Department of Statistics, School of Mathematical Sciences, University College Cork, Cork, Ireland.
Advanced Clinical Imaging Technology, Siemens Healthcare AG, Lausanne, Switzerland; and.
J Nucl Med. 2024 Jun 3;65(6):971-979. doi: 10.2967/jnumed.123.266686.
The purpose of this study was to examine a nonparametric approach to mapping kinetic parameters and their uncertainties with data from the emerging generation of dynamic whole-body PET/CT scanners. Dynamic PET F-FDG data from a set of 24 cancer patients studied on a long-axial-field-of-view PET/CT scanner were considered. Kinetics were mapped using a nonparametric residue mapping (NPRM) technique. Uncertainties were evaluated using an image-based bootstrapping methodology. Kinetics and bootstrap-derived uncertainties are reported for voxels, maximum-intensity projections, and volumes of interest (VOIs) corresponding to several key organs and lesions. Comparisons between NPRM and standard 2-compartment (2C) modeling of VOI kinetics are carefully examined. NPRM-generated kinetic maps were of good quality and well aligned with vascular and metabolic F-FDG patterns, reasonable for the range of VOIs considered. On a single 3.2-GHz processor, the specification of the bootstrapping model took 140 min; individual bootstrap replicates required 80 min each. VOI time-course data were much more accurately represented, particularly in the early time course, by NPRM than by 2C modeling constructs, and improvements in fit were statistically highly significant. Although F-FDG flux values evaluated by NPRM and 2C modeling were generally similar, significant deviations between vascular blood and distribution volume estimates were found. The bootstrap enables the assessment of quite complex summaries of mapped kinetics. This is illustrated with maximum-intensity maps of kinetics and their uncertainties. NPRM kinetics combined with image-domain bootstrapping is practical with large whole-body dynamic F-FDG datasets. The information provided by bootstrapping could support more sophisticated uses of PET biomarkers used in clinical decision-making for the individual patient.
本研究旨在探讨一种非参数方法,以利用新一代动态全身 PET/CT 扫描仪生成的数据来绘制动力学参数及其不确定性。考虑了一组 24 名癌症患者在长轴向视野 PET/CT 扫描仪上进行的动态 PET F-FDG 数据。使用非参数残差映射(NPRM)技术对动力学进行了映射。使用基于图像的自举方法评估不确定性。报告了体素、最大强度投影和与几个关键器官和病变相对应的感兴趣区域(VOI)的动力学和基于引导的不确定性。仔细检查了 NPRM 与 VOI 动力学的标准 2 室(2C)建模之间的比较。NPRM 生成的动力学图质量良好,与血管和代谢 F-FDG 模式对齐良好,适用于所考虑的 VOI 范围。在单个 3.2-GHz 处理器上,引导模型的规范需要 140 分钟;每个引导复制需要 80 分钟。与 2C 建模结构相比,NPRM 更准确地表示了 VOI 时程数据,特别是在早期时程,拟合的改进具有统计学意义上的显著提高。尽管通过 NPRM 和 2C 建模评估的 F-FDG 通量值通常相似,但在血管血液和分布容积估计方面发现了明显的偏差。引导使评估映射动力学的相当复杂的摘要成为可能。这通过动力学及其不确定性的最大强度图来说明。NPRM 动力学结合图像域引导是实用的,适用于大型全身动态 F-FDG 数据集。引导提供的信息可以支持在为个体患者进行临床决策时对 PET 生物标志物的更复杂使用。