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Meeting Report |
1 Cancer Imaging Program, National Cancer Institute, NIH, Rockville, Maryland; 2 Amgen, Inc., Thousand Oaks, California; 3 University of Minnesota, Minneapolis, Minnesota; 4 University of California San Francisco, San Francisco, California; and 5 The Ohio State University, Columbus, Ohio
Requests for reprints: Guoying Liu, Cancer Imaging Program, National Cancer Institute, 6130 Executive Boulevard, Suite 6000, Bethesda, MD 20892-7412. Phone: 301-496-9531; Fax: 301-480-3507; E-mail: liug{at}mail.nih.gov.
Although dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) and magnetic resonance spectroscopy (MRS) have great potential to provide routine assessment of cancer treatment response, their widespread application has been hampered by a lack of standards for use. Thus, the National Cancer Institute convened a workshop to assess developments and applications of these methods, develop standards for methodology, and engage relevant partners (drug and device industries, researchers, clinicians, and government) to encourage sharing of data and methodologies. Consensus recommendations were reached for DCE-MRI methodologies and the focus for initial multicenter trials of MRS. In this meeting report, we outline the presentations, the topics discussed, the ongoing challenges identified, and the recommendations made by workshop participants for the use of DCE-MRI and 1H MRS in the clinical assessment of antitumor therapies.
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