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   <subfield code="a">The ability of 18F-choline PET/CT to identify local recurrence of prostate cancer</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Laura Evangelista, Marino Cimitan, Marina Hodolič, Tanja Baseric, Jure Fettich, Eugenio Borsatti]</subfield>
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   <subfield code="a">Purpose: To determine when 18F-choline PET/CT can truly identify local recurrence of prostate cancer. Methods: 1031 patients from 3 European centers underwent 18F-choline PET/CT (FCH PET/CT) for recurrent disease; 131 subjects (12.7%) showed a positive FCH uptake in the prostatic gland or prostatic fossa. Median age was 72years (range 48-87years), and the median PSA level at the time of FCH PET/CT scan was 4.41ng/mL (0.22-18.13ng/mL). 45 patients (34.4%) had a Gleason score (GS) &gt;7, and the residual subjects had a GS ≤7. The assessment of true or false-positive FCH PET/CT findings was made by magnetic resonance imaging (n=34) and/or biopsy in 75/131 cases. A χ 2 test and a Z Kolmogorov-Smirnov test were used to assess the correlation between clinical variables (age, PSA, GS, type of therapy) and FCH PET/CT findings. Results: FCH PET/CT resulted truly positive (TP) for recurrent disease in the prostatic gland/fossa in 59/75 patients (79%) and falsely positive (FP) in 16 subjects (21%). The median value of PSA at the time of FCH PET/CT scan was higher in TP as compared to FP, although not statistically significant (4.76 vs. 3.04ng/mL p&gt;0.05). Similarly, median age, GS categories, and the type of therapy were similar between the two groups (p&gt;0.05). However, when matching GS categories and PSA values, we found that the number of patients with TP findings were higher in the case of a PSA &gt;2ng/mL, independently from the GS (ranging between 74% and 92%). Conversely, FP rate ranged between 50% and 65% in patients with a PSA ≤2ng/mL, especially in the case of GS ≤7, whereas FP was around 25% in those with a GS &gt;7 and PSA &gt;2ng/mL. Conclusions: FCH PET/CT has a limited role in evaluation of prostatic gland/fossa recurrence, due to the physiological biodistribution of the radiopharmaceutical agent. However, in 70-90% of patients with a PSA &gt;2ng/mL, independently from GS, a focal FCH uptake is compatible with a true local recurrence.</subfield>
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   <subfield code="a">Springer Science+Business Media New York, 2015</subfield>
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   <subfield code="a">Prostate cancer recurrence</subfield>
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   <subfield code="a">18F-choline PET/CT</subfield>
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   <subfield code="a">True positive</subfield>
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   <subfield code="a">Salvage treatments</subfield>
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   <subfield code="a">Evangelista</subfield>
   <subfield code="D">Laura</subfield>
   <subfield code="u">Radiotherapy and Nuclear Medicine Unit, Veneto Institute of Oncology IOV - IRCCS, Via Gattamelata, 64, 35128, Padua, Italy</subfield>
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   <subfield code="a">Cimitan</subfield>
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   <subfield code="u">Nuclear Medicine Unit, IRCCS National Cancer Institute (CRO), Aviano, PN, Italy</subfield>
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   <subfield code="a">Hodolič</subfield>
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   <subfield code="t">Abdominal Imaging</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
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