Validation and application of a fast Monte Carlo algorithm for assessing the clinical impact of approximations in analytical dose calculations for pencil beam scanning proton therapy

被引:33
|
作者
Huang, Sheng [1 ,2 ]
Souris, Kevin [3 ,4 ]
Li, Siyang [1 ]
Kang, Minglei [1 ]
Montero, Ana Maria Barragan [3 ,4 ]
Janssens, Guillaume [5 ]
Lin, Alexander [1 ]
Garver, Elizabeth [1 ]
Ainsley, Christopher [1 ]
Taylor, Paige [6 ]
Xiao, Ying [1 ]
Lin, Liyong [1 ,7 ]
机构
[1] Univ Penn, Dept Radiat Oncol, 3400 Civ Cent Blvd, Philadelphia, PA 19104 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Med Phys, 1275 York Ave, New York, NY 10065 USA
[3] Catholic Univ Louvain, Inst Rech Expt & Clin, Ctr Mol Imaging & Expt Radiotherapy, Ave Hippocrate 54, B-1200 Brussels, Belgium
[4] Catholic Univ Louvain, ICTEAM Inst, B-1348 Louvain La Neuve, Belgium
[5] Adv Technol Grp Ion Beam Applicat SA, Louvain La Neuve, Belgium
[6] Univ Texas MD Anderson Canc Ctr, Imaging & Radiat Oncol Core Houston Qual Assuranc, 8060 El Rio St, Houston, TX 77054 USA
[7] Emory Univ, Winship Canc Inst, Dept Radiat Oncol, 1365 Clifton Rd, Atlanta, GA 30322 USA
关键词
fast Monte Carlo; Monte Carlo; pencil beam scanning; proton therapy; TRACK-REPEATING ALGORITHM; CALCULATION ACCURACY; RANGE UNCERTAINTIES; SIMULATION; IMPLEMENTATION; DELIVERY; SYSTEM; PHOTON; SIZE;
D O I
10.1002/mp.13231
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose Monte Carlo (MC) dose calculation is generally superior to analytical dose calculation (ADC) used in commercial TPS to model the dose distribution especially for heterogeneous sites, such as lung and head/neck patients. The purpose of this study was to provide a validated, fast, and open-source MC code, MCsquare, to assess the impact of approximations in ADC on clinical pencil beam scanning (PBS) plans covering various sites. Methods First, MCsquare was validated using tissue-mimicking IROC lung phantom measurements as well as benchmarked with the general purpose Monte Carlo TOPAS for patient dose calculation. Then a comparative analysis between MCsquare and ADC was performed for a total of 50 patients with 10 patients per site (including liver, pelvis, brain, head-and-neck, and lung). Differences among TOPAS, MCsquare, and ADC were evaluated using four dosimetric indices based on the dose-volume histogram (target Dmean, D95, homogeneity index, V95), a 3D gamma index analysis (using 3%/3 mm criteria), and estimations of tumor control probability (TCP). Results Comparison between MCsquare and TOPAS showed less than 1.8% difference for all of the dosimetric indices/TCP values and resulted in a 3D gamma index passing rate for voxels within the target in excess of 99%. When comparing ADC and MCsquare, the variances of all the indices were found to increase as the degree of tissue heterogeneity increased. In the case of lung, the D95s for ADC were found to differ by as much as 6.5% from the corresponding MCsquare statistic. The median gamma index passing rate for voxels within the target volume decreased from 99.3% for liver to 75.8% for lung. Resulting TCP differences can be large for lung (<= 10.5%) and head-and-neck (<= 6.2%), while smaller for brain, pelvis and liver (<= 1.5%). Conclusions Given the differences found in the analysis, accurate dose calculation algorithms such as Monte Carlo simulations are needed for proton therapy, especially for disease sites with high heterogeneity, such as head-and-neck and lung. The establishment of MCsquare can facilitate patient plan reviews at any institution and can potentially provide unbiased comparison in clinical trials given its accuracy, speed and open-source availability.
引用
收藏
页码:5631 / 5642
页数:12
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