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Can Serum be Used for Analyzing the KRAS Mutation Status in Patients with Advanced Colorectal Cancer?
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 MET...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Cancer Association
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4614179/ https://www.ncbi.nlm.nih.gov/pubmed/25687873 http://dx.doi.org/10.4143/crt.2014.106 |
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author | Kim, Seung Tae Chang, Won Jin Jin, Lihua Sung, Jae Sook Choi, Yun Ji Kim, Yeul Hong |
author_facet | Kim, Seung Tae Chang, Won Jin Jin, Lihua Sung, Jae Sook Choi, Yun Ji Kim, Yeul Hong |
author_sort | Kim, Seung Tae |
collection | PubMed |
description | 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 KRASmutation 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 < 0.004). 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 KRASmutations 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 tumor tissues for analyzing the status of KRAS mutation in patients with advanced CRC. |
format | Online Article Text |
id | pubmed-4614179 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Korean Cancer Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-46141792015-10-22 Can Serum be Used for Analyzing the KRAS Mutation Status in Patients with Advanced Colorectal Cancer? Kim, Seung Tae Chang, Won Jin Jin, Lihua Sung, Jae Sook Choi, Yun Ji Kim, Yeul Hong Cancer Res Treat Original Article 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 KRASmutation 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 < 0.004). 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 KRASmutations 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 tumor tissues for analyzing the status of KRAS mutation in patients with advanced CRC. Korean Cancer Association 2015-10 2015-01-30 /pmc/articles/PMC4614179/ /pubmed/25687873 http://dx.doi.org/10.4143/crt.2014.106 Text en Copyright © 2015 by the Korean Cancer Association This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kim, Seung Tae Chang, Won Jin Jin, Lihua Sung, Jae Sook Choi, Yun Ji Kim, Yeul Hong Can Serum be Used for Analyzing the KRAS Mutation Status in Patients with Advanced Colorectal Cancer? |
title | Can Serum be Used for Analyzing the KRAS Mutation Status in Patients with Advanced Colorectal Cancer? |
title_full | Can Serum be Used for Analyzing the KRAS Mutation Status in Patients with Advanced Colorectal Cancer? |
title_fullStr | Can Serum be Used for Analyzing the KRAS Mutation Status in Patients with Advanced Colorectal Cancer? |
title_full_unstemmed | Can Serum be Used for Analyzing the KRAS Mutation Status in Patients with Advanced Colorectal Cancer? |
title_short | Can Serum be Used for Analyzing the KRAS Mutation Status in Patients with Advanced Colorectal Cancer? |
title_sort | can serum be used for analyzing the kras mutation status in patients with advanced colorectal cancer? |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4614179/ https://www.ncbi.nlm.nih.gov/pubmed/25687873 http://dx.doi.org/10.4143/crt.2014.106 |
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