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Published in: Abdominal Radiology 6/2017

01-06-2017

Correlation between KRAS mutation and 18F-FDG uptake in stage IV colorectal cancer

Authors: Arthur Cho, Kwanhyeong Jo, Sang Hyun Hwang, Narae Lee, Minkyu Jung, Mijin Yun, Hee Sung Hwang

Published in: Abdominal Radiology | Issue 6/2017

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Abstract

Purpose

The purpose of this study is to evaluate the correlation between KRAS mutation, 18F-FDG uptake, and metastatic pattern in advanced stage colorectal cancer (CRC) patients.

Methods

Medical records of stage IV CRC patients who underwent 18F-FDG PET/CT for staging and KRAS mutation analysis were selected. On PET scans, a volume of interest (VOI) was drawn on the primary lesion. 18F-FDG indices (SUVmax, SUVmean, MTV, TLG) of the primary lesions were obtained and correlated with KRAS mutation of the primary lesion. Also, metastatic sites were recorded. Association between metastatic pattern and KRAS expression and FDG indices were analyzed.

Results

KRAS mutation was positive in 40 (43%) patients. Evaluation of FDG indices showed that higher SUVmax (14.0 vs. 11.2, p = 0.004), higher SUVmean (5.3 vs. 4.7, p = 0.005), and higher TLG (301.4 vs. 205.5, p = 0.023) were predictive of KRAS mutation compared to wild-type (WT) KRAS. Lung metastasis was more frequently involved in patients with KRAS mutation (50.0% vs. 22.6%, p = 0.006), and liver metastasis was more frequently involved in patients with WT KRAS (81.1% vs. 55.0%, p = 0.007). Multivariate analysis showed that  primary tumor location (OR 3.92, p = 0.07) and KRAS mutation (OR 2.45, p = 0.09) were significant factors in lung metastasis model.

Conclusion

KRAS mutation patients had more frequent lung metastasis and had higher 18F-FDG uptake compared to WT KRAS in stage IV CRC.
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Metadata
Title
Correlation between KRAS mutation and 18F-FDG uptake in stage IV colorectal cancer
Authors
Arthur Cho
Kwanhyeong Jo
Sang Hyun Hwang
Narae Lee
Minkyu Jung
Mijin Yun
Hee Sung Hwang
Publication date
01-06-2017
Publisher
Springer US
Published in
Abdominal Radiology / Issue 6/2017
Print ISSN: 2366-004X
Electronic ISSN: 2366-0058
DOI
https://doi.org/10.1007/s00261-017-1054-2

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