18F-fluoromethylcholine (FCH) PET imaging in patients with castration-resistant prostate cancer: prospective comparison with standard imaging
Creators
- 1. WA PET Service, Sir Charles Gairdner Hospital, Perth, WA (Australia)
- 2. Royal Perth Hospital, Department of Nuclear Medicine, Perth, WA (Australia)
- 3. Royal Perth Hospital, Department of Medical Engineering and Physics, Perth, WA (Australia)
- 4. University of Western Australia, Faculty of Medicine and Pharmacology, School of Medicine, Perth (Australia)
- 5. Sir Charles Gairdner Hospital, Department of Radiation Oncology, Perth, WA (Australia)
- 6. Royal Perth Hospital, School of Surgery, UWA, Perth (Australia)
- 7. Sir Charles Gairdner Hospital, Department of Medical Technology and Physics, Perth, WA (Australia)
Description
The aim of the study was to assess the utility of 18F-fluorocholine (FCH), compared to standard imaging of bone scan (BS) and contrast-enhanced abdominopelvic computed tomography (CT), in patients with castration-resistant prostate carcinoma. FCH has shown promise as a metabolic imaging agent for prostate carcinoma. Twenty-six patients with castration-resistant prostate carcinoma had FCH, BS and CT imaging within a 2-month period. Individual FCH-positive lesions in bone were compared to the BS and soft tissue lesions were compared to CT. The lesions were then classified as concordant or discordant for the presence or absence of prostate cancer metastases. Discordant bone or soft tissue lesions were followed up with BS or CT, respectively, at 6-month intervals for up to 2 years or until a definitive diagnosis of the discordant lesion could be made. In 13 (50%) of the patients, all lesions identified were concordant; this included 5 patients in whom no lesions could be identified with any imaging modality. In 21 patients, 183 lesions were observed with 149 being concordant and 34 (19%) being discordant (13 patients). Based on follow-up, FCH correctly identified the presence or absence of disease in 27 of 34 lesions, and in 14 cases FCH-positive lesions, not identified on initial imaging, were confirmed as disease on follow-up. The sensitivity, specificity, accuracy, positive predictive and negative predictive values for lesion detection by FCH are 96% (92-98%), 96% (81-99%), 96% (93-97%), 99% (96-100%) and 81% (64-88%), respectively, with 95% confidence intervals shown in parentheses. In this patient cohort, FCH shows good initial concordance (81%) with BS and CT in the detection of metastatic prostate carcinoma. Follow-up of the cases where FCH was initially discordant with subsequent BS or CT shows that FCH was accurate in determining the presence or absence of prostate metastasis in 79% of lesions. While FCH imaging as compared to BS and CT in this patient group has a good sensitivity and specificity for the detection of lesions representing prostate metastasis, further prospective studies are needed to determine its role. (orig.)
Availability note (English)
Available from: http://dx.doi.org/10.1007/s00259-010-1579-xAdditional details
Identifiers
Publishing Information
- Journal Title
- European Journal of Nuclear Medicine and Molecular Imaging
- Journal Volume
- 38
- Journal Issue
- 1
- Journal Page Range
- p. 14-22
- ISSN
- 1619-7070
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 43006937
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- ABDOMEN; CARCINOMAS; CASTRATION; CHOLINE; CONTRAST MEDIA; FLUORINE 18; HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY; METABOLISM; METASTASES; ORGANIC FLUORINE COMPOUNDS; PELVIS; POSITRON COMPUTED TOMOGRAPHY; PROSTATE; RADIOPHARMACEUTICALS; SCINTISCANNING; SENSITIVITY; SKELETON; WHOLE-BODY COUNTING
- Descriptors DEC
- ALCOHOLS; AMMONIUM COMPOUNDS; BETA DECAY RADIOISOTOPES; BETA-PLUS DECAY RADIOISOTOPES; BODY; CHROMATOGRAPHY; COMPUTERIZED TOMOGRAPHY; COUNTING TECHNIQUES; DIAGNOSTIC TECHNIQUES; DISEASES; DRUGS; EMISSION COMPUTED TOMOGRAPHY; FLUORINE ISOTOPES; GLANDS; HOURS LIVING RADIOISOTOPES; HYDROXY COMPOUNDS; ISOMERIC TRANSITION ISOTOPES; ISOTOPES; LABELLED COMPOUNDS; LIGHT NUCLEI; LIPOTROPIC FACTORS; LIQUID COLUMN CHROMATOGRAPHY; MALE GENITALS; MATERIALS; MEDICINE; NANOSECONDS LIVING RADIOISOTOPES; NEOPLASMS; NUCLEI; ODD-ODD NUCLEI; ORGANIC COMPOUNDS; ORGANIC HALOGEN COMPOUNDS; ORGANS; QUATERNARY AMMONIUM COMPOUNDS; RADIOACTIVE MATERIALS; RADIOISOTOPE SCANNING; RADIOISOTOPES; SEPARATION PROCESSES; SURGERY; TOMOGRAPHY