TY - JOUR
T1 - 18F-FLT and 18F-FDG positron emission tomography for the imaging of advanced well-differentiated gastro-entero-pancreatic endocrine tumours
AU - Giammarile, Francesco
AU - Billotey, Claire
AU - Lombard-Bohas, Catherine
AU - Le Bars, Didier
AU - Bournaud, Claire
AU - Masson, Sandrine
AU - Walter, Thomas
AU - Houzard, Claire
AU - Scoazec, Jean Yves
AU - Hervieu, Valérie
AU - Vuillez, Jean Philippe
AU - Cornu, Catherine
AU - Janier, Marc
AU - Borson-Chazot, Françoise
PY - 2011/2/1
Y1 - 2011/2/1
N2 - Purpose: Gastro-entero-pancreatic (GEP) endocrine tumours are a heterogenous group of tumours of variable localization and prognosis. It has been suggested that positron emission tomography (PET) using 2-[F]fluoro-2-deoxy-D-glucose (F-FDG) may have a prognostic value and help to identify patients at risk of progression. [F]fluoro-3′-deoxy-3′-L- fluorothymidine (F-FLT) has been recently developed as a PET proliferation tracer. At present, there are no studies investigating its role in GEP. The aim of this prospective study was to assess the value of F-FLT-PET for the evaluation of GEP. Materials and methods: Ten patients with biopsy-proven locally advanced or metastasized, well-differentiated GEP neuroendocrine tumours were prospectively enroled and scheduled for F-FDG and F-FLT-PET. Images were compared with other conventional diagnostic procedures, namely computed tomography, ultrasound, somatostatin receptor scintigraphy and with clinical and diagnostic follow-up. Results: Evaluation criteria were interpreted in terms of assumed presence of tumoral tissue. According to the patients status, FDG was positive in five out of the seven patients with stable disease and in two out of the three patients with progressive disease. No positive case was identified by F-FLT in either the primary or the metastatic tumour site, whatever the status of patients, and this was probably a reflection of the slow proliferation rate of tumours. Conclusions: These preliminary data suggest that F-FLT-PET is not a suitable tracer for the evaluation of advanced well-differentiated GEP tumours. FDG showed good diagnostic performance but does not help to identify patients at risk of progression.
AB - Purpose: Gastro-entero-pancreatic (GEP) endocrine tumours are a heterogenous group of tumours of variable localization and prognosis. It has been suggested that positron emission tomography (PET) using 2-[F]fluoro-2-deoxy-D-glucose (F-FDG) may have a prognostic value and help to identify patients at risk of progression. [F]fluoro-3′-deoxy-3′-L- fluorothymidine (F-FLT) has been recently developed as a PET proliferation tracer. At present, there are no studies investigating its role in GEP. The aim of this prospective study was to assess the value of F-FLT-PET for the evaluation of GEP. Materials and methods: Ten patients with biopsy-proven locally advanced or metastasized, well-differentiated GEP neuroendocrine tumours were prospectively enroled and scheduled for F-FDG and F-FLT-PET. Images were compared with other conventional diagnostic procedures, namely computed tomography, ultrasound, somatostatin receptor scintigraphy and with clinical and diagnostic follow-up. Results: Evaluation criteria were interpreted in terms of assumed presence of tumoral tissue. According to the patients status, FDG was positive in five out of the seven patients with stable disease and in two out of the three patients with progressive disease. No positive case was identified by F-FLT in either the primary or the metastatic tumour site, whatever the status of patients, and this was probably a reflection of the slow proliferation rate of tumours. Conclusions: These preliminary data suggest that F-FLT-PET is not a suitable tracer for the evaluation of advanced well-differentiated GEP tumours. FDG showed good diagnostic performance but does not help to identify patients at risk of progression.
KW - endocrine tumour
KW - fluorodeoxyglucose
KW - fluorothymidine
KW - positron emission tomography imaging
UR - http://www.scopus.com/inward/record.url?scp=78650929396&partnerID=8YFLogxK
U2 - 10.1097/MNM.0b013e3283412143
DO - 10.1097/MNM.0b013e3283412143
M3 - Article
C2 - 21076344
AN - SCOPUS:78650929396
SN - 0143-3636
VL - 32
SP - 91
EP - 97
JO - Nuclear Medicine Communications
JF - Nuclear Medicine Communications
IS - 2
ER -