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EGFR fluorescence in situ hybridisation assay: guidelines for application to non-small-cell lung cancer
There is a need for predictive biomarkers that identify non-small-cell lung cancer (NSCLC) patients most likely to respond to epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) treatment. There are numerous potential candidates, although none has been proven in prospective clini...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BMJ Group
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2771853/ https://www.ncbi.nlm.nih.gov/pubmed/19861557 http://dx.doi.org/10.1136/jcp.2009.066548 |
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author | Varella-Garcia, M Diebold, J Eberhard, D A Geenen, K Hirschmann, A Kockx, M Nagelmeier, I Rüschoff, J Schmitt, M Arbogast, S Cappuzzo, F |
author_facet | Varella-Garcia, M Diebold, J Eberhard, D A Geenen, K Hirschmann, A Kockx, M Nagelmeier, I Rüschoff, J Schmitt, M Arbogast, S Cappuzzo, F |
author_sort | Varella-Garcia, M |
collection | PubMed |
description | There is a need for predictive biomarkers that identify non-small-cell lung cancer (NSCLC) patients most likely to respond to epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) treatment. There are numerous potential candidates, although none has been proven in prospective clinical trials. The EGFR gene copy number evaluated by fluorescence in situ hybridisation (FISH) has been highlighted as one of the most effective markers for sensitivity to EGFR TKIs in large phase III, randomised placebo-controlled trials and has been used in clinical settings to assist physicians in defining the therapeutic regimen. The EGFR FISH assay has technical challenges and it is critical that detailed guidelines are provided to help clinical laboratories in performing and interpreting the test. Excellent assay reproducibility and portability rates among laboratories are crucial to guarantee that accurate clinical decisions can be made for patients with NSCLC. This article discusses the consensus outcomes of a global workshop convened to discuss key technical issues and standardise reading strategies for the EGFR FISH assay of NSCLC tumour tissue. |
format | Text |
id | pubmed-2771853 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BMJ Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-27718532009-11-16 EGFR fluorescence in situ hybridisation assay: guidelines for application to non-small-cell lung cancer Varella-Garcia, M Diebold, J Eberhard, D A Geenen, K Hirschmann, A Kockx, M Nagelmeier, I Rüschoff, J Schmitt, M Arbogast, S Cappuzzo, F J Clin Pathol Reviews There is a need for predictive biomarkers that identify non-small-cell lung cancer (NSCLC) patients most likely to respond to epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) treatment. There are numerous potential candidates, although none has been proven in prospective clinical trials. The EGFR gene copy number evaluated by fluorescence in situ hybridisation (FISH) has been highlighted as one of the most effective markers for sensitivity to EGFR TKIs in large phase III, randomised placebo-controlled trials and has been used in clinical settings to assist physicians in defining the therapeutic regimen. The EGFR FISH assay has technical challenges and it is critical that detailed guidelines are provided to help clinical laboratories in performing and interpreting the test. Excellent assay reproducibility and portability rates among laboratories are crucial to guarantee that accurate clinical decisions can be made for patients with NSCLC. This article discusses the consensus outcomes of a global workshop convened to discuss key technical issues and standardise reading strategies for the EGFR FISH assay of NSCLC tumour tissue. BMJ Group 2009-11 2009-10-20 /pmc/articles/PMC2771853/ /pubmed/19861557 http://dx.doi.org/10.1136/jcp.2009.066548 Text en © Varella-Garcia et al 2009 http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Reviews Varella-Garcia, M Diebold, J Eberhard, D A Geenen, K Hirschmann, A Kockx, M Nagelmeier, I Rüschoff, J Schmitt, M Arbogast, S Cappuzzo, F EGFR fluorescence in situ hybridisation assay: guidelines for application to non-small-cell lung cancer |
title | EGFR fluorescence in situ hybridisation assay: guidelines for application to non-small-cell lung cancer |
title_full | EGFR fluorescence in situ hybridisation assay: guidelines for application to non-small-cell lung cancer |
title_fullStr | EGFR fluorescence in situ hybridisation assay: guidelines for application to non-small-cell lung cancer |
title_full_unstemmed | EGFR fluorescence in situ hybridisation assay: guidelines for application to non-small-cell lung cancer |
title_short | EGFR fluorescence in situ hybridisation assay: guidelines for application to non-small-cell lung cancer |
title_sort | egfr fluorescence in situ hybridisation assay: guidelines for application to non-small-cell lung cancer |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2771853/ https://www.ncbi.nlm.nih.gov/pubmed/19861557 http://dx.doi.org/10.1136/jcp.2009.066548 |
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