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Journal of Nuclear Medicine Vol. 47 No. 8 1249-1254
© 2006 by Society of Nuclear Medicine


Clinical Investigation

Imaging Prostate Cancer with 11C-Choline PET/CT

Sven N. Reske1, Norbert M. Blumstein1, Bernd Neumaier1, Hans-Werner Gottfried2, Frank Finsterbusch1, Darius Kocot1, Peter Möller3, Gerhard Glatting1 and Sven Perner3

1 Department of Nuclear Medicine, University of Ulm, Ulm, Germany; 2 Department of Urology, University of Ulm, Ulm, Germany; and 3 Department of Pathology, University of Ulm, Ulm, Germany

Correspondence: For correspondence or reprints contact: Sven N. Reske, MD, Department of Nuclear Medicine, University of Ulm, Robert-Koch-Straße 8, D-89081 Ulm, Germany. E-mail: sven.reske{at}uniklinik-ulm.de

The ability of 11C-choline and multimodality fusion imaging with integrated PET and contrast-enhanced CT (PET/CT) was investigated to delineate prostate carcinoma (PCa) within the prostate and to differentiate cancer tissue from normal prostate, benign prostate hyperplasia, and focal chronic prostatitis. Methods: All patients with PCa gave written informed consent. Twenty-six patients with clinical stage T1, T2, or T3 and biopsy-proven PCa underwent 11C-choline PET/CT after intravenous injection of 1,112 ± 131 MBq 11C-choline, radical retropubic prostatovesiculectomy, and standardized prostate tissue sampling. Maximal standardized uptake values (SUVs) of 11C-choline within 36 segments of the prostate were determined. PET/CT results were correlated with histopathologic results, prostate-specific antigen (PSA), Gleason score, and pT stage. Results: The SUV of 11C-choline in PCa tissue was 3.5 ± 1.3 (mean ± SD) and significantly higher than that in prostate tissue with benign histopathologic lesions (2.0 ± 0.6; P < 0.001 benign histopathology vs. cancer). Visual and quantitative analyses of segmental 11C-choline uptake of each patient unambiguously located PCa in 26 of 26 patients and 25 of 26 patients, respectively. A threshold SUV of 2.65 yielded an area under the receiver-operating-characteristic (ROC) curve of 0.89 ± 0.01 for correctly locating PCa. The maximal 11C-choline SUV did not correlate significantly with PSA or Gleason score but did correlate with T stage (P = 0.01; Spearman r = 0.49). Conclusion: 11C-Choline PET/CT can accurately detect and locate major areas with PCa and differentiate segments with PCa from those with benign hyperplasia, chronic prostatitis, or normal prostate tissue. The maximal tumoral 11C-choline uptake is related to pT stage.

Key Words: prostate carcinoma • 11C-choline • PET/CT




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