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JOURNAL ARTICLE
META-ANALYSIS
RESEARCH SUPPORT, NON-U.S. GOV'T
REVIEW
Increasing feasibility and utility of (18)F-FDOPA PET for the management of glioma.
Nuclear Medicine and Biology 2015 October
INTRODUCTION: Despite radical treatment therapies, glioma continues to carry with it a uniformly poor prognosis. Patients diagnosed with WHO Grade IV glioma (glioblastomas; GBM) generally succumb within two years, even those with WHO Grade III anaplastic gliomas and WHO Grade II gliomas carry prognoses of 2-5 and 2 years, respectively. PET imaging with (18)F-FDOPA allows in vivo assessment of the metabolism of glioma relative to surrounding tissues. The high sensitivity of (18)F-DOPA imaging grants utility for a number of clinical applications.
METHODS: A collection of published work about (18)F-FDOPA PET was made and a critical review was discussed and written.
RESULTS: A number of research papers have been published demonstrating that in conjunction with MRI, (18)F-FDOPA PET provides greater sensitivity and specificity than these modalities in detection, grading, prognosis and validation of treatment success in both primary and recurrent gliomas. In further comparisons with (11)C-MET, (18)F-FLT, (18)F-FET and MRI, (18)F-FDOPA has shown similar or better efficacy. Recently synthesis cassettes have become available, making (18)F-FDOPA more accessible.
CONCLUSIONS: According to the available data, (18)F-FDOPA PET is a viable radiotracer for imaging and treatment planning of gliomas.
ADVANCES IN KNOWLEDGE AND IMPLICATION FOR PATIENT CARE: (18)F-FDOPA PET appears to be a viable radiopharmaceutical for the diagnosis and treatment planning of gliomas cases, improving on that of MRI and (18)F-FDG PET.
METHODS: A collection of published work about (18)F-FDOPA PET was made and a critical review was discussed and written.
RESULTS: A number of research papers have been published demonstrating that in conjunction with MRI, (18)F-FDOPA PET provides greater sensitivity and specificity than these modalities in detection, grading, prognosis and validation of treatment success in both primary and recurrent gliomas. In further comparisons with (11)C-MET, (18)F-FLT, (18)F-FET and MRI, (18)F-FDOPA has shown similar or better efficacy. Recently synthesis cassettes have become available, making (18)F-FDOPA more accessible.
CONCLUSIONS: According to the available data, (18)F-FDOPA PET is a viable radiotracer for imaging and treatment planning of gliomas.
ADVANCES IN KNOWLEDGE AND IMPLICATION FOR PATIENT CARE: (18)F-FDOPA PET appears to be a viable radiopharmaceutical for the diagnosis and treatment planning of gliomas cases, improving on that of MRI and (18)F-FDG PET.
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