Souvatzoglou M, Ziegler S I, Martinez M J, Busch R, Dzewas G, Schwaiger M, Bengel F
Nuklearmedizinische Klinik der Technischen Universität München, Ismaninger Strasse 22, 81675 Munich, Germany.
Eur J Nucl Med Mol Imaging. 2007 Mar;34(3):405-12. doi: 10.1007/s00259-006-0196-1. Epub 2006 Sep 5.
In PET/CT, CT-derived attenuation factors may influence standardised uptake values (SUVs) in tumour lesions and organs when compared with stand-alone PET. Therefore, we compared PET/CT-derived SUVs intra-individually in various organs and tumour lesions with stand-alone PET-derived SUVs.
Thirty-five patients with known or suspected cancer were prospectively included. Sixteen patients underwent FDG PET using an ECAT HR+scanner, and subsequently a second scan using a Biograph Sensation 16PET/CT scanner. Nineteen patients were scanned in the reverse order. All images were reconstructed with an iterative algorithm (OSEM). Suspected lesions were grouped as paradiaphragmatic versus distant from the diaphragm. Mean and maximum SUVs were also calculated for brain, lung, liver, spleen and vertebral bone. The attenuation coefficients (mu values) used for correction of emission data (bone, soft tissue, lung) in the two data sets were determined. A body phantom containing six hot spheres and one cold cylinder was measured using the same protocol as in patients.
Forty-six lesions were identified. There was a significant correlation of maximum and mean SUVs derived from PET and PET/CT for 14 paradiaphragmatic lesions (r=0.97 respectively; p<0.001 respectively) and for 32 lesions located distant from the diaphragm (r=0.87 and r=0.89 respectively; p<0.001 respectively). No significant differences were observed in the SUVs calculated with PET and PET/CT in the lesions or in the organs. In the phantom, radioactivity concentration in spheres calculated from PET and from PET/CT correlated significantly (r=0.99; p<0.001).
SUVs of cancer lesions and normal organs were comparable between PET and PET/CT, supporting the usefulness of PET/CT-derived SUVs for quantification of tumour metabolism.
在正电子发射断层显像/计算机断层扫描(PET/CT)中,与单独的PET相比,CT衍生的衰减因子可能会影响肿瘤病变和器官中的标准化摄取值(SUV)。因此,我们在个体内比较了PET/CT衍生的SUV与单独PET衍生的SUV在各种器官和肿瘤病变中的情况。
前瞻性纳入35例已知或疑似癌症患者。16例患者使用ECAT HR+扫描仪进行了FDG PET扫描,随后使用Biograph Sensation 16 PET/CT扫描仪进行了第二次扫描。19例患者按相反顺序进行扫描。所有图像均采用迭代算法(有序子集期望最大化算法,OSEM)重建。将疑似病变分为膈旁病变和远离膈肌的病变。还计算了脑、肺、肝、脾和椎骨的平均和最大SUV。确定了两个数据集中用于发射数据校正(骨、软组织、肺)的衰减系数(μ值)。使用与患者相同的方案测量了一个包含六个热球和一个冷圆柱体的体模。
共识别出46个病变。对于14个膈旁病变,PET和PET/CT衍生的最大和平均SUV之间存在显著相关性(r分别为0.97;p均<0.001),对于32个远离膈肌的病变,相关性分别为r=0.87和r=0.89;p均<0.001)。在病变或器官中,PET和PET/CT计算的SUV之间未观察到显著差异。在体模中,PET和PET/CT计算的球体内放射性浓度显著相关(r=0.99;p<0.001)。
PET和PET/CT之间癌症病变和正常器官的SUV具有可比性,支持PET/CT衍生的SUV用于肿瘤代谢定量的有效性。