The clinical impact of uncertainties in the mean excitation energy of human tissues during proton therapy

被引:34
作者
Besemer, Abigail [1 ]
Paganetti, Harald [2 ]
Bednarz, Bryan [1 ]
机构
[1] Univ Wisconsin, Wisconsin Inst Med Res, Dept Med Phys, Madison, WI 53715 USA
[2] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Radiat Oncol, Boston, MA USA
关键词
SCATTERING CROSS-SECTIONS; ELECTRONIC STOPPING POWER; MONTE-CARLO SIMULATIONS; RANGE UNCERTAINTIES; ORGANIC-COMPOUNDS; ALPHA-PARTICLES; WATER; DISTRIBUTIONS; RADIOTHERAPY; BEAMS;
D O I
10.1088/0031-9155/58/4/887
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Uncertainties in the estimated mean excitation energies (I-values) needed for calculating proton stopping powers can be in the order of 10-15%, which introduces a fundamental limitation in the accuracy of proton range determination. Previous efforts have quantified shifts in proton depth dose distributions due to I-value uncertainties in water and homogenous tissue phantoms. This study is the first to quantify the clinical impact of I-value uncertainties on proton dose distributions within patient geometries. A previously developed Geant4 based Monte Carlo code was used to simulate a proton treatment plan for three patients (prostate, pancreases, and liver) with varying tissue I-values. A uniform variation study was conducted in which the tissue I-values were varied by +/- 5% and +/- 10% of the nominal values as well as a probabilistic variation study in which the I-values were randomly sampled according to a normal distribution with the mean equal to the nominal I-value and a standard deviation of 5 and 10% of the nominal values. Modification of tissue I-values impacted both the proton range and SOBP width. R-90 range shifts up to 7.7 mm (4.4.%) and R-80 range shifts up to 4.8 mm (1.9%) from the nominal range were recorded. Modulating the tissue I-values by 10% the nominal value resulted in up to a 3.5% difference mean dose in the target volumes and organs at risk compared to the nominal case. The range and dose differences were the largest for the deeper-seated prostate and pancreas cases. The treatments that were simulated with randomly sampled I-values resulted in range and dose differences that were generally within the upper and lower bounds set by the 10% uniform variations. This study demonstrated the impact of I-value uncertainties on patient dose distributions. Clearly, sub-millimeter precision in proton therapy would necessitate a reduction in I-value uncertainties to ensure an efficacious clinical outcome.
引用
收藏
页码:887 / 902
页数:16
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