Diagnostic Performance of 18F-Fluciclovine in Detection of Prostate Cancer Bone Metastases.
Diagnostic Performance of 18F-Fluciclovine in Detection of Prostate Cancer Bone Metastases.
复制标题
DOI:
10.1097/rlu.0000000000002130
复制
发表时间:
2018-07
影响因子:
10.6
通讯作者:
Jadvar H
中科院分区:
文献类型:
--
作者:
Chau A;Gardiner P;Colletti PM;Jadvar H
18F-fluciclovine is a synthetic amino acid radiotracer that has recently been approved in Europe and the United States for positron emission tomography (PET) imaging in men with biochemical recurrence (BCR) of prostate cancer following prior definitive treatment. Accurate identification of the sites of disease in patients presenting with BCR of prostate cancer is important in determining the appropriate treatment. Bone is the most frequent site of metastatic disease in patients with prostate cancer. We conducted a comprehensive review of the available preclinical and clinical data on the diagnostic performance of 18F-fluciclovine PET-computed tomography (PET/CT) in an attempt to draw practical and general conclusions on the utility and limitations of 18F-fluciclovine PET/CT in localization of osseous metastatic disease in prostate cancer. The cumulative preclinical data and results of some retrospective and two prospective clinical studies suggest that 18F-fluciclovine can detect early bone marrow involvement in patients with BCR of prostate cancer and negative prior bone specific imaging findings. 18F-Fluciclovine PET/CT appears to offer useful information for early detection of bone metastases in men with BCR of prostate cancer. Additional investigations will be needed to compare the diagnostic performance of 18F-fluciclovine PET/CT to other standard and novel imaging methods in initial staging, BCR and castrate-resistant phases of disease.