Comparison between FDG Uptake and Pathologic or Immunohistochemical Parametersin Pre-operative PET/CT Scan of Patient with Primary Colorectal Cancer.
- Author:
Sae Jung NA
1
;
Yong An CHUNG
;
Lee So MAENG
;
Ki Jun KIM
;
Kyung Myung SOHN
;
Sung Hoon KIM
;
Hyung Sun SOHN
;
Soo Kyo CHUNG
Author Information
1. Department of Radiology, College of Medicine, The Catholic University of Korea, Seoul, Korea. sminee@cnuh.co.kr
- Publication Type:Original Article
- Keywords:
Colorectal cancer;
F-18 FDG;
PET/CT
- MeSH:
Colorectal Neoplasms;
Humans;
Lymph Nodes;
Neoplasm Metastasis
- From:Nuclear Medicine and Molecular Imaging
2009;43(6):557-564
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
PURPOSE: To evaluate the relationship between F-18 FDG uptake of tumor in PET/CT scan and pathological or immunohistochemial parameters of colorectal cancer. MATERIALS AND METHODS: 147 colorectal cancer patients who underwent both pre-operative F-18 FDG PET/CT scan and surgery were included. In cases with perceptible FDG uptake in primary tumor, the maximum standardized uptake value (SUVmax) was calculated. The pathologic results such as site, size, depth of invasion (T stage), growth pattern, differentiation of primary tumor, lymph node metastasis and Dukes-Astler & Coller stage and immunohistochemical markers such as expression of EGFR, MLH1, MSH2 and Ki-67 index were reviewed. RESULTS: 146 out of 147 PET/CT scans with colorectal cancer showed perceptible focal FDG uptake. SUVmax showed mild positive linear correlation with size of primary tumor (r=0.277, p=0.001) and Ki-67 index (r=0.226, p=0.019). No significant difference in F-18 FDG uptake was found according to site, depth of invasion (T stage), growth pattern, differentiation of primary tumor, presence of lymph node metastasis, Dukes-Astler & Coller stage and expression of EGFR. CONCLUSION: The degree of F-18 FDG uptake in colorectal cancer was associated with the size and the degree of Ki-67 index of primary tumor. It could be thought that FDG uptake of primary tumor has a correlation with macroscopic and microscopic tumor growth.
