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Lung cancer mutation testing: a clinical retesting study of agreement between a real-time PCR and a mass spectrometry test

To investigate the clinical validity and utility of tests for detecting Epidermal Growth Factor Receptor (EGFR) gene mutations in non-squamous non-small cell lung cancer patients, tumour DNA extracts from 532 patients previously tested by the cobas EGFR Mutation Test (RT-PCR test) were retested by t...

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Autores principales: Shepherd, Phillip, Sheath, Karen L., Tin, Sandar Tin, Khwaounjoo, Prashannata, Aye, Phyu S., Li, Angie, Laking, George R., Kingston, Nicola J., Lewis, Christopher A., Mark Elwood, J., Love, Donald R., McKeage, Mark J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5731886/
https://www.ncbi.nlm.nih.gov/pubmed/29254176
http://dx.doi.org/10.18632/oncotarget.21023
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author Shepherd, Phillip
Sheath, Karen L.
Tin, Sandar Tin
Khwaounjoo, Prashannata
Aye, Phyu S.
Li, Angie
Laking, George R.
Kingston, Nicola J.
Lewis, Christopher A.
Mark Elwood, J.
Love, Donald R.
McKeage, Mark J.
author_facet Shepherd, Phillip
Sheath, Karen L.
Tin, Sandar Tin
Khwaounjoo, Prashannata
Aye, Phyu S.
Li, Angie
Laking, George R.
Kingston, Nicola J.
Lewis, Christopher A.
Mark Elwood, J.
Love, Donald R.
McKeage, Mark J.
author_sort Shepherd, Phillip
collection PubMed
description To investigate the clinical validity and utility of tests for detecting Epidermal Growth Factor Receptor (EGFR) gene mutations in non-squamous non-small cell lung cancer patients, tumour DNA extracts from 532 patients previously tested by the cobas EGFR Mutation Test (RT-PCR test) were retested by the Sequenom/Agena Biosciences MassArray OncoFocus mass spectrometry test (MS test). Valid results from both tests were available from 470 patients (88%) for agreement analysis. Survival data were obtained for 513 patients (96%) and 77 patients (14%) were treated with EGFR tyrosine kinase inhibitors (TKIs). Agreement analysis revealed moderately high positive (79.8%), negative (96.9%) and overall percentage agreement (93.2%) for the detection of EGFR mutations. However, EGFR mutations were detected by one test and not by the other test in 32 patients (7%). Retesting of discordant samples revealed false-positive and false-negative results generated by both tests. Despite this, treatment and survival outcomes correlated with the results of the RT-PCR and MS tests. In conclusion, this study provides evidence of the clinical validity and utility of the RT-PCR and MS tests for detection of EGFR mutations that predict prognosis and benefit from EGFR-TKI treatment. However, their false-positive and false-negative test results may have important clinical consequences.
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spelling pubmed-57318862017-12-17 Lung cancer mutation testing: a clinical retesting study of agreement between a real-time PCR and a mass spectrometry test Shepherd, Phillip Sheath, Karen L. Tin, Sandar Tin Khwaounjoo, Prashannata Aye, Phyu S. Li, Angie Laking, George R. Kingston, Nicola J. Lewis, Christopher A. Mark Elwood, J. Love, Donald R. McKeage, Mark J. Oncotarget Research Paper To investigate the clinical validity and utility of tests for detecting Epidermal Growth Factor Receptor (EGFR) gene mutations in non-squamous non-small cell lung cancer patients, tumour DNA extracts from 532 patients previously tested by the cobas EGFR Mutation Test (RT-PCR test) were retested by the Sequenom/Agena Biosciences MassArray OncoFocus mass spectrometry test (MS test). Valid results from both tests were available from 470 patients (88%) for agreement analysis. Survival data were obtained for 513 patients (96%) and 77 patients (14%) were treated with EGFR tyrosine kinase inhibitors (TKIs). Agreement analysis revealed moderately high positive (79.8%), negative (96.9%) and overall percentage agreement (93.2%) for the detection of EGFR mutations. However, EGFR mutations were detected by one test and not by the other test in 32 patients (7%). Retesting of discordant samples revealed false-positive and false-negative results generated by both tests. Despite this, treatment and survival outcomes correlated with the results of the RT-PCR and MS tests. In conclusion, this study provides evidence of the clinical validity and utility of the RT-PCR and MS tests for detection of EGFR mutations that predict prognosis and benefit from EGFR-TKI treatment. However, their false-positive and false-negative test results may have important clinical consequences. Impact Journals LLC 2017-09-16 /pmc/articles/PMC5731886/ /pubmed/29254176 http://dx.doi.org/10.18632/oncotarget.21023 Text en Copyright: © 2017 Shepherd et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Shepherd, Phillip
Sheath, Karen L.
Tin, Sandar Tin
Khwaounjoo, Prashannata
Aye, Phyu S.
Li, Angie
Laking, George R.
Kingston, Nicola J.
Lewis, Christopher A.
Mark Elwood, J.
Love, Donald R.
McKeage, Mark J.
Lung cancer mutation testing: a clinical retesting study of agreement between a real-time PCR and a mass spectrometry test
title Lung cancer mutation testing: a clinical retesting study of agreement between a real-time PCR and a mass spectrometry test
title_full Lung cancer mutation testing: a clinical retesting study of agreement between a real-time PCR and a mass spectrometry test
title_fullStr Lung cancer mutation testing: a clinical retesting study of agreement between a real-time PCR and a mass spectrometry test
title_full_unstemmed Lung cancer mutation testing: a clinical retesting study of agreement between a real-time PCR and a mass spectrometry test
title_short Lung cancer mutation testing: a clinical retesting study of agreement between a real-time PCR and a mass spectrometry test
title_sort lung cancer mutation testing: a clinical retesting study of agreement between a real-time pcr and a mass spectrometry test
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5731886/
https://www.ncbi.nlm.nih.gov/pubmed/29254176
http://dx.doi.org/10.18632/oncotarget.21023
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