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肺癌质子笔形束扫描放疗中射束特定相互作用效应的研究。

A study of the beam-specific interplay effect in proton pencil beam scanning delivery in lung cancer.

作者信息

Kang Minglei, Huang Sheng, Solberg Timothy D, Mayer Rulon, Thomas Andy, Teo Boon-Keng Kevin, McDonough James E, Simone Charles B, Lin Liyong

机构信息

a Department of Radiation Oncology , University of Pennsylvania , Philadelphia , PA , USA.

b Department of Radiation Oncology , University of California , San Francisco , CA , USA.

出版信息

Acta Oncol. 2017 Apr;56(4):531-540. doi: 10.1080/0284186X.2017.1293287. Epub 2017 Feb 25.

Abstract

BACKGROUND

For lung tumors with large motion amplitudes, the use of proton pencil beam scanning (PBS) can produce large dose errors. In this study, we assess under what circumstances PBS can be used to treat lung cancer patients who exhibit large tumor motion, based on the quantification of tumor motion and the dose interplay.

MATERIAL AND METHODS

PBS plans were optimized on average 4DCT datasets using a beam-specific PTV method for 10 consecutive patients with locally advanced non-small-cell-lung-cancer (NSCLC) treated with proton therapy to 6660/180 cGy. End inhalation (CT0) and end exhalation (CT50) were selected as the two extreme scenarios to acquire the relative stopping power ratio difference (Δrsp) for a respiration cycle. The water equivalent difference (ΔWET) per radiological path was calculated from the surface of patient to the iCTV by integrating the Δrsp of each voxel. The magnitude of motion of voxels within the target follows a quasi-Gaussian distribution. A motion index (MI (>5mm WET)), defined as the percentage of target voxels with an absolute integral ΔWET larger than 5 mm, was adopted as a metric to characterize interplay. To simulate the treatment process, 4D dose was calculated by accumulating the spot dose on the corresponding respiration phase to the reference phase CT50 by deformable image registration based on spot timing and patient breathing phase.

RESULTS

The study indicated that the magnitude of target underdose in a single fraction plan is proportional to the MI (p < .001), with larger motion equating to greater dose degradation and standard deviations. The target homogeneity, minimum, maximum and mean dose in the 4D dose accumulations of 37 fractions varied as a function of MI.

CONCLUSIONS

This study demonstrated that MI can predict the level of dose degradation, which potentially serves as a clinical decision tool to assess whether lung cancer patients are potentially suitable to receive PBS treatment.

摘要

背景

对于运动幅度较大的肺部肿瘤,使用质子笔形束扫描(PBS)会产生较大的剂量误差。在本研究中,我们基于肿瘤运动的量化和剂量相互作用,评估在何种情况下PBS可用于治疗肿瘤运动较大的肺癌患者。

材料与方法

使用特定射束的计划靶体积(PTV)方法,在平均4DCT数据集上对10例接受质子治疗至6660/180 cGy的局部晚期非小细胞肺癌(NSCLC)连续患者优化PBS计划。选择吸气末(CT0)和呼气末(CT50)作为两个极端情况,获取呼吸周期的相对阻止本领比差异(Δrsp)。通过对每个体素的Δrsp进行积分,从患者表面到内部临床靶体积(iCTV)计算每条放射路径的水等效差异(ΔWET)。靶区内体素的运动幅度遵循准高斯分布。采用运动指数(MI(>5mm WET)),定义为绝对积分ΔWET大于5 mm的靶体素百分比,作为表征相互作用的指标。为模拟治疗过程,基于射束点时间和患者呼吸相位,通过可变形图像配准将相应呼吸相位的射束点剂量累加到参考相位CT50,计算4D剂量。

结果

研究表明,单次分割计划中靶区剂量不足的幅度与MI成正比(p < 0.001),运动越大,剂量降解和标准差越大。37次分割的4D剂量累积中的靶区均匀性、最小、最大和平均剂量随MI而变化。

结论

本研究表明,MI可预测剂量降解水平,这有可能作为一种临床决策工具,用于评估肺癌患者是否有可能适合接受PBS治疗。

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