Imaging Analysis of HCC Using 18F-FDG-PET/CT

YK Yusuke Kawamura
MK Masahiro Kobayashi
JS Junichi Shindoh
YK Yuta Kobayashi
KK Kayoko Kasuya
TS Tomoya Sano
SF Shunichiro Fujiyama
TH Tetsuya Hosaka
SS Satoshi Saitoh
HS Hitomi Sezaki
NA Norio Akuta
FS Fumitaka Suzuki
YS Yoshiyuki Suzuki
KI Kenji Ikeda
YA Yasuji Arase
MH Masaji Hashimoto
HK Hiromitsu Kumada
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Within the month prior to the initiation of lenvatinib, 18F-FDG-PET/CT was performed using a dedicated whole-body PET scanner (Biograph mCT Flow40, Siemens Healthcare, Germany). Using SYNAPSE VINCENT v4 (Fujifilm Medical Systems, Japan) software for semiquantitative analysis, the volume of interest (VOI) was drawn along the outline of the tumor, and maximum standardized uptake value (SUV-max) and mean SUV (SUV-mean) in each intra- and extrahepatic target tumor were calculated. Of the lesions measured, that with the highest 18F-FDG up take was selected and used to calculate the TLR. Next, to measure normal liver activity, 3 non-overlapping spherical 1-cm3 VOIs were drawn in the liver (2 in the right lobe and 1 in the left) on the axial PET images, avoiding the HCC areas seen on dynamic CT. The TLR was calculated using the following equation: TLR = SUV-max of the tumor/SUV-mean of the normal liver. Based on previous reports [3, 6, 8], we selected a TLR ≥2 to indicate high malignant potential.

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