18F-Labeled, PSMA-Targeted Radiotracers: Leveraging the Advantages of Radiofluorination for Prostate Cancer Molecular Imaging

被引:128
|
作者
Werner, Rudolf A. [1 ,2 ]
Derlin, Thorsten [1 ]
Lapa, Constantin [3 ]
Sheikbahaei, Sara [2 ]
Higuchi, Takahiro [3 ,4 ]
Giesel, Frederik L. [5 ]
Behr, Spencer [6 ]
Drzezga, Alexander [7 ]
Kimura, Hiroyuki [8 ]
Buck, Andreas K. [3 ]
Bengel, Frank M. [1 ]
Pomper, Martin G. [2 ,9 ,10 ]
Gorin, Michael A. [2 ,9 ,10 ]
Rowe, Steven P. [2 ,9 ,10 ]
机构
[1] Hannover Med Sch, Dept Nucl Med, Carl Neuberg Str 1, D-30625 Hannover, Germany
[2] Johns Hopkins Univ, Sch Med, Russell H Morgan Dept Radiol & Radiol Sci, Baltimore, MD USA
[3] Univ Hosp Wurzburg, Dept Nucl Med, Oberdurrbacherstr 6, D-97080 Wurzburg, Germany
[4] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Okayama, Japan
[5] Univ Hosp Heidelberg, Dept Nucl Med, INF 400, D-69120 Heidelberg, Germany
[6] Univ Calif San Francisco, Dept Radiol & Biomed Imaging, San Francisco, CA 94143 USA
[7] Univ Hosp Cologne, Dept Nucl Med, Cologne, Germany
[8] Kyoto Pharmaceut Univ, Dept Analyt & Bioinorgan Chem, Kyoto, Japan
[9] Johns Hopkins Univ, Sch Med, James Buchanan Brady Urol Inst, Baltimore, MD USA
[10] Johns Hopkins Univ, Sch Med, Dept Urol, Baltimore, MD 21205 USA
来源
THERANOSTICS | 2020年 / 10卷 / 01期
基金
美国国家卫生研究院;
关键词
Radiofluorine; prostate-specific membrane antigen; prostate cancer; 18F; PSMA; PET; 68Ga; theranostics; radioligand therapy; POSITRON-EMISSION-TOMOGRAPHY; MEMBRANE ANTIGEN; F-18-DCFPYL PET/CT; RADIOLIGAND THERAPY; RADIATION-DOSIMETRY; INITIAL EVALUATION; BAY; 1075553; T PET/CT; BIODISTRIBUTION; INHIBITOR;
D O I
10.7150/thno.37894
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Prostate-specific membrane antigen (PSMA)-targeted PET imaging for prostate cancer with Ga-68-labeled compounds has rapidly become adopted as part of routine clinical care in many parts of the world. However, recent years have witnessed the start of a shift from Ga-68- to F-18-labeled PSMA-targeted compounds. The latter imaging agents have several key advantages, which may lay the groundwork for an even more widespread adoption into the clinic. First, facilitated delivery from distant suppliers expands the availability of PET radiopharmaceuticals in smaller hospitals operating a PET center but lacking the patient volume to justify an onsite Ge-68/Ga-68 generator. Thus, such an approach meets the increasing demand for PSMA-targeted PET imaging in areas with lower population density and may even lead to cost-savings compared to in-house production. Moreover, F-18-labeled radiotracers have a higher positron yield and lower positron energy, which in turn decreases image noise, improves contrast resolution, and maximizes the likelihood of detecting subtle lesions. In addition, the longer half-life of 110 min allows for improved delayed imaging protocols and flexibility in study design, which may further increase diagnostic accuracy. Moreover, such compounds can be distributed to sites which are not allowed to produce radiotracers on-site due to regulatory issues or to centers without access to a cyclotron. In light of these advantageous characteristics, F-18-labeled PSMA-targeted PET radiotracers may play an important role in both optimizing this transformative imaging modality and making it widely available. We have aimed to provide a concise overview of emerging F-18-labeled PSMA-targeted radiotracers undergoing active clinical development. Given the wide array of available radiotracers, comparative studies are needed to firmly establish the role of the available F-18-labeled compounds in the field of molecular PCa imaging, preferably in different clinical scenarios.
引用
收藏
页码:1 / 16
页数:16
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