TY - JOUR
T1 - Pretreatment primary tumor SUVmax on 18F-FDG PET/CT images predicts outcomes in patients with salivary gland carcinoma treated with definitive intensity-modulated radiation therapy
AU - Hsieh, Cheng En
AU - Ho, Kung Chu
AU - Hsieh, Chia Hsun
AU - Yen, Tzue-Chen
AU - Liao, Chun Ta
AU - Wang, Hung Ming
AU - Lin, Chien Yu
N1 - Publisher Copyright:
© 2017 Wolters Kluwer Health, Inc. All rights reserved.
PY - 2017/9/1
Y1 - 2017/9/1
N2 - Purpose The aim of this study was to investigate the prognostic significance of 18 F-FDG uptake in salivary gland carcinoma (SGC) patients treated with definitive intensity-modulated radiation therapy (IMRT). Methods We retrospectively examined 46 SGC patients who received pretreatment 18 F-FDG PET/CT and definitive IMRT between 2007 and 2014. Most tumors were located in the minor salivary glands (n = 35 [76%]). Forty-six percent (n = 21) of the participants had unresectable disease. The median radiation dose was 72 Gy. Treatment outcomes were examined in relation to clinicopathologic parameters and pretreatment primary tumor SUVmax on 18 F-FDG PET/CT. Results After a median follow-up of 54 months, the 5-year locoregional progression-free survival (LRPFS), distant metastasis-free survival, progression-free survival (PFS), and overall survival (OS) rates were 77%, 75%, 63%, and 61%, respectively. The median primary tumor SUVmax was 7.4 (range, 2.3-23.6), and the optimal cutoff value that maximized the prognostic significance for 5-year PFS was 7.4 (P = 0.006). Patients with a high SUVmax (≥7.4) had significantly lower 5-year LRPFS (P = 0.007), distant metastasis-free survival (P = 0.046), and OS (P = 0.013) rates than those with a low SUVmax (<7.4). Multivariate analyses identified SUVmax as the only independent predictor of LRPFS (P = 0.023) and PFS (P = 0.003), whereas both the performance score (P < 0.001) and SUVmax (P = 0.022) were independently associated with OS. Conclusions Pretreatment primary tumor SUVmax on 18 F-FDG PET/CT predicts treatment outcomes in SGC patients. Definitive IMRT is an effective treatment strategy when organ function and cosmesis need to be preserved.
AB - Purpose The aim of this study was to investigate the prognostic significance of 18 F-FDG uptake in salivary gland carcinoma (SGC) patients treated with definitive intensity-modulated radiation therapy (IMRT). Methods We retrospectively examined 46 SGC patients who received pretreatment 18 F-FDG PET/CT and definitive IMRT between 2007 and 2014. Most tumors were located in the minor salivary glands (n = 35 [76%]). Forty-six percent (n = 21) of the participants had unresectable disease. The median radiation dose was 72 Gy. Treatment outcomes were examined in relation to clinicopathologic parameters and pretreatment primary tumor SUVmax on 18 F-FDG PET/CT. Results After a median follow-up of 54 months, the 5-year locoregional progression-free survival (LRPFS), distant metastasis-free survival, progression-free survival (PFS), and overall survival (OS) rates were 77%, 75%, 63%, and 61%, respectively. The median primary tumor SUVmax was 7.4 (range, 2.3-23.6), and the optimal cutoff value that maximized the prognostic significance for 5-year PFS was 7.4 (P = 0.006). Patients with a high SUVmax (≥7.4) had significantly lower 5-year LRPFS (P = 0.007), distant metastasis-free survival (P = 0.046), and OS (P = 0.013) rates than those with a low SUVmax (<7.4). Multivariate analyses identified SUVmax as the only independent predictor of LRPFS (P = 0.023) and PFS (P = 0.003), whereas both the performance score (P < 0.001) and SUVmax (P = 0.022) were independently associated with OS. Conclusions Pretreatment primary tumor SUVmax on 18 F-FDG PET/CT predicts treatment outcomes in SGC patients. Definitive IMRT is an effective treatment strategy when organ function and cosmesis need to be preserved.
KW - 18 F-FDG PET
KW - SUV
KW - definitive radiotherapy
KW - intensity-modulated radiation therapy
KW - salivary gland carcinoma
KW - treatment outcome
UR - http://www.scopus.com/inward/record.url?scp=85021271845&partnerID=8YFLogxK
U2 - 10.1097/RLU.0000000000001740
DO - 10.1097/RLU.0000000000001740
M3 - 文章
C2 - 28650891
AN - SCOPUS:85021271845
SN - 0363-9762
VL - 42
SP - 655
EP - 662
JO - Clinical Nuclear Medicine
JF - Clinical Nuclear Medicine
IS - 9
ER -