Differential Background Clearance of Fluorodeoxyglucose Activity in Normal Tissues and its Clinical Significance

被引:5
作者
Cheng, Gang [1 ,2 ]
Alavi, Abass [2 ]
Lee, Nam Ju [2 ]
Akers, Scott R. [1 ]
机构
[1] Philadelphia VA Med Ctr, Dept Radiol, 3900 Woodland Ave, Philadelphia, PA 19104 USA
[2] Hosp Univ Penn, Dept Radiol, Philadelphia, PA 19104 USA
关键词
Fluorodeoxyglucose; PET; SUV; Distribution time; Background activity; Delayed imaging;
D O I
10.1016/j.cpet.2013.12.001
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
The clearance of 2-deoxy-2-[18F] fluoro-D-glucose (FDG) activity in normal tissues varies significantly with extended distribution time. Although most tissues have lower standardized uptake value (SUV) on 2-hour/3-hour delayed images, others may have stable or higher FDG activity with longer distribution times. The continuously decreased SUV on delayed imaging in some tissues, especially in the liver, indicates that longer distribution time will decrease background activity, increase lesion-to-background ratio, and thus improve imaging quality, whereas the continuously increased SUV from 1 to 3 hours in the heart suggest that longer distribution time will improve detection of viable myocardium in a viability study.
引用
收藏
页码:209 / +
页数:9
相关论文
共 22 条
[1]  
Delbeke D., Coleman R.E., Guiberteau M.J., Et al., Procedure guideline for tumor imaging with 18F-FDG PET/CT 1.0, J Nucl Med, 47, 5, pp. 885-895, (2006)
[2]  
Juweid M.E., Stroobants S., Hoekstra O.S., Et al., Use of positron emission tomography for response assessment of lymphoma: Consensus of the Imaging Subcommittee of International Harmonization Project in Lymphoma, J Clin Oncol, 25, 5, pp. 571-578, (2007)
[3]  
Hustinx R., Smith R.J., Benard F., Et al., Dual time point fluorine-18 fluorodeoxyglucose positron emission tomography: A potential method to differentiate malignancy from inflammation and normal tissue in the head and neck, Eur J Nucl Med, 26, 10, pp. 1345-1348, (1999)
[4]  
Zhuang H., Pourdehnad M., Lambright E.S., Et al., Dual time point 18F-FDG PET imaging for differentiating malignant from inflammatory processes, J Nucl Med, 42, 9, pp. 1412-1417, (2001)
[5]  
Matthies A., Hickeson M., Cuchiara A., Et al., Dual time point 18F-FDG PET for the evaluation of pulmonary nodules, J Nucl Med, 43, 7, pp. 871-875, (2002)
[6]  
Alkhawaldeh K., Bural G., Kumar R., Et al., Impact of dual-time-point (18)F-FDG PET imaging and partial volume correction in the assessment of solitary pulmonary nodules, Eur J Nucl Med Mol Imaging, 35, 2, pp. 246-252, (2008)
[7]  
Cheng G., Torigian D.A., Zhuang H., Et al., When should we recommend use of dual time-point and delayed time-point imaging techniques in FDG PET?, Eur J Nucl Med Mol Imaging, 40, 5, pp. 779-787, (2013)
[8]  
Higashi T., Saga T., Nakamoto Y., Et al., Relationship between retention index in dual-phase (18)F-FDG PET, and hexokinase-II and glucose transporter-1 expression in pancreatic cancer, J Nucl Med, 43, 2, pp. 173-180, (2002)
[9]  
Cheng G., Alavi A., Lim E., Et al., Dynamic changes of FDG uptake and clearance in normal tissues, Mol Imaging Biol, 15, 3, pp. 345-352, (2013)
[10]  
Chin B.B., Green E.D., Turkington T.G., Et al., Increasing uptake time in FDG-PET: Standardized uptake values in normal tissues at 1 versus 3 h, Mol Imaging Biol, 11, 2, pp. 118-122, (2009)