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Published online before print July 24, 2007, 10.1148/radiol.2443061063
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(Radiology 2007;244:797-806.)
© RSNA, 2007


Genitourinary Imaging

Prostate Cancer: Sextant Localization with MR Imaging, MR Spectroscopy, and 11C-Choline PET/CT1

Claudia Testa, PhD, Riccardo Schiavina, MD, Raffaele Lodi, MD, Eugenio Salizzoni, MD, Barbara Corti, MD, Mohsen Farsad, MD, John Kurhanewicz, PhD, Fabio Manferrari, MD, Eugenio Brunocilla, MD, Caterina Tonon, MD, Nino Monetti, MD, Paolo Castellucci, MD, Stefano Fanti, MD, Manuela Coe, MD, Walter F. Grigioni, MD, Giuseppe Martorana, MD, Romeo Canini, MD, and Bruno Barbiroli, MD

1 From the Department of Clinical Medicine and Applied Biotechnology "D. Campanacci" (C. Testa, R.L., C. Tonon, B.B.), Department of Urology (R.S., F.M., E.B., G.M.), Clinical Department of Radiologic and Histopathologic Science, Diagnostic Imaging Section "V. Bollini" (E.S., M.C., R.C.), Pathologic Anatomy Unit, Institute of Oncology "F. Addarii" (B.C., W.F.G.), and Department of Nuclear Medicine, P.E.T. Center (M.F., N.M., P.C., S.F.), Policlinico S. Orsola-Malpighi, University of Bologna, Via Massarenti 9, 40138 Bologna, Italy; and Department of Radiology, University of California-San Francisco, San Francisco, Calif (J.K.). Received June 19, 2006; revision requested August 21; revision received November 9; accepted December 18; final version accepted January 16, 2007. Address correspondence to R.L. (e-mail: raffaele.lodi{at}unibo.it).

Purpose: To retrospectively compare sensitivity and specificity of magnetic resonance (MR) imaging, three-dimensional (3D) MR spectroscopy, combined MR imaging and 3D MR spectroscopy, and carbon 11 (11C)-choline positron emission tomography (PET)/computed tomography (CT) for intraprostatic tumor sextant localization, with histologic findings as reference standard.

Materials and Methods: The local ethics committee on human research provided approval and a waiver of informed consent for the retrospective study. MR imaging, 3D MR spectroscopy, and 11C-choline PET/CT results were retrospectively reviewed in 26 men with biopsy-proved prostate cancer (mean age, 64 years; range, 51–75 years) who underwent radical prostatectomy. Cancer was identified as areas of nodular low signal intensity on T2-weighted MR images. At 3D MR spectroscopy, choline-plus-creatine–to–citrate and choline-to-creatine ratios were used to distinguish healthy from malignant voxels. At PET/CT, focal uptake was visually assessed, and maximum standardized uptake values (SUVs) were recorded. Agreement between 3D MR spectroscopic and PET/CT results was calculated, and ability of maximum SUV to help localize cancer was assessed with receiver operating characteristic analysis. Significant differences between positive and negative sextants with respect to mean maximum SUV were calculated with a paired t test.

Results: Sensitivity, specificity, and accuracy were, respectively, 55%, 86%, and 67% at PET/CT; 54%, 75%, and 61% at MR imaging; and 81%, 67%, and 76% at 3D MR spectroscopy. The highest sensitivity was obtained when either 3D MR spectroscopic or MR imaging results were positive (88%) at the expense of specificity (53%), while the highest specificity was obtained when results with both techniques were positive (90%) at the expense of sensitivity (48%). Concordance between 3D MR spectroscopic and PET/CT findings was slight ({kappa} = 0.139).

Conclusion: In localizing cancer within the prostate, comparable specificity was obtained with either 3D MR spectroscopy and MR imaging or PET/CT; however, PET/CT had lower sensitivity relative to 3D MR spectroscopy alone or combined with MR imaging.

© RSNA, 2007




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