Ruschin Mark, Sixel Katharina E
Department of Medical Biophysics, University of Toronto, Ontario, Canada.
Med Phys. 2002 Aug;29(8):1698-709. doi: 10.1118/1.1495864.
Radiation dose escalation may be a means to increase the local control rate of inoperable lung tumors. Treatment plans involve the creation of a uniform planning target volume (PTV) to ensure proper coverage despite patient breathing and setup error. This may lead to unnecessary radiation of normal tissue in shallow breathers or target underdosing for patients with excess internal motion. Therefore, the nature of tumor motion for each patient should be measured in 3D, something that cannot be done with CT alone. We have developed a method that acquires 2D real-time fluoroscopic images (loops) and coregisters them with 2D digitally reconstructed radiographs (DRR) formed from the CT scan. The limitations of CT to encompass motion can be overcome by merging the two modalities together. The accuracy of the coregistration method is tested with a stationary grid of radio-opaque markers at various spatial positions. The in-plane (at-depth) displacement between markers on the fluoroscopic image versus the DRR varies with position across the image due to slight misalignments between the x-ray source used in fluoroscopy and the virtual source used for the DRR relative to the test object. At clinically relevant positions, the maximum, measured in-plane displacement, is 1.1 mm. The method is applied to the thorax of an anthropomorphic phantom and a good fit is observed between the appearances of the bony anatomical structures on the coregistered image. Finally, a series of motion measurements are carried out on two oscillating cylindrical objects. The degree of motion as measured by fluoroscopy is accurate to within 1.0 mm, whereas the DRR is inconsistent in predicting motion. The coregistration of fluoroscopic loops with the DRR shows at what point within the oscillation the DRR fails to encompass motion. For any treatment site involving target motion, this real-time imaging is a useful asset in the planning stage.
增加辐射剂量可能是提高无法手术的肺部肿瘤局部控制率的一种方法。治疗计划包括创建一个统一的计划靶体积(PTV),以确保尽管存在患者呼吸和摆位误差仍能实现适当的覆盖。这可能会导致浅呼吸患者的正常组织受到不必要的辐射,或者内部运动过多的患者靶区剂量不足。因此,应该对每个患者肿瘤运动的性质进行三维测量,而仅靠CT无法做到这一点。我们开发了一种方法,该方法获取二维实时荧光透视图像(动态图像环),并将它们与由CT扫描形成的二维数字重建射线照片(DRR)进行配准。通过将这两种模式合并在一起,可以克服CT在涵盖运动方面的局限性。使用不透射线标记物的固定网格在不同空间位置测试配准方法的准确性。由于荧光透视中使用的X射线源与用于DRR的虚拟源相对于测试对象之间存在轻微错位,荧光透视图像上的标记物与DRR之间的平面内(深度方向)位移会随图像上的位置而变化。在临床相关位置,测量到的最大平面内位移为1.1毫米。该方法应用于拟人化体模的胸部,在配准图像上观察到骨解剖结构的外观之间匹配良好。最后,在两个振荡的圆柱形物体上进行了一系列运动测量。通过荧光透视测量的运动程度精确到1.0毫米以内,而DRR在预测运动方面不一致。荧光透视动态图像环与DRR的配准显示了DRR在振荡过程中的哪个点无法涵盖运动。对于任何涉及靶区运动的治疗部位,这种实时成像在计划阶段都是一项有用的资产。