PET Imaging in Prostate Cancer: Focus on Prostate-Specific Membrane Antigen

被引:144
作者
Mease, Ronnie C. [1 ]
Foss, Catherine A. [1 ]
Pomper, Martin G. [1 ]
机构
[1] Johns Hopkins Med Sch, Russell H Morgan Dept Radiol & Radiol Sci, Baltimore, MD 21287 USA
关键词
DCFBC; molecular imaging; positron emission tomography; PSMA; radiopharmaceutical; POSITRON-EMISSION-TOMOGRAPHY; GLUTAMATE-CARBOXYPEPTIDASE-II; UREA-BASED INHIBITORS; BAY; 1075553; PET/CT; RADIATION-DOSIMETRY; PSMA EXPRESSION; PHASE-I; ANTI-1-AMINO-3-F-18-FLUOROCYCLOBUTANE-1-CARBOXYLIC ACID; PRECLINICAL EVALUATION; MONOCLONAL-ANTIBODY;
D O I
10.2174/1568026611313080008
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Prostate cancer (PCa) is the second leading cause of cancer-related death in American men. Positron emission tomography/computed tomography (PET/CT) with emerging radiopharmaceuticals promises accurate staging of primary disease, restaging of recurrent disease, detection of metastatic lesions and, ultimately, for predicting the aggressiveness of disease. Prostate-specific membrane antigen (PSMA) is a well-characterized imaging biomarker of PCa. Because PSMA levels are directly related to androgen independence, metastasis and progression, PSMA could prove an important target for the development of new radiopharmaceuticals for PET. Preclinical data for new PSMA-based radiotracers are discussed and include new Zr-89- and Cu-64-labeled anti-PSMA antibodies and antibody fragments, Cu-64-labeled aptamers, and C-11-, F-18-, Ga-68-, Cu-64-, and Y-86-labeled low molecular weight inhibitors of PSMA. Several of these agents, namely Ga-68-HBED-CC conjugate 15, F-18-DCFBC 8, and BAY1075553 are particularly promising, each having detected sites of PCa in initial clinical studies. These early clinical results suggest that PET/CT using PSMA-targeted agents, especially with compounds of low molecular weight, will make valuable contributions to the management of PCa.
引用
收藏
页码:951 / 962
页数:12
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