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Can Serum be Used for Analyzing the KRAS Mutation Status in Patients with Advanced Colorectal Cancer?

Authors
Kim, Seung TaeChang, Won JinJin, LihuaSung, Jae SookChoi, Yun JiKim, Yeul Hong
Issue Date
Oct-2015
Publisher
KOREAN CANCER ASSOCIATION
Keywords
KRAS; Mutation; Serum; Neoplasms
Citation
CANCER RESEARCH AND TREATMENT, v.47, no.4, pp.796 - 803
Indexed
SCIE
SCOPUS
KCI
Journal Title
CANCER RESEARCH AND TREATMENT
Volume
47
Number
4
Start Page
796
End Page
803
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/92417
DOI
10.4143/crt.2014.106
ISSN
1598-2998
Abstract
Purpose KRAS mutations have been used widely as prognostic or predictive marker in patients with advanced colorectal cancer (CRC). However, it may be difficult to obtain a tumor tissue for analyzing the status of KRAS mutation in large proportion of patients with advanced disease. Materials and Methods We obtained pairs of tumor and serum samples from 65 patients with advanced CRC, between March 2008 and July 2011. KRAS mutation status from the tumor samples was analyzed by genomic polymerase chain reaction and direct sequence, and KRAS mutation status from the serum samples was determined by a genomic polymerase chain reaction restriction fragment length polymorphism assay. Results KRAS mutations were detected in the serum samples of 26 patients and in the tumor samples of 31 patients. KRAS mutation status in the serum and tumor samples was consistent in 44 of the 65 pairs (67.7%). There was a significant correlation between the mutations detected in the serum sample and the mutations detected in the matched tumor sample (correlation index, 0.35; p <0004) Twenty-two of the 57 patients (38.5%) received anti epidermal growth factor receptor therapy as any line therapy. There was no significant difference in the overall survival (OS) in accordance to the status of KRAS mutations in both the serum and tumor samples (p > 0.05). In a multivariate analysis, liver metastasis and no cytoreductive operation were independent prognostic factors for decreased OS. Conclusion The serum sample might alternatively be used when it is difficult to obtain tumoi issues for analyzing the status of KRAS mutation in patients with advanced CRC.
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