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Direct parametric estimation of blood flow in abdominal PET/CT within an EM reconstruction framework

机译:在EM重建框架内直接参数估计腹部PET / CT中的血流

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Parametric estimation of perfusion using [15O]-H2O is an important biomarker for assessing treatment response in oncology clinical trials involving anti-vascular and anti-angiogenic agents. Traditionally the set of dynamic images are reconstructed independently, followed by post-reconstruction kinetic modelling. This methodology results in sub-optimal and often noisy end point parameters if voxel-by-voxel kinetic modelling is used. In [15O]-H2O scans, the extremely short temporal frames and the rapid decay of the tracer results in further signal-to-noise ratio (SNR) reduction. Direct 4-D reconstruction methods have the potential to reduce noise and improve parameter estimates by combining image reconstruction and kinetic modelling in a unified process. In this work we implement a direct parametric reconstruction using an EM framework and apply it on a real [15O]-H2O PET/CT dataset to derive parametric images of perfusion (f), clearance rate (k2) and fractional blood volume (Va). Results show substantial variance reduction both in perfusion and k2 images compared to the post-reconstruction kinetic analysis, especially in areas of increased perfusion. This results in increased tumour-to-background contrast and improved delineation of organ boundaries. Although further analysis in needed, direct reconstruction methods have the potential to be applied in a wide variety of oncology PET/CT studies with the improvements highly depended on the tracer and the system under study.
机译:使用[ 15 o] -h 2 O是灌注的参数估计是一种重要的生物标志物,用于评估涉及抗血管和抗血管生成剂的肿瘤临床试验中的治疗反应。传统上,该组动态图像独立重建,然后是重建后动力学建模。如果使用Voxel-u-Voxel动力学建模,则该方法导致次优和通常嘈杂的终点参数。扫描的[ 15 O] -h 扫描仪的快速衰减导致更新的信噪比(SNR)减少。通过在统一过程中组合图像重建和动力学建模,直接4-D重建方法具有降低噪声并改善参数估计。在这项工作中,我们使用EM框架实现直接参数重建,并将其应用于真实[ 15 o] -h 2 O PET / CT数据集以推导参数图像灌注(F),间隙(K 2 )和分数血容量(V A )。结果表明,与重建后动力学分析相比,灌注和K 2 图像中的差异减少了显着的差异,尤其是在灌注增加的区域。这导致增加肿瘤到背景对比度和改善器官界限的描绘。尽管所需的进一步分析,但直接重建方法具有在各种肿瘤宠物/ CT研究中应用的可能性,其改进高度依赖于示踪剂和正在研究的系统。

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