Radiotherapy & Oncology
Volume 96, Issue 3 , Pages 280-287, September 2010

PET radiopharmaceuticals in radiation treatment planning – Synthesis and biological characteristics

  • Roland Haubner

      Affiliations

    • Corresponding Author InformationAddress: Medizinische Universität Innsbruck, Anichstr. 35, Innsbruck, Austria.

Medizinische Universität Innsbruck, Innsbruck, Austria

Received 23 July 2010; received in revised form 29 July 2010; accepted 29 July 2010. published online 19 August 2010.

Abstract 

During the last decade several different PET radiopharmaceuticals entered into the clinic and positron emission tomography (PET) became an important tool for staging of cancer patients and assessing response to therapy. Meanwhile FDG-PET has also found application in radiation treatment planning. Potential radiopharmaceuticals for radiation treatment planning may also include tracers allowing monitoring of proliferation, amino acid metabolism, hypoxia, lipid metabolism and receptor expression. Here the syntheses of a selection of clinically tested promising tracers are summarized and the different molecular mechanisms for accumulation are discussed which may help to choose the appropriate tracer for planning radiation treatment strategies.

Keywords: Glucose metabolism, Amino acid metabolism, Hypoxia, Proliferation, Lipid metabolism, Angiogenesis, SSTR expression

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PII: S0167-8140(10)00449-4

doi:10.1016/j.radonc.2010.07.022

Radiotherapy & Oncology
Volume 96, Issue 3 , Pages 280-287, September 2010