Four-Dimensional Dose Reconstruction for Scanned Proton Therapy Using Liver 4DCT-MRI

被引:27
作者
Bernatowicz, Kinga [1 ,2 ]
Peroni, Marta [2 ]
Perrin, Rosalind [2 ]
Weber, Damien C. [1 ,3 ]
Lomax, Antony [1 ,2 ]
机构
[1] Swiss Fed Inst Technol, Dept Phys, Zurich, Switzerland
[2] Paul Scherrer Inst, Proton Therapy Ctr, CH-5232 Villigen, Switzerland
[3] Univ Zurich Hosp, Dept Radiat Oncol, CH-8091 Zurich, Switzerland
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2016年 / 95卷 / 01期
关键词
MOTION; RADIOTHERAPY; BEAM; SIMULATION; ARTIFACTS;
D O I
10.1016/j.ijrobp.2016.02.050
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Four-dimensional computed tomography-magnetic resonance imaging (4DCT-MRI) is an image-processing technique for simulating many 4DCT data sets from a static reference CT and motions extracted from 4DMRI studies performed using either volunteers or patients. In this work, different motion extraction approaches were tested using 6 liver cases, and a detailed comparison between 4DCT-MRI and 4DCT was performed. Methods and Materials: 4DCT-MRI has been generated using 2 approaches. The first approach used motion extracted from 4DMRI as being "most similar" to that of 4DCT from the same patient (subject-specific), and the second approach used the most similar motion obtained from a motion library derived from 4DMRI liver studies of 13 healthy volunteers (population-based). The resulting 4DCT-MRI and 4DCTs were compared using scanned proton 4D dose calculations (4DDC). Results: Dosimetric analysis showed that 93% +/- 8% of points inside the clinical target volume (CTV) agreed between 4DCT and subject-specific 4DCT-MRI (gamma analysis: 3%/3 mm). The population-based approach however showed lower dosimetric agreement with only 79% +/- 14% points in the CTV reaching the 3%/3 mm criteria. Conclusions: 4D CT-MRI extends the capabilities of motion modeling for dose calculations by accounting for realistic and variable motion patterns, which can be directly employed in clinical research studies. We have found that the subject-specific liver modeling appears more accurate than the population-based approach. The former is particularly interesting for clinical applications, such as improved target delineation and 4D dose reconstruction for patient-specific QA to allow for inter- and/or intrafractional plan corrections. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:216 / 223
页数:8
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