A method using 4D dose accumulation to quantify the interplay effect in lung stereotactic body radiation therapy

多叶准直器 核医学 计算机科学 准直器 算法 数学 放射治疗 放射治疗计划 物理 医学 放射科 光学
作者
Carlos Huesa-Berral,Javier Burguete,Marta Moreno-Jiménez,Juan Diego Azcona
出处
期刊:Physics in Medicine and Biology [IOP Publishing]
卷期号:66 (3): 035025-035025 被引量:5
标识
DOI:10.1088/1361-6560/abd00f
摘要

Abstract The purpose of this study was to devise and evaluate a method to quantify the dosimetric uncertainty produced by the interplay between the movement of multileaf collimator and respiratory motion in lung stereotactic body radiation therapy. The method calculates the dose distribution for all control points from a dynamic treatment in all respiratory phases. The methodology includes some characteristics of a patient’s irregular breathing patterns. It selects, for each control point, the phases with maximum and minimum mean dose over the tumor and their corresponding adjacent phases, whenever necessary. According to this selection, the dose matrices from each control point are summed up to obtain two dose distributions in each phase, which are accumulated in the reference phase subsequently by deformable image registration (DIR). D 95 and D min , 0.035 cc were calculated over those accumulated dose distributions for Gross Tumor Volume (GTV), Planning Target Volume—based on Internal Target Volume approach—and Evaluation Target Volume (ETV), a novel concept that applies to 4D dose accumulation. With the ETV, DIR and interplay uncertainties are separated. The methodology also evaluated how variations in the breathing rate and field size affects the mean dose received by the GTV. The method was applied retrospectively in five patients treated with intensity modulated radiotherapy—minimum area defined by the leaves configuration at any control point was at least 4 cm 2 . Uncertainties in tumor coverage were small (in most patients, changes on D 95 and D min , 0.035 cc were below 2% for GTV and ETV) but significant over- and under-dosages near ETV, which can be accentuated by highly irregular breathing. Uncertainties in mean dose for GTV tended to decrease exponentially with increasing field size and were reduced by an increase of breathing rate. The implementation of this method would be helpful to assess treatment quality in patients with irregular breathing. Furthermore, it could be used to study interplay uncertainties when small field sizes are used.

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