of positioning error simulated treatment plans. For targets, D95% and D2% were used for the analysis. Dose received by optic nerve, chiasm, brainstem, rectum, sigmoid, and bowel were analyzed using relevant plan evaluation parameters depending on the critical structure. In case of intracranial lesions, the dose received by 0.03 cm volume (D) was analyzed for optic nerve, chiasm and brainstem. In rectum, the volume of it receiving a dose of 65 Gy(RBE) (V65) and 40 Gy(RBE) (V40) were compared between the nominal and error introduced plans. Similarly, V65 and V63 were analyzed for Sigmoid and V50 and V15 were analyzed for bowel.
The maximum dose variation in PTV D (1.88 %) was observed in a brain plan in which the target volume was the smallest (2.7 cm) among all 10 plans included in the study. This variation in D drops down to 0.3% for a sacral chordoma plan in which the PTV volume is significantly higher at 672 cm. The maximum difference in OARs in terms of absolute dose (D) was found in left optic nerve (9.81%) and the minimum difference was observed in brainstem (2.48%). Overall, the magnitude of dose errors in chordoma plans were less significant in comparison to brain plans.
The dosimetric impact of different error scenarios in spot positioning becomes more prominent for treatment plans involving smaller target volume compared to plans involving larger target volumes.
Provides information on the dosimetric impact of various possible spot positioning errors and its dependence on the tumor volume in intensity modulated proton therapy.
研究随机点定位误差对临床笔形束扫描质子治疗计划的剂量学影响。
纳入了 10 名接受脑部或骨盆区域肿瘤质子治疗的患者的 IMPT 计划,这些患者的肿瘤体积分别较小和较大。通过在 MATLAB 编程环境中使用脚本修改质子点的几何坐标,在这些临床计划中引入了 1mm、-1mm 或±1mm 的点定位误差。在这些治疗计划的每一层中,模拟了一定数量(20%、40%、60%、80%)随机选择的点的定位误差。然后将具有模拟误差的治疗计划导入 Raystation(版本 7)治疗计划系统,并使用蒙特卡罗剂量计算算法计算得到的剂量分布。将用于临床治疗的名义治疗计划的靶区和关键器官的剂量学计划评估参数与模拟定位误差的治疗计划进行比较。对于靶区,使用 D95%和 D2%进行分析。根据关键结构,使用相关计划评估参数分析视神经、视交叉、脑干、直肠、乙状结肠和肠道接受的剂量。对于颅内病变,分析视神经、视交叉和脑干的 0.03cm 体积(D)接受的剂量。在直肠中,比较名义计划和引入误差计划之间接受 65Gy(RBE)(V65)和 40Gy(RBE)(V40)剂量的体积。类似地,分析乙状结肠的 V65 和 V63,分析肠道的 V50 和 V15。
在所有纳入研究的 10 个计划中,靶区体积最小(2.7cm)的脑部计划中观察到 PTV D 的最大剂量变化(1.88%)。当靶区体积较大(672cm)时,在骶骨脊索瘤计划中,这种 D 的变化降至 0.3%。在绝对剂量(D)方面,OAR 最大差异出现在左侧视神经(9.81%),最小差异出现在脑干(2.48%)。总体而言,与脑部计划相比,脊索瘤计划中的剂量误差幅度较小。
与涉及较大靶区体积的计划相比,涉及较小靶区体积的调强质子治疗计划中不同的点定位误差的剂量学影响更为显著。
提供了有关各种可能的点定位误差及其在调强质子治疗中与肿瘤体积的关系的剂量学影响的信息。