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Fully automated real-time PCR for EGFR testing in non-small cell lung carcinoma
Molecular testing for mutations in the EGFR gene is commonplace for patients with non-small cell lung cancer (NSCLC). These patients are often very sick and management decisions need to be made urgently. In many cases, the results of molecular testing are needed the same day, in order to start targe...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6349793/ https://www.ncbi.nlm.nih.gov/pubmed/30470932 http://dx.doi.org/10.1007/s00428-018-2486-y |
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author | Colling, Richard Bancroft, Hollie Langman, Gerald Soilleux, Elizabeth |
author_facet | Colling, Richard Bancroft, Hollie Langman, Gerald Soilleux, Elizabeth |
author_sort | Colling, Richard |
collection | PubMed |
description | Molecular testing for mutations in the EGFR gene is commonplace for patients with non-small cell lung cancer (NSCLC). These patients are often very sick and management decisions need to be made urgently. In many cases, the results of molecular testing are needed the same day, in order to start targeted therapy and allow maximum benefit for patients. The Idylla™ EGFR Mutation Test offers rapid results within three hours of requesting. This study aimed to assess the concordance of Idylla™ EGFR Mutation Test results with current standard tests. Forty formalin-fixed, paraffin-embedded NSCLC tumour cases (20 EGFR mutant and EGFR 20 wild type) were analysed by the Idylla™ EGFR Mutation Test (CE-IVD) and compared with PCR and NGS methodologies. The overall concordance between Idylla™ and standard testing was 92.5% (95% CI 80.14% to 97.42%) and the specificity of Idylla™ was 100% (95% CI 83.89% to 100%). The sensitivity was affected by loss of tumour content in tissue blocks in a small number of NGS cases; however, comparing Idylla™ with PCR alone, there was 100% concordance (95% CI 89.85% to 100%). The Idylla™ EGFR Mutation Test shows comparative accuracy to routine PCR testing for the most common EGFR mutations in NSCLC. The Idylla™ also offers significantly reduced turn-around times compared with existing modalities and therefore the platform would be a useful addition to many molecular diagnostics units. |
format | Online Article Text |
id | pubmed-6349793 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-63497932019-02-15 Fully automated real-time PCR for EGFR testing in non-small cell lung carcinoma Colling, Richard Bancroft, Hollie Langman, Gerald Soilleux, Elizabeth Virchows Arch Original Article Molecular testing for mutations in the EGFR gene is commonplace for patients with non-small cell lung cancer (NSCLC). These patients are often very sick and management decisions need to be made urgently. In many cases, the results of molecular testing are needed the same day, in order to start targeted therapy and allow maximum benefit for patients. The Idylla™ EGFR Mutation Test offers rapid results within three hours of requesting. This study aimed to assess the concordance of Idylla™ EGFR Mutation Test results with current standard tests. Forty formalin-fixed, paraffin-embedded NSCLC tumour cases (20 EGFR mutant and EGFR 20 wild type) were analysed by the Idylla™ EGFR Mutation Test (CE-IVD) and compared with PCR and NGS methodologies. The overall concordance between Idylla™ and standard testing was 92.5% (95% CI 80.14% to 97.42%) and the specificity of Idylla™ was 100% (95% CI 83.89% to 100%). The sensitivity was affected by loss of tumour content in tissue blocks in a small number of NGS cases; however, comparing Idylla™ with PCR alone, there was 100% concordance (95% CI 89.85% to 100%). The Idylla™ EGFR Mutation Test shows comparative accuracy to routine PCR testing for the most common EGFR mutations in NSCLC. The Idylla™ also offers significantly reduced turn-around times compared with existing modalities and therefore the platform would be a useful addition to many molecular diagnostics units. Springer Berlin Heidelberg 2018-11-23 2019 /pmc/articles/PMC6349793/ /pubmed/30470932 http://dx.doi.org/10.1007/s00428-018-2486-y Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Colling, Richard Bancroft, Hollie Langman, Gerald Soilleux, Elizabeth Fully automated real-time PCR for EGFR testing in non-small cell lung carcinoma |
title | Fully automated real-time PCR for EGFR testing in non-small cell lung carcinoma |
title_full | Fully automated real-time PCR for EGFR testing in non-small cell lung carcinoma |
title_fullStr | Fully automated real-time PCR for EGFR testing in non-small cell lung carcinoma |
title_full_unstemmed | Fully automated real-time PCR for EGFR testing in non-small cell lung carcinoma |
title_short | Fully automated real-time PCR for EGFR testing in non-small cell lung carcinoma |
title_sort | fully automated real-time pcr for egfr testing in non-small cell lung carcinoma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6349793/ https://www.ncbi.nlm.nih.gov/pubmed/30470932 http://dx.doi.org/10.1007/s00428-018-2486-y |
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