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Journal of Nuclear Medicine Vol. 46 No. 10 1642-1649
© 2005 by Society of Nuclear Medicine


Clinical Investigations

Detection and Localization of Prostate Cancer: Correlation of 11C-Choline PET/CT with Histopathologic Step-Section Analysis

Mohsen Farsad, MD1, Riccardo Schiavina, MD2, Paolo Castellucci, MD1, Cristina Nanni, MD1, Barbara Corti, MD3, Giuseppe Martorana, MD2, Romeo Canini, MD4, Walter Grigioni, MD3, Stefano Boschi, ScD1, Mario Marengo, ScD1, Cinzia Pettinato, ScD1, Eugenio Salizzoni, MD4, Nino Monetti, MD1, Roberto Franchi, MD1 and Stefano Fanti, MD1

1 Nuclear Medicine Department, PET Unit, Policlinico S. Orsola-Malpighi, Bologna, Italy
2 Urology Department, Università di Bologna, Bologna, Italy
3 Pathology Department, Università di Bologna, Bologna, Italy
4 Radiology Department, Università di Bologna, Bologna, Italy

This study evaluated the potential usefulness of 11C-choline PET/CT for detection and localization of tumors within the prostate. We used the results of step-section histopathologic examination as the standard of reference. Methods: The results were analyzed on a sextant basis. We reviewed the results of the 11C-choline PET/CT scans of 36 patients with prostate cancer and of 5 control subjects with bladder cancer. All patients underwent 11C-choline PET/CT and, subsequently, radical prostatectomy with lymph node dissection within 1 mo. 11C-Choline PET/CT scans were obtained 5–10 min after intravenous injection of 370–555 MBq of 11C-choline. Images were reviewed visually and semiquantitatively using maximum SUV and tumor-to-background ratio. Results: On a sextant basis, histopathologic analysis detected cancer foci in 143 of 216 sextants; high-grade prostate intraepithelial neoplasm foci were detected in 89 of 216 sextants (in 59 sextants in association with carcinoma, in 30 sextants alone), acute prostatitis was detected in 7 of 216 sextants (in 3 sextants in association with carcinoma, in 4 sextants alone), and 39 of 216 sextants were normal. PET/CT demonstrated focal 11C-choline uptake in 108 sextants (94 of which involved tumor), and 108 sextants showed no abnormal 11C-choline uptake (49 of which were false negative). The sensitivity, specificity, accuracy, positive predictive value, and negative predictive value of PET/CT were 66%, 81%, 71%, 87%, and 55%, respectively. In the 5 control subjects, high-grade prostate intraepithelial neoplasm was detected at histologic examination in 16 of 30 sextants. PET/CT showed increased 11C-choline uptake in 5 of 16 sextants. Conclusion: This study demonstrated the feasibility of using 11C-choline PET/CT to identify cancer foci within the prostate. However, we also found that 11C-choline PET/CT has a relative high rate of false-negative results on a sextant basis and that prostatic disorders other than cancer may accumulate 11C-choline. Therefore, our data do not support the routine use of PET/CT with 11C-choline as a first-line screening procedure for prostate cancer in men at high risk.

Key Words: 11C-choline PET/CT • prostate cancer • tumor localization • radionuclide imaging


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