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Year:
2012
| Volume: 20
| Issue: 3-4
| Pages: 84-85
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Special Article |
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IS THERE THE ROLE OF 18F-CHOLINE PET/CT IN PROSTATE CANCER PATIENTS?
Marina Hodolic |
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DOI:
10.2298/AOO1204084H |
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Abstract: |
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Prostate cancer is the ninth-most-common cancer in the world and the most common life-threatening cancer affecting men in the western countries. More than 80% of men will develop prostate cancer by the age of 80. Physiologically, choline is a component of cell membranes. It presents a high affinity for malignant prostate tissue. Choline, labeled with 11C or 18F is the essential part of most sensitive nuclear medicine procedure for imaging of spread of prostate cancer today. 11C-choline is preferred due to lower urinary excretion and patient exposure. Due to shorter half-life time of 11C (20 minutes), 18F-choline (half-life time of 110 minutes) is more useful for possible distribution to centers lacking on-site cyclotron. The sensitivity of 18F-choline PET/CT to detect prostate cancer preoperatively is 73%, greater than with 18F-FDG PET/CT (31%). Also, the accuracy is greater with 18F-choline PET/CT (67%) than using 18F-FDG PET/CT (53%). The major goal of pretherapeutic imaging with 18F-choline PET/CT is detection of loco-regional and distant metastases. The exact pretherapeutic diagnosis and staging are mandatory, because the tumor treatment must be selected in strict dependence on the clinical tumor stage and risk profile. In patients with biochemical relapse after the radical prostatectomy or radiotherapy of prostate cancer, 18F-choline PET/CT represents a noninvasive, whole body study that allows disease localization. Detection sensitivity is negatively correlated with serum PSA concentration (ng/ml) and positively correlated with Gleason score. 18F-choline PET/CT is becoming the essential imaging modality in patients with prostate cancer to demonstrate spread of the disease preoperatively and to detect local and distant recurrent disease after radical prostatectomy or radiotherapy. |
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Key words:
Prostatic Neoplasms; Positron-Emission Tomography and Computed Tomography; Choline; Diagnostic Imaging; Neoplasm Recurrence, Local; Prostate-Specific Antigen |
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