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Current Molecular Imaging Positron Emitting Radiotracers in Oncology

期刊

NUCLEAR MEDICINE AND MOLECULAR IMAGING
卷 45, 期 1, 页码 1-14

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s13139-011-0075-y

关键词

Molecular imaging; Oncologic tracer; PET

资金

  1. NIH [P50 CA 128301-0002]

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Molecular imaging is one of the fastest growing areas of medical imaging. Positron emission tomography (PET) has been widely used in the clinical management of patients with cancer. Nuclear imaging provides biological information at the cellular, subcellular, and molecular level in living subjects with noninvasive procedures. In particular, PET imaging takes advantage of traditional diagnostic imaging techniques and introduces positron-emitting probes to determine the expression of indicative molecular targets at different stages of cancer. F-18-fluorodeoxyglucose (F-18-FDG), the only FDA approved oncological PET tracer, has been widely utilized in cancer diagnosis, staging, restaging, and even monitoring response to therapy; however, F-18-FDG is not a tumor-specific PET tracer. Over the last decade, many promising tumor-specific PET tracers have been developed and evaluated in preclinical and clinical studies. This review provides an overview of the current non-(18)FFDG PET tracers in oncology that have been developed based on tumor characteristics such as increased metabolism, hyperproliferation, angiogenesis, hypoxia, apoptosis, and tumor-specific antigens and surface receptors.

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