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基于扫描质子束的在线图像引导肿瘤追踪:一项综合模拟研究。

Online image guided tumour tracking with scanned proton beams: a comprehensive simulation study.

作者信息

Zhang Ye, Knopf A, Tanner C, Lomax A J

机构信息

Centre for Proton Therapy, Paul Scherrer Institut, Switzerland. Computer Vision Laboratory, ETH Zurich, Zurich, Switzerland.

出版信息

Phys Med Biol. 2014 Dec 21;59(24):7793-817. doi: 10.1088/0031-9155/59/24/7793.

Abstract

Tumour tracking with scanned particle beams potentially requires accurate 3D information on both tumour motion and related density variations. We have previously developed a model-based motion reconstruction method, which allows for the prediction of deformable motions from sparsely sampled surrogate motions tracked via an on-board imaging system (Zhang et al (2013 Phys. Med. Biol. 58 8621)). Here, we investigate the potential effectiveness of tumour tracking for scanned proton beam therapy using such an approach to guide scanned beam tracking, together with the effectiveness of 're-tracking' for reducing residual motion effects due to tracking uncertainties. Three different beam tracking strategies (2D, 2D deformable and 3D) have been applied to three different liver motion cases, with mean magnitudes ranging from 10-20 mm. All simulations have been performed using simulated 4DCTs derived from 4DMRI datasets, whereby inter-breath-cycle motion variability is taken into account. The results show that, without beam tracking, large interplay effects are observed for all motion cases, resulting in CTV D5-95 values of 34.9/58.5/79.4% for the three cases, respectively. These can be reduced to 16.9/18.8/29.1% with 2D tracking, to 15.5/17.9/23.3% with 2D deformable tracking and to 15.1/17.8/21.0% with 3D tracking. Clear 'inverse interplay' effects have also been observed in the proximal portion of the field. However, with three-times re-tracking, D5-95 for the largest motions (20 mm) can be reduced to 13.0/12.8% for 2D and 3D tracking, respectively, and 'hot spots' resulting from the 'inverse interplay' effect can be substantially reduced. In summary, we have found that, for motions over 10 mm, tracking alone cannot fully mitigate motion effects, and can lead to substantially increased doses to normal tissues in the entrance path of the field. However, three-times re-tracking substantially improves the effectiveness of all types of beam tracking, with substantial advantages of 3D over 2D re-tracking only being observed for the largest motion scenario investigated.

摘要

利用扫描粒子束进行肿瘤追踪可能需要肿瘤运动及相关密度变化的精确三维信息。我们之前开发了一种基于模型的运动重建方法,该方法能够根据通过机载成像系统追踪到的稀疏采样替代运动来预测可变形运动(Zhang等人,《物理医学与生物学》,2013年,第58卷,第8621页)。在此,我们研究了使用这种方法来引导扫描束追踪在扫描质子束治疗中进行肿瘤追踪的潜在有效性,以及“重新追踪”对于减少由于追踪不确定性导致的残余运动影响的有效性。三种不同的束追踪策略(二维、二维可变形和三维)已应用于三种不同的肝脏运动病例,平均幅度范围为10 - 20毫米。所有模拟均使用从4D MRI数据集导出的模拟4DCT进行,其中考虑了呼吸周期之间的运动变异性。结果表明,在没有束追踪的情况下,所有运动病例均观察到较大的相互作用效应,三种病例的CTV D5 - 95值分别为34.9/58.5/79.4%。二维追踪可将其降至16.9/18.8/29.1%,二维可变形追踪可降至15.5/17.9/23.3%,三维追踪可降至15.1/17.8/21.0%。在射野近端也观察到了明显的“反向相互作用”效应。然而,经过三次重新追踪后,对于最大运动(20毫米),二维和三维追踪的D5 - 95分别可降至13.0/12.8%,并且由“反向相互作用”效应产生的“热点”可大幅减少。总之,我们发现,对于超过10毫米的运动,仅追踪不能完全减轻运动影响,并且可能导致射野入射路径中正常组织的剂量大幅增加。然而,三次重新追踪显著提高了所有类型束追踪的有效性,仅在研究的最大运动场景中观察到三维重新追踪相对于二维重新追踪具有显著优势。

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