TY - JOUR
T1 - 18 F-fluorocholine for prostate cancer imaging
T2 - A systematic review of the literature
AU - Bauman, G.
AU - Belhocine, T.
AU - Kovacs, M.
AU - Ward, A.
AU - Beheshti, M.
AU - Rachinsky, I.
N1 - Funding Information:
This work supported by the Canadian Institute for Health Research (Grant CTP 87515) and the Centre for Probe Development and Commercialization.
PY - 2012/3/1
Y1 - 2012/3/1
N2 - BACKGROUND: Positron emission tomography (PET or combined PET-computed tomography (PET/CT)) allows the non-invasive interrogation of metabolic processes using radiolabeled probes. Altered choline metabolism has been noted as a characteristic of prostate cancer (PCa), and radiolabeled choline and choline analogs have been investigated as PET/CT imaging agents for prostate cancer; 18 Ffluoromethyl-dimethyl-2-hydroxyethyl-ammonium (18 F-FCH) shows particular promise as a PCa imaging agent given its favorable physical and pharmacokinetic properties.METHODS: We conducted a systematic review of results to date with 18 F-FCH. As the tracer was first described by DeGrado in 2001, we limited our search from January 2001 to August 2011.RESULTS: In all, 37 studies including 1244 patients met the inclusion criteria. Studies included those detailing the radiosynthesis of 18 F-FCH, preclinical and early clinical dosimetry, and biodistribution (n=7); evaluation of local disease (n=6), nodal disease (n=5), bone metastases and castrate-resistant disease (n=7), biochemical recurrence (n=11), radiotherapy planning (n=7) and sources of false-positive studies (n=2); and some studies reported on multiple indications. Potential sources of variations in the studies affecting reported performance included case series size, variation in extent of disease at imaging (including Gleason grade, and PSA), selection of gold standards for comparison and variations in scan technique.CONCLUSIONS: On the basis of the review, we suggest potential scenarios where this metabolic imaging might be considered for further evaluation in clinical trials for guiding PCa management.
AB - BACKGROUND: Positron emission tomography (PET or combined PET-computed tomography (PET/CT)) allows the non-invasive interrogation of metabolic processes using radiolabeled probes. Altered choline metabolism has been noted as a characteristic of prostate cancer (PCa), and radiolabeled choline and choline analogs have been investigated as PET/CT imaging agents for prostate cancer; 18 Ffluoromethyl-dimethyl-2-hydroxyethyl-ammonium (18 F-FCH) shows particular promise as a PCa imaging agent given its favorable physical and pharmacokinetic properties.METHODS: We conducted a systematic review of results to date with 18 F-FCH. As the tracer was first described by DeGrado in 2001, we limited our search from January 2001 to August 2011.RESULTS: In all, 37 studies including 1244 patients met the inclusion criteria. Studies included those detailing the radiosynthesis of 18 F-FCH, preclinical and early clinical dosimetry, and biodistribution (n=7); evaluation of local disease (n=6), nodal disease (n=5), bone metastases and castrate-resistant disease (n=7), biochemical recurrence (n=11), radiotherapy planning (n=7) and sources of false-positive studies (n=2); and some studies reported on multiple indications. Potential sources of variations in the studies affecting reported performance included case series size, variation in extent of disease at imaging (including Gleason grade, and PSA), selection of gold standards for comparison and variations in scan technique.CONCLUSIONS: On the basis of the review, we suggest potential scenarios where this metabolic imaging might be considered for further evaluation in clinical trials for guiding PCa management.
KW - 18F-fluorocholine
KW - PET/CT
KW - clinical applications
KW - recommendations
UR - http://www.scopus.com/inward/record.url?scp=84857046932&partnerID=8YFLogxK
U2 - 10.1038/pcan.2011.35
DO - 10.1038/pcan.2011.35
M3 - Review article
C2 - 21844889
AN - SCOPUS:84857046932
SN - 1365-7852
VL - 15
SP - 45
EP - 55
JO - Prostate Cancer and Prostatic Diseases
JF - Prostate Cancer and Prostatic Diseases
IS - 1
ER -