TY - JOUR
T1 - F-18 FDG PET/CT contributes to more accurate detection of lymph nodal metastasis from actively proliferating esophageal squamous cell carcinoma
AU - Tanabe, Shunsuke
AU - Naomoto, Yoshio
AU - Shirakawa, Yasuhiro
AU - Fujiwara, Yasuhiro
AU - Sakurama, Kazufumi
AU - Noma, Kazuhiro
AU - Takaoka, Munenori
AU - Yamatsuji, Tomoki
AU - Hiraki, Takao
AU - Okumura, Yoshihiro
AU - Mitani, Masahiko
AU - Kaji, Mitsumasa
AU - Kanazawa, Susumu
AU - Fujiwara, Toshiyoshi
PY - 2011/10
Y1 - 2011/10
N2 - Purpose: Evaluating the status of disease progression is critical for planning a therapeutic strategy for esophageal cancer. In this regard, F-18 fluorodeoxyglucose-labeled positron emission tomography (PET) is one of the most useful diagnostic modalities. However, there is room to improve its diagnostic performance, such as distinguishing lymph nodal metastases from false positives. In this study, we examined the diagnostic accuracy of fluorodeoxyglucose PET accompanied by computed tomography imaging (PET/CT) to detect regional lymph nodal metastasis from esophageal squamous cell carcinoma (ESCC). Methods: A total of 102 patients diagnosed as ESCC were subjected to this study. These patients had a preoperative PET/CT examination to evaluate the existence of metastasis. The values of maximum standardized uptake value (SUV max) in primary tumors and in metastasized lymph nodes were measured to analyze their relationship with various clinicopathologic characteristics including the status of tumor cell proliferation, which was assessed by immunohistochemistry for Ki-67. Results: The SUV max of the primary tumor was positively correlated with tumor size and vessel invasion, and was positively related with the SUV max of lymph nodal metastasis, especially in cases of poorly differentiated ESCC. The SUV max of metastasized lymph nodes was higher in larger-sized metastasized lymph nodes, whereas the Ki-labeling index of lymph nodal metastasis was positively related with the SUV max per unit area (SUV max/mm 2). The diagnostic accuracy of PET/CT (87.3%) was higher than that of conventional CT scans (78.4%). Conclusions: The improved diagnostic accuracy of PET/CT can be explained by its ability to detect actively progressive metastasis at an early phase regardless of size.
AB - Purpose: Evaluating the status of disease progression is critical for planning a therapeutic strategy for esophageal cancer. In this regard, F-18 fluorodeoxyglucose-labeled positron emission tomography (PET) is one of the most useful diagnostic modalities. However, there is room to improve its diagnostic performance, such as distinguishing lymph nodal metastases from false positives. In this study, we examined the diagnostic accuracy of fluorodeoxyglucose PET accompanied by computed tomography imaging (PET/CT) to detect regional lymph nodal metastasis from esophageal squamous cell carcinoma (ESCC). Methods: A total of 102 patients diagnosed as ESCC were subjected to this study. These patients had a preoperative PET/CT examination to evaluate the existence of metastasis. The values of maximum standardized uptake value (SUV max) in primary tumors and in metastasized lymph nodes were measured to analyze their relationship with various clinicopathologic characteristics including the status of tumor cell proliferation, which was assessed by immunohistochemistry for Ki-67. Results: The SUV max of the primary tumor was positively correlated with tumor size and vessel invasion, and was positively related with the SUV max of lymph nodal metastasis, especially in cases of poorly differentiated ESCC. The SUV max of metastasized lymph nodes was higher in larger-sized metastasized lymph nodes, whereas the Ki-labeling index of lymph nodal metastasis was positively related with the SUV max per unit area (SUV max/mm 2). The diagnostic accuracy of PET/CT (87.3%) was higher than that of conventional CT scans (78.4%). Conclusions: The improved diagnostic accuracy of PET/CT can be explained by its ability to detect actively progressive metastasis at an early phase regardless of size.
KW - Esophageal cancer
KW - F-18 fluorodeoxy glucose (FDG)
KW - Lymph nodal metastasis
KW - Positron emission tomography (PET)
KW - Proliferation
KW - Squamous cell carcinoma
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U2 - 10.1097/RLU.0b013e318217adc9
DO - 10.1097/RLU.0b013e318217adc9
M3 - Article
C2 - 21892033
AN - SCOPUS:80053598556
SN - 0363-9762
VL - 36
SP - 854
EP - 859
JO - Clinical Nuclear Medicine
JF - Clinical Nuclear Medicine
IS - 10
ER -