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不规则呼吸运动及其对肺肿瘤剂量学影响的模拟研究。

A simulation study of irregular respiratory motion and its dosimetric impact on lung tumors.

机构信息

Department of Radiation Oncology, University of Pittsburgh Medical Center, Pittsburgh, PA 15232, USA.

出版信息

Phys Med Biol. 2011 Feb 7;56(3):845-59. doi: 10.1088/0031-9155/56/3/019. Epub 2011 Jan 17.

Abstract

This study is aimed at providing a dosimetric evaluation of the irregular motion of lung tumors due to variations in patients' respiration. Twenty-three lung cancer patients are retrospectively enrolled in this study. The motion of the patient clinical target volume is simulated and two types of irregularities are defined: characteristic and uncharacteristic motions. Characteristic irregularities are representative of random fluctuations in the observed target motion. Uncharacteristic irregular motion is classified as systematic errors in determination of the target motion during the planning session. Respiratory traces from measurement of patient abdominal motion are also used for the target motion simulations. Characteristic irregular motion was observed to cause minimal changes in target dosimetry with the largest effect of 2.5% ± 0.9% (1σ) reduction in the minimum target dose (D(min)) observed for targets that move 2 cm on average and exhibiting 50% amplitude variations within a session. However, uncharacteristic irregular motion introduced more drastic changes in the clinical target volume (CTV) dose; 4.1% ± 1.7% reduction for 1 cm motion and 9.6% ± 1.7% drop for 2 cm. In simulations with patients' abdominal motion, corresponding changes in target dosimetry were observed to be negligible (<0.1%). Only uncharacteristic irregular motion was identified as a clinically significant source of dosimetric uncertainty.

摘要

本研究旨在对由于患者呼吸变化导致的肺部肿瘤不规则运动进行剂量评估。回顾性纳入了 23 例肺癌患者。模拟了患者临床靶区的运动,并定义了两种不规则运动:特征性和非特征性运动。特征性不规则运动代表观察到的靶区运动中的随机波动。非特征性不规则运动被归类为在计划阶段确定靶区运动时的系统误差。还使用测量患者腹部运动的呼吸轨迹进行靶区运动模拟。特征性不规则运动导致靶区剂量学变化最小,最大效应为 2.5%±0.9%(1σ),观察到平均移动 2 cm 且在一次治疗中具有 50%幅度变化的靶区的最小靶区剂量(D(min))减少。然而,非特征性不规则运动导致临床靶区(CTV)剂量发生更剧烈的变化;1 cm 运动时减少 4.1%±1.7%,2 cm 时减少 9.6%±1.7%。在模拟患者腹部运动时,观察到靶区剂量学的相应变化可以忽略不计(<0.1%)。只有非特征性不规则运动被确定为剂量学不确定性的一个重要临床来源。

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