The dose accumulation and the impact of deformable image registration on dose reporting parameters in a moving patient undergoing proton radiotherapy

被引:1
|
作者
Razdevsek, Gasper [1 ]
Simoncic, Urban [1 ,2 ]
Snoj, Luka [1 ,2 ]
Studen, Andrej [1 ,2 ]
机构
[1] Univ Ljubljana, Fac Math & Phys, Jadranska 19, SI-1000 Ljubljana, Slovenia
[2] Jozef Stefan Inst, Ljubljana, Slovenia
关键词
proton therapy; adaptive therapy; MCNP6; dose distribution measurement; Monte-Carlo; dose homogeneity; image registration; RADIATION-THERAPY; CANCER; MOTION; DELIVERY;
D O I
10.2478/raon-2022-0016
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction Potential changes in patient anatomy during proton radiotherapy may lead to a deviation of the delivered dose. A dose estimate can be computed through a deformable image registration (DIR) driven dose accumulation. The present study evaluates the accumulated dose uncertainties in a patient subject to an inadvertent breathing associated motion. Materials and methods A virtual lung tumour was inserted into a pair of single participant landmark annotated computed tomography images depicting opposite breathing phases, with the deep inspiration breath-hold the planning reference and the exhale the off-reference geometry. A novel Monte Carlo N-Particle, Version 6 (MCNP6) dose engine was developed, validated and used in treatment plan optimization. Three DIR methods were compared and used to transfer the exhale simulated dose to the reference geometry. Dose conformity and homogeneity measures from International Committee on Radioactivity Units and Measurements (ICRU) reports 78 and 83 were evaluated on simulated dose distributions registered with different DIR algorithms. Results The MCNP6 dose engine handled patient-like geometries in reasonable dose calculation times. All registration methods were able to align image associated landmarks to distances, comparable to voxel sizes. A moderate deterioration of ICRU measures was encountered in comparing doses in on and off-reference anatomy. There were statistically significant DIR driven differences in ICRU measures, particularly a 10% difference in the relative D-98% for planning tumour volume and in the 3 mm/3% gamma passing rate. Conclusions T he dose accumulation over two anatomies resulted in a DIR driven uncertainty, important in reporting the associated ICRU measures for quality assurance.
引用
收藏
页码:248 / 258
页数:11
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