Holman Beverley F, Cuplov Vesna, Hutton Brian F, Groves Ashley M, Thielemans Kris
Institute of Nuclear Medicine, UCLH, 235 Euston Road (T-5), London, NW1 2BU, UK.
Phys Med Biol. 2016 Apr 21;61(8):3148-63. doi: 10.1088/0031-9155/61/8/3148. Epub 2016 Mar 23.
Accurate PET quantitation requires a matched attenuation map. Obtaining matched CT attenuation maps in the thorax is difficult due to the respiratory cycle which causes both motion and density changes. Unlike with motion, little attention has been given to the effects of density changes in the lung on PET quantitation. This work aims to explore the extent of the errors caused by pulmonary density attenuation map mismatch on dynamic and static parameter estimates. Dynamic XCAT phantoms were utilised using clinically relevant (18)F-FDG and (18)F-FMISO time activity curves for all organs within the thorax to estimate the expected parameter errors. The simulations were then validated with PET data from 5 patients suffering from idiopathic pulmonary fibrosis who underwent PET/Cine-CT. The PET data were reconstructed with three gates obtained from the Cine-CT and the average Cine-CT. The lung TACs clearly displayed differences between true and measured curves with error depending on global activity distribution at the time of measurement. The density errors from using a mismatched attenuation map were found to have a considerable impact on PET quantitative accuracy. Maximum errors due to density mismatch were found to be as high as 25% in the XCAT simulation. Differences in patient derived kinetic parameter estimates and static concentration between the extreme gates were found to be as high as 31% and 14%, respectively. Overall our results show that respiratory associated density errors in the attenuation map affect quantitation throughout the lung, not just regions near boundaries. The extent of this error is dependent on the activity distribution in the thorax and hence on the tracer and time of acquisition. Consequently there may be a significant impact on estimated kinetic parameters throughout the lung.
准确的PET定量分析需要匹配的衰减图。由于呼吸周期会导致运动和密度变化,因此在胸部获取匹配的CT衰减图很困难。与运动不同,肺部密度变化对PET定量分析的影响很少受到关注。这项工作旨在探讨肺部密度衰减图不匹配对动态和静态参数估计所造成的误差程度。利用动态XCAT体模,并使用胸部所有器官的临床相关(18)F-FDG和(18)F-FMISO时间-活度曲线来估计预期的参数误差。然后用5例特发性肺纤维化患者的PET/Cine-CT的PET数据对模拟进行验证。PET数据用从Cine-CT和平均Cine-CT获得的三个门控进行重建。肺部时间-活度曲线清楚地显示了真实曲线和测量曲线之间的差异,误差取决于测量时的整体活度分布。发现使用不匹配的衰减图产生的密度误差对PET定量准确性有相当大的影响。在XCAT模拟中,由于密度不匹配导致的最大误差高达25%。发现患者衍生的动力学参数估计值和极端门控之间的静态浓度差异分别高达31%和14%。总体而言,我们的结果表明,衰减图中与呼吸相关的密度误差会影响整个肺部的定量分析,而不仅仅是边界附近的区域。这种误差的程度取决于胸部的活度分布,因此取决于示踪剂和采集时间。因此,可能会对整个肺部的估计动力学参数产生重大影响。