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Relationship Between 18F-Fluorodeoxyglucose Uptake and V-Ki-Ras2 Kirsten Rat Sarcoma Viral Oncogene Homolog Mutation in Colorectal Cancer Patients Variability Depending on C-Reactive Protein Level

Authors
 Jae-Hoon Lee  ;  Jeonghyun Kang  ;  Seung Hyuk Baik  ;  Kang Young Lee  ;  Beom Jin Lim  ;  Tae Joo Jeon  ;  Young Hoon Ryu  ;  Seung-Kook Sohn 
Citation
 Medicine, Vol.95(1) : 2236-2236, 2016 
Journal Title
 Medicine 
ISSN
 0025-7974 
Issue Date
2016
MeSH
Aged ; C-Reactive Protein/analysis* ; Colorectal Neoplasms/diagnostic imaging ; Colorectal Neoplasms/genetics* ; Colorectal Neoplasms/surgery ; Female ; Fluorodeoxyglucose F18/pharmacokinetics* ; Humans ; Male ; Middle Aged ; Multimodal Imaging ; Mutation ; Polymerase Chain Reaction ; Positron-Emission Tomography ; Proto-Oncogene Proteins p21(ras) ; Radiopharmaceuticals/pharmacokinetics* ; Sarcoma/diagnostic imaging ; Sarcoma/genetics* ; Sarcoma/surgery ; Tomography, X-Ray Computed
Abstract
To evaluate clinical values of clinicopathologic and 18F-fluorodeoxyglucose (18F-FDG) positron emission tomography/computed tomography (PET/CT)-related parameters for prediction of v-Ki-ras2 Kirsten rat sarcoma viral oncogene homolog (KRAS) mutation in colorectal cancer (CRC) and to investigate their variability depending on C-reactive protein (CRP) levels. In total, 179 CRC patients who underwent PET/CT scans before curative resection and KRAS mutation evaluation following surgery were enrolled. Maximum standardized uptake value (SUV max), peak standardized uptake value (SUV peak), metabolic tumor volume, and total lesion glycolysis were determined semiquantitatively. Associations between clinicopathologic and PET/CT-related parameters and KRAS expression were analyzed. Elevated CRP (> 6.0 mg/L; n = 47) was associated with higher primary tumor size, higher SUV max, SUV peak, metabolic tumor volume, and total lesion glycolysis, compared with those for the group with a CRP lower than that the cutoff value (< 6.0 mg/L; n = 132). Interestingly, the CRC patients (having CRP < 6.0 mg/L) with KRAS mutations had significantly higher (P < 0.05) SUV max and SUV peak values than the patients expressing wild-type KRAS mutations. Multivariate analysis revealed SUV max and SUV peak to be significantly associated with KRAS mutations (odds ratio = 3.3, P = 0.005, and odds ratio = 3.9, P = 0.004), together with histologic grade and lymph node metastasis. 18F-FDG uptake was significantly higher in CRC patients with KRAS mutations and with normal CRP levels. A severe local inflammation with raised CRP levels, however, might affect accurate 18F-FDG quantification in CRC tumors. Positron emission tomography/computed tomography-related parameters could supplement genomic analysis to determine KRAS expression in CRC; however, care should be exercised to guarantee proper patient selection.
Files in This Item:
T201600082.pdf Download
DOI
10.1097/MD.0000000000002236
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Surgery (외과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Nuclear Medicine (핵의학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
Yonsei Authors
강정현(Kang, Jeonghyun) ORCID logo https://orcid.org/0000-0001-7311-6053
백승혁(Baik, Seung Hyuk) ORCID logo https://orcid.org/0000-0003-4183-2332
손승국(Sohn, Seung Kook)
유영훈(Ryu, Young Hoon) ORCID logo https://orcid.org/0000-0002-9000-5563
이강영(Lee, Kang Young)
이재훈(Lee, Jae Hoon) ORCID logo https://orcid.org/0000-0002-9898-9886
임범진(Lim, Beom Jin) ORCID logo https://orcid.org/0000-0003-2856-0133
전태주(Jeon, Tae Joo) ORCID logo https://orcid.org/0000-0002-7574-6734
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URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/146250
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