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Continuing Education |
1 Department of Radiation Oncology and Molecular Radiation Sciences, Johns Hopkins University, Baltimore, Maryland; 2 Department of Medical Physics, Memorial Sloan-Kettering Cancer Center, New York, New York; and 3 Russell H. Morgan Department of Radiology and Radiological Sciences, Johns Hopkins University, Baltimore, Maryland
Correspondence: For correspondence or reprints contact: Eric C. Ford, Department of Radiation Oncology and Molecular Radiation Sciences, Johns Hopkins University, 401 N. Broadway, Suite 1440, Baltimore, MD 21231. E-mail: eric.ford{at}jhmi.edu
Advances in technology have allowed extremely precise control of radiation dose delivery and localization within a patient. The ability to confidently delineate target tumor boundaries, however, has lagged behind. 18F-FDG PET/CT, with its ability to distinguish metabolically active disease from normal tissue, may provide a partial solution to this problem. Here we review the current applications of 18F-FDG PET/CT in a variety of disease sites, including non–small cell lung cancer, head and neck cancer, and pancreatic adenocarcinoma. This review focuses on the use of 18F-FDG PET/CT to aid in planning radiotherapy and the associated benefits and challenges. We also briefly consider novel radiopharmaceuticals that are beginning to be used in the context of radiotherapy planning.
Key Words: radiation therapy IMRT IGRT FDG (fluorodeoxyglucose) FDG PET/CT
* NOTE: FOR CE CREDIT, YOU CAN ACCESS THIS ACTIVITY THROUGH THE SNM WEB SITE (http://www.snm.org/ce_online) THROUGH OCTOBER 2010.
No potential conflict of interest relevant to this article was reported.
COPYRIGHT © 2009 by the Society of Nuclear Medicine, Inc.
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