Molecular Imaging Assessment of Androgen Deprivation Therapy in Prostate Cancer

被引:3
|
作者
Jadvar, Hossein [1 ,2 ,3 ]
Colletti, Patrick M. [1 ]
机构
[1] Univ Southern Calif, USC Keck Sch Med, Dept Radiol, Div Nucl Med, Los Angeles, CA USA
[2] Univ Southern Calif, Kenneth Norris Jr Comprehens Canc Ctr, Los Angeles, CA USA
[3] 2250 Alcazar St,CSC 102, Los Angeles, CA 90033 USA
基金
美国国家卫生研究院;
关键词
Prostate; Hormone; Androgen; Imaging; Choline; Fluciclovine; PSMA; FDG; EMISSION TOMOGRAPHY/COMPUTED TOMOGRAPHY; F-18-CHOLINE PET/CT; MEMBRANE ANTIGEN; CASTRATION-RESISTANT; TRACER UPTAKE; EXPRESSION; RECEPTOR; C-11-CHOLINE; F-18-FDG; RECURRENCE;
D O I
10.1016/j.cpet.2022.02.003
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
centered over various methods of androgen signaling blockade. In this clinical setting, then it is important to understand how androgens and ADT affect the tumor uptake of new-generation imaging agents. ADT typically decreases the uptake of metabolic tracers such as FDG, radiolabeled choline, and fluciclovine, whereas the effect on the expression of transmembrane proteins such as PSMA is more complex and may depend on the tumor biology and the time of imaging after the start of ADT. Additional prospective studies are needed to understand this dynamic behavior and how it may be leveraged optimally for imaging and for radioligand therapy.
引用
收藏
页码:389 / 397
页数:9
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