TY - JOUR
T1 - Postoperative fluorine-18-fluorodeoxyglucose positron emission tomography/computed tomography
T2 - An important imaging modality in patients with aggressive histology of differentiated thyroid cancer
AU - Nascimento, Camila
AU - Borget, Isabelle
AU - Al Ghuzlan, Abir
AU - Deandreis, Désirée
AU - Hartl, Dana
AU - Lumbroso, Jean
AU - Berdelou, Amandine
AU - Lepoutre-Lussey, Charlotte
AU - Mirghani, Haïtham
AU - Baudin, Eric
AU - Schlumberger, Martin
AU - Leboulleux, Sophie
N1 - Publisher Copyright:
© 2015 Mary Ann Liebert, Inc.
PY - 2015/4/1
Y1 - 2015/4/1
N2 - Background: Aggressive histopathologic subtypes of differentiated thyroid cancer (DTC) are fluorodeoxyglucose (FDG)-avid tumors and are at high risk for persistent/recurrent disease. In these patients, fluorodeoxyglucose positron emission tomography/computed tomography (FDG-PET/CT) is performed in cases of suspicion of recurrence based on thyroglobulin (Tg) levels or thyroglobulin antibodies (TgAb). The goals of this study were to evaluate the sensitivity of systematic postoperative FDG-PET/CT and to identify risk factors for abnormal FDG-PET/CT. Methods: Single-center retrospective study of 38 consecutive patients (16 males, 22 females; mean age, 57 years) with aggressive histology DTC, without known persistent disease at the time of postoperative radioactive iodine (RAI) ablation. The most frequent aggressive histologic subtypes were tall cell papillary carcinoma (45%) and poorly differentiated carcinoma (42%). Results: A total of 86 lesions were found in 20 (53%) patients, distributed in 33 organs. FDG-PET/CT and the postablation whole-body scan (RAI WBS) showed persistent disease in 15 and 12 patients, respectively. FDG-PET/CT was more sensitive than WBS for the detection of individual lesions (69% vs. 59%). Both imaging techniques were complementary with 41% of the lesions detected only by FDG-PET/CT and 31% only by RAI WBS. The only risk factor of abnormal FDG-PET/CT was a stimulated Tg level (Tg/TSH) measured at ablation >10 ng/mL with persistent disease showing FDG uptake in 72% of the patients with a Tg/TSH >10 ng/mL and in 10% of the patients with Tg/TSH ≤10 ng/mL. Conclusion: Postoperative FDG-PET/CT should be performed routinely in patients with aggressive histology DTC.
AB - Background: Aggressive histopathologic subtypes of differentiated thyroid cancer (DTC) are fluorodeoxyglucose (FDG)-avid tumors and are at high risk for persistent/recurrent disease. In these patients, fluorodeoxyglucose positron emission tomography/computed tomography (FDG-PET/CT) is performed in cases of suspicion of recurrence based on thyroglobulin (Tg) levels or thyroglobulin antibodies (TgAb). The goals of this study were to evaluate the sensitivity of systematic postoperative FDG-PET/CT and to identify risk factors for abnormal FDG-PET/CT. Methods: Single-center retrospective study of 38 consecutive patients (16 males, 22 females; mean age, 57 years) with aggressive histology DTC, without known persistent disease at the time of postoperative radioactive iodine (RAI) ablation. The most frequent aggressive histologic subtypes were tall cell papillary carcinoma (45%) and poorly differentiated carcinoma (42%). Results: A total of 86 lesions were found in 20 (53%) patients, distributed in 33 organs. FDG-PET/CT and the postablation whole-body scan (RAI WBS) showed persistent disease in 15 and 12 patients, respectively. FDG-PET/CT was more sensitive than WBS for the detection of individual lesions (69% vs. 59%). Both imaging techniques were complementary with 41% of the lesions detected only by FDG-PET/CT and 31% only by RAI WBS. The only risk factor of abnormal FDG-PET/CT was a stimulated Tg level (Tg/TSH) measured at ablation >10 ng/mL with persistent disease showing FDG uptake in 72% of the patients with a Tg/TSH >10 ng/mL and in 10% of the patients with Tg/TSH ≤10 ng/mL. Conclusion: Postoperative FDG-PET/CT should be performed routinely in patients with aggressive histology DTC.
UR - http://www.scopus.com/inward/record.url?scp=84926505727&partnerID=8YFLogxK
U2 - 10.1089/thy.2014.0320
DO - 10.1089/thy.2014.0320
M3 - Article
C2 - 25633259
AN - SCOPUS:84926505727
SN - 1050-7256
VL - 25
SP - 437
EP - 444
JO - Thyroid
JF - Thyroid
IS - 4
ER -