Whole-body tumor imaging: O-[11C]methyl-l-tyrosine/positron emission tomography

Kiichi Ishiwata, Kuzuo Kubota, Tadashi Nariai, Ren Iwata

    Research output: Chapter in Book/Report/Conference proceedingChapter

    2 Citations (Scopus)


    This chapter describes the development of O-[11C]methyl-L-tyrosine (OMT) and its first clinical application to whole-body imaging as well as brain tumor imaging. Radiolabeled amino acids such as L-[methyl-11C]methionine (MET) are taken up into normal brain tissue at much lower levels, which enables imaging of the majority of low- and high-grade brain tumors. MET is applied for diagnosing tumors in the chest region as well as the brain, but not in the abdominal region where the natural amino acids are taken up at high levels in organs such as the pancreas and liver. On the other hand, the artificial amino acid O-[18F]fluoroethyl-L-tyrosine is accumulated at very low levels in the human pancreas and liver but excreted from the kidneys to the bladder through the urinary tract. This finding could be characteristically common to artificial amino acid tracers that reflect amino acid transport. Multiple tracers can be administered to the individuals on the same day for a differential diagnosis with OMT-PET followed by FDG-PET. The use of 11C-labeled tracers usually results in decreased radiation absorbed doses compared with the use of 18F-tracers that have longer half-lives. Positron-labeled amino acids have been identified as a suitable imaging probe to evaluate the pathophysiology of brain tumors using PET. Among the various amino acid tracers, MET is used in most clinical studies of brain tumors because of its simple and efficient labeling procedure.

    Original languageEnglish
    Title of host publicationCancer Imaging
    PublisherAcademic Press
    Number of pages5
    ISBN (Print)9780123742124
    Publication statusPublished - 2008

    ASJC Scopus subject areas

    • Radiological and Ultrasound Technology
    • Oncology
    • Radiology Nuclear Medicine and imaging


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