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FDG PET/CT in oncology: “raising the bar”

  • C.N. Patel

      Affiliations

    • Departments of Radiology & Nuclear Medicine, Churchill Hospital, Oxford Radcliffe NHS Trust, Oxford, UK
  • ,
  • A.R. Goldstone

      Affiliations

    • Departments of Radiology & Nuclear Medicine, St James's University Hospital, Leeds Teaching Hospitals NHS Trust, Leeds, UK
  • ,
  • F.U. Chowdhury

      Affiliations

    • Departments of Radiology & Nuclear Medicine, St James's University Hospital, Leeds Teaching Hospitals NHS Trust, Leeds, UK
  • ,
  • A.F. Scarsbrook

      Affiliations

    • Departments of Radiology & Nuclear Medicine, St James's University Hospital, Leeds Teaching Hospitals NHS Trust, Leeds, UK
    • Corresponding Author InformationGuarantor and correspondent: Departments of Radiology and Nuclear Medicine, St James's Institute of Oncology, St James's University Hospital, Beckett Street, Leeds LS9 7TF, UK. Tel.: +44 113 206 8212; fax: +44 113 206 8228.

Received 2 December 2009; received in revised form 23 December 2009; accepted 5 January 2010. published online 14 June 2010.
Corrected Proof

Integrated positron-emission tomography/computed tomography (PET/CT) with 2-[18F]-fluoro-2-deoxy-d-glucose (FDG) has revolutionized oncological imaging in recent years and now has a firmly established role in a variety of tumour types. There have been simultaneous step-wise advances in scanner technology, which are yet to be exploited to their full potential in clinical practice. This article will review these technological developments and explore how refinements in imaging protocols can further improve the accuracy and efficacy of PET/CT in oncology. The promises, and limitations, of emerging oncological applications of FDG PET/CT in radiotherapy planning and therapy response assessment will be explored. Potential future developments, including the use of FDG PET probes in oncological surgery, advanced data analysis techniques, and the prospect of integrated PET/magnetic resonance imaging (PET/MRI) will be highlighted.

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PII: S0009-9260(10)00031-0

doi:10.1016/j.crad.2010.01.003

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