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Diagnostic accuracy of high resolution melting analysis for detection of KRAS mutations: a systematic review and meta-analysis
Increasing evidence points to a negative correlation between KRAS mutations and patients' responses to anti-EGFR monoclonal antibody treatment. Therefore, patients must undergo KRAS mutation detection to be eligible for treatment. High resolution melting analysis (HRM) is gaining increasing att...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4268648/ https://www.ncbi.nlm.nih.gov/pubmed/25515911 http://dx.doi.org/10.1038/srep07521 |
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author | Liu, Yue-Ping Wu, Hai-Yan Yang, Xiang Xu, Han-Qing Chen, Dong Huang, Qing Fu, Wei-Ling |
author_facet | Liu, Yue-Ping Wu, Hai-Yan Yang, Xiang Xu, Han-Qing Chen, Dong Huang, Qing Fu, Wei-Ling |
author_sort | Liu, Yue-Ping |
collection | PubMed |
description | Increasing evidence points to a negative correlation between KRAS mutations and patients' responses to anti-EGFR monoclonal antibody treatment. Therefore, patients must undergo KRAS mutation detection to be eligible for treatment. High resolution melting analysis (HRM) is gaining increasing attention in KRAS mutation detection. However, its accuracy has not been systematically evaluated. We conducted a meta-analysis of published articles, involving 13 articles with 1,520 samples, to assess its diagnostic accuracy compared with DNA sequencing. The quality of included articles was assessed using the revised Quality Assessment for Studies of Diagnostic Accuracy (QUADAS-2) tools. Random effects models were applied to analyze the performance of pooled characteristics. The overall sensitivity and specificity of HRM were 0.99 (95% confidence interval [CI]: 0.98–1.00) and 0.96 (95%CI: 0.94–0.97), respectively. The area under the summary receiver operating characteristic curve was 0.996. High sensitivity and specificity, less labor, rapid turn-around and the closed-tube format of HRM make it an attractive choice for rapid detection of KRAS mutations in clinical practice. The burden of DNA sequencing can be reduced dramatically by the implementation of HRM, but positive results still need to be sequenced for diagnostic confirmation. |
format | Online Article Text |
id | pubmed-4268648 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-42686482014-12-18 Diagnostic accuracy of high resolution melting analysis for detection of KRAS mutations: a systematic review and meta-analysis Liu, Yue-Ping Wu, Hai-Yan Yang, Xiang Xu, Han-Qing Chen, Dong Huang, Qing Fu, Wei-Ling Sci Rep Article Increasing evidence points to a negative correlation between KRAS mutations and patients' responses to anti-EGFR monoclonal antibody treatment. Therefore, patients must undergo KRAS mutation detection to be eligible for treatment. High resolution melting analysis (HRM) is gaining increasing attention in KRAS mutation detection. However, its accuracy has not been systematically evaluated. We conducted a meta-analysis of published articles, involving 13 articles with 1,520 samples, to assess its diagnostic accuracy compared with DNA sequencing. The quality of included articles was assessed using the revised Quality Assessment for Studies of Diagnostic Accuracy (QUADAS-2) tools. Random effects models were applied to analyze the performance of pooled characteristics. The overall sensitivity and specificity of HRM were 0.99 (95% confidence interval [CI]: 0.98–1.00) and 0.96 (95%CI: 0.94–0.97), respectively. The area under the summary receiver operating characteristic curve was 0.996. High sensitivity and specificity, less labor, rapid turn-around and the closed-tube format of HRM make it an attractive choice for rapid detection of KRAS mutations in clinical practice. The burden of DNA sequencing can be reduced dramatically by the implementation of HRM, but positive results still need to be sequenced for diagnostic confirmation. Nature Publishing Group 2014-12-17 /pmc/articles/PMC4268648/ /pubmed/25515911 http://dx.doi.org/10.1038/srep07521 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Article Liu, Yue-Ping Wu, Hai-Yan Yang, Xiang Xu, Han-Qing Chen, Dong Huang, Qing Fu, Wei-Ling Diagnostic accuracy of high resolution melting analysis for detection of KRAS mutations: a systematic review and meta-analysis |
title | Diagnostic accuracy of high resolution melting analysis for detection of KRAS mutations: a systematic review and meta-analysis |
title_full | Diagnostic accuracy of high resolution melting analysis for detection of KRAS mutations: a systematic review and meta-analysis |
title_fullStr | Diagnostic accuracy of high resolution melting analysis for detection of KRAS mutations: a systematic review and meta-analysis |
title_full_unstemmed | Diagnostic accuracy of high resolution melting analysis for detection of KRAS mutations: a systematic review and meta-analysis |
title_short | Diagnostic accuracy of high resolution melting analysis for detection of KRAS mutations: a systematic review and meta-analysis |
title_sort | diagnostic accuracy of high resolution melting analysis for detection of kras mutations: a systematic review and meta-analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4268648/ https://www.ncbi.nlm.nih.gov/pubmed/25515911 http://dx.doi.org/10.1038/srep07521 |
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