1.Recent Chemotherapy Reduces the Maximum-Standardized Uptake Value of 18F-Fluoro-Deoxyglucose Positron Emission Tomography in Colorectal Cancer.
Minjong LEE ; Tae Sung YEUM ; Ji Won KIM ; Sohee OH ; Shin Ae LEE ; Hong Ran MOON ; Young Hoon CHOI ; Yoo Min HAN ; Ji Min CHOI ; Dong Kee JANG
Gut and Liver 2014;8(3):254-264
BACKGROUND/AIMS: The aim of this study was to evaluate the influence of recent chemotherapy on the patterns of the maximum-standardized uptake value (M-SUV) and sensitivity of 18F-fluoro-deoxyglucose positron emission tomography/computed tomography (18F-FDG-PET/CT) in colorectal cancer. METHODS: We retrospectively analyzed the FDG-PET/CT of 509 patients who underwent surgery for colorectal cancer. Subgroup analysis was performed according to chemotherapy status; 401 patients were not treated with chemotherapy and 108 patients were treated with chemotherapy within 6 months prior to surgery. Pathologic analysis of the surgical specimen was used as the gold standard. RESULTS: The M-SUV was significantly lower in patients treated with chemotherapy than in those not treated with chemotherapy in pathologically confirmed same stages of disease. The difference in the sensitivity of the M-SUV according to chemotherapy status was greatest using a cutoff M-SUV value of 6.4 (p<0.001). The longest diameter of the primary tumor was the most important factor that correlated with M-SUV of the primary tumor irrespective of the chemotherapy effect (p<0.001). The M-SUV of the primary tumor was not an independent predictor of lymph node metastasis in colorectal cancer. CONCLUSIONS: The results indicate that the M-SUV of FDG-PET/CT should be interpreted in the context of concurrent chemotherapy.
Aged
;
Antineoplastic Agents/*adverse effects
;
Chemoradiotherapy, Adjuvant/adverse effects
;
Chemotherapy, Adjuvant/adverse effects
;
Colorectal Neoplasms/drug therapy/pathology/*radionuclide imaging
;
Female
;
Fluorodeoxyglucose F18/diagnostic use/*pharmacology
;
Humans
;
Male
;
Neoplasm Invasiveness
;
Neoplasm Metastasis
;
Positron-Emission Tomography/methods
;
Radiopharmaceuticals/diagnostic use/*pharmacology
;
Retrospective Studies