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Effect of Patient Set-up and Respiration motion on Defining Biological Targets for Image-Guided Targeted Radiotherapy.

机译:病人准备和呼吸运动对以图像为导向的靶向放射治疗的生物学目标的定义。

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摘要

Identification and monitoring of sub-tumor targets will be a critical step for optimal design and evaluation of cancer therapies in general and biologically targeted radiotherapy (dose-painting) in particular. Quantitative PET imaging may be an important tool for these applications. Currently radiotherapy planning accounts for tumor motion by applying geometric margins. These margins create a motion envelope to encompass the most probable positions of the tumor, while also maintaining the appropriate tumor control and normal tissue complication probabilities. This motion envelope is effective for uniform dose prescriptions where the therapeutic dose is conformed to the external margins of the tumor. However, much research is needed to establish the equivalent margins for non-uniform fields, where multiple biological targets are present and each target is prescribed its own dose level. Additionally, the size of the biological targets and close proximity make it impractical to apply planning margins on the sub-tumor level. Also, the extent of high dose regions must be limited to avoid excessive dose to the surrounding tissue. As such, this research project is an investigation of the uncertainty within quantitative PET images of moving and displaced dose-painting targets, and an investigation of the residual errors that remain after motion management. This included characterization of the changes in PET voxel-values as objects are moved relative to the discrete sampling interval of PET imaging systems (SPECIFIC AIM 1). Additionally, the repeatability of PET distributions and the delineating dose-painting targets were measured (SPECIFIC AIM 2). The effect of imaging uncertainty on the dose distributions designed using these images (SPECIFIC AIM 3) has also been investigated. This project also included analysis of methods to minimize motion during PET imaging and reduce the dosimetric impact of motion/position-induced imaging uncertainty (SPECIFIC AIM 4).
机译:识别和监测亚肿瘤靶标将是优化癌症治疗方法的最佳设计和评估的关键步骤,该方法尤其适用于一般的生物靶向放疗(剂量涂装)。定量PET成像可能是这些应用程序的重要工具。当前,放射治疗计划通过应用几何边界来考虑肿瘤运动。这些边缘形成运动包络线以涵盖肿瘤的最可能位置,同时还保持适当的肿瘤控制和正常组织并发症的可能性。该运动包络对于治疗剂量与肿瘤的外部边缘一致的均匀剂量处方有效。但是,需要进行大量研究来为非均匀区域建立等效边界,在该区域中存在多个生物学目标,并且每个目标都有自己的剂量水平。另外,生物靶标的大小和紧密接近使得在亚肿瘤水平上应用计划裕度不切实际。同样,必须限制高剂量区域的范围,以避免对周围组织的过量剂量。因此,该研究项目是对运动和位移剂量绘画目标的定量PET图像内的不确定性进行调查,并对运动管理后残留的残留误差进行调查。这包括表征对象相对于PET成像系统的离散采样间隔移动时PET体素值的变化(特定目的1)。此外,还测量了PET分布的可重复性和轮廓描绘剂量目标(规范目标2)。还研究了成像不确定性对使用这些图像设计的剂量分布的影响(SPECIFIC AIM 3)。该项目还包括分析方法,以最大程度地减少PET成像过程中的运动并减少运动/位置引起的成像不确定性对剂量的影响(SPECIFIC AIM 4)。

著录项

  • 作者

    McCall, Keisha C.;

  • 作者单位

    The University of Wisconsin - Madison.;

  • 授予单位 The University of Wisconsin - Madison.;
  • 学科 Health Sciences Radiology.;Physics Radiation.
  • 学位 Ph.D.
  • 年度 2011
  • 页码 122 p.
  • 总页数 122
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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