Wulf Jörn, Hädinger Ulrich, Oppitz Ulrich, Thiele Wibke, Flentje Michael
Department of Radiotherapy, University of Würzburg, Josef-Schneider-Strasse 11, D-97080 Würzburg, Germany.
Radiother Oncol. 2003 Feb;66(2):141-50. doi: 10.1016/s0167-8140(02)00372-9.
Previous analyses of target reproducibility in extracranial stereotactic radiotherapy have revealed standard security margins for planning target volume (PTV) definition of 5mm in axial and 5-10mm in longitudinal direction. In this study the reproducibility of the clinical target volume (CTV) of lung and liver tumors within the PTV over the complete course of hypofractionated treatment is evaluated. The impact of target mobility on dose to the CTV is assessed by dose-volume histograms (DVH).
Twenty-two pulmonary and 21 hepatic targets were treated with three stereotactic fractions of 10 Gy to the PTV-enclosing 100%-isodose with normalization to 150% at the isocenter. A conformal dose distribution was related to the PTV, which was defined by margins of 5-10mm added to the CTV. Prior to each fraction a computed tomography (CT)-simulation over the complete target volume was performed resulting in a total of 60 CT-simulations for lung and 58 CT-simulations for hepatic targets. The CTV from each CT-simulation was segmented and matched with the CT-study used for treatment planning. A DVH of the simulated CTV was calculated for each fraction. The target coverage (TC) of dose to the simulated CTV was defined as the proportion of the CTV receiving at least the reference dose (100%).
A decrease of TC to <95% was found in 3/60 simulations (5%) of pulmonary and 7/58 simulations (12%) of hepatic targets. In two of 22 pulmonary targets (9%) and in four of 21 hepatic targets (19%) a TC of <95% occurred in at least one fraction. At risk for a decreased TC <95% were pulmonary targets with increased breathing mobility and hepatic targets with a CTV exceeding 100 cm(3).
Target reproducibility was precise within the reference isodose in 91% of lung and 81% of liver tumors with a TC of the complete CTV >or=95% at each fraction of treatment. Pulmonary targets with increased breathing mobility and liver tumors >100 cm(3) are at risk for target deviation exceeding the standard security margins for PTV-definition at least for one fraction and require individual evaluation of sufficient margins.
以往对颅外立体定向放射治疗中靶区可重复性的分析表明,在轴向方向上计划靶区(PTV)定义的标准安全边界为5mm,在纵向方向上为5 - 10mm。在本研究中,评估了在短疗程分割治疗的整个过程中,PTV内肺和肝肿瘤临床靶区(CTV)的可重复性。通过剂量体积直方图(DVH)评估靶区移动性对CTV剂量的影响。
对22个肺部靶区和21个肝脏靶区进行治疗,给予PTV三次立体定向分割剂量,每次10Gy,PTV包绕100%等剂量线,在等中心归一化至150%。将适形剂量分布与PTV相关联,PTV由在CTV基础上增加5 - 10mm的边界来定义。在每次分割治疗前,对整个靶区进行计算机断层扫描(CT)模拟,肺部靶区共进行60次CT模拟,肝脏靶区进行58次CT模拟。对每次CT模拟得到的CTV进行分割,并与用于治疗计划的CT研究进行匹配。计算每次分割治疗时模拟CTV的DVH。模拟CTV的剂量靶区覆盖度(TC)定义为接受至少参考剂量(100%)的CTV的比例。
在肺部靶区的60次模拟中有3次(5%)、肝脏靶区的58次模拟中有7次(12%)发现TC降至<95%。在22个肺部靶区中有2个(9%)、21个肝脏靶区中有4个(19%)至少在一次分割治疗中出现TC<95%。呼吸移动性增加的肺部靶区和CTV超过100 cm³的肝脏靶区有TC降至<95%的风险。
在每次分割治疗时,91%的肺部肿瘤和81%的肝脏肿瘤在参考等剂量线内靶区可重复性良好,整个CTV的TC≥95%。呼吸移动性增加的肺部靶区和体积>100 cm³的肝脏肿瘤至少在一次分割治疗中有靶区偏差超过PTV定义的标准安全边界的风险,需要对足够的边界进行个体化评估。