Lin Christie, Bradshaw Tyler, Perk Timothy, Harmon Stephanie, Eickhoff Jens, Jallow Ngoneh, Choyke Peter L, Dahut William L, Larson Steven, Humm John Laurence, Perlman Scott, Apolo Andrea B, Morris Michael J, Liu Glenn, Jeraj Robert
Department of Medical Physics, University of Wisconsin, Madison, Wisconsin.
Department of Radiology, University of Wisconsin, Madison, Wisconsin.
J Nucl Med. 2016 Dec;57(12):1872-1879. doi: 10.2967/jnumed.116.177295. Epub 2016 Jul 21.
F-NaF, a PET radiotracer of bone turnover, has shown potential as an imaging biomarker for assessing the response of bone metastases to therapy. This study aimed to evaluate the repeatability of F-NaF PET-derived SUV imaging metrics in individual bone lesions from patients in a multicenter study.
Thirty-five castration-resistant prostate cancer patients with multiple metastases underwent 2 whole-body (test-retest) F-NaF PET/CT scans 3 ± 2 d apart from 1 of 3 imaging sites. A total of 411 bone lesions larger than 1.5 cm were automatically segmented using an SUV threshold of 15 g/mL. Two levels of analysis were performed: lesion-level, in which measures were extracted from individual-lesion regions of interest (ROI), and patient-level, in which all lesions within a patient were grouped into a patient ROI for analysis. Uptake was quantified with SUV, SUV, and SUV Test-retest repeatability was assessed using Bland-Altman analysis, intraclass correlation coefficient (ICC), coefficient of variation, critical percentage difference, and repeatability coefficient. The 95% limit of agreement (LOA) of the ratio between test and retest measurements was calculated.
At the lesion level, the coefficient of variation for SUV, SUV, and SUV was 14.1%, 6.6%, and 25.5%, respectively. At the patient level, it was slightly smaller: 12.0%, 5.3%, and 18.5%, respectively. ICC was excellent (>0.95) for all SUV metrics. Lesion-level 95% LOA for SUV SUV, and SUV was (0.76, 1.32), (0.88, 1.14), and (0.63, 1.71), respectively. Patient-level 95% LOA was slightly narrower, at (0.79, 1.26), (0.89, 1.10), and (0.70, 1.44), respectively. We observed significant differences in the variance and sample mean of lesion-level and patient-level measurements between imaging sites.
The repeatability of SUV, SUV, and SUV for F-NaF PET/CT was similar between lesion- and patient-level ROIs. We found significant differences in lesion-level and patient-level distributions between sites. These results can be used to establish F-NaF PET-based criteria for assessing treatment response at the lesion and patient levels. F-NaF PET demonstrates repeatability levels useful for clinically quantifying the response of bone lesions to therapy.
F-NaF是一种骨转换的PET放射性示踪剂,已显示出作为评估骨转移对治疗反应的成像生物标志物的潜力。本研究旨在评估多中心研究中患者个体骨病变的F-NaF PET衍生SUV成像指标的可重复性。
35例患有多处转移的去势抵抗性前列腺癌患者在3个成像部位之一接受了2次全身(重测)F-NaF PET/CT扫描,间隔3±2天。使用15 g/mL的SUV阈值自动分割了总共411个大于1.5 cm的骨病变。进行了两个层面的分析:病变层面,从个体病变感兴趣区域(ROI)提取测量值;患者层面,将患者体内的所有病变分组为患者ROI进行分析。摄取量用SUV、SUV和SUV进行量化。使用Bland-Altman分析、组内相关系数(ICC)、变异系数、临界百分比差异和重复性系数评估重测可重复性。计算了测试和重测测量值之间比值的95%一致性界限(LOA)。
在病变层面,SUV、SUV和SUV的变异系数分别为14.1%、6.6%和25.5%。在患者层面,变异系数略小,分别为12.