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Epidermal growth factor receptor (EGFR) mutations are exceptionally rare in thyroid transcription factor (TTF-1)-negative adenocarcinomas of the lung

INTRODUCTION: Approximately 70% of lung adenocarcinomas express TTF-1. EGFR mutations are present in 13-15% of Western adenocarcinoma patients. This paper investigates TTF1 as a negative predictor of mutant EGFR in lung adenocarcinomas. RESULTS: In the pilot cohort (N = 301) two of 224 specimens pos...

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Autores principales: Somaiah, Neeta, Fidler, Mary Jo, Garrett-Mayer, Elizabeth, Wahlquist, Amy, Shirai, Keisuke, Buckingham, Lela, Hensing, Thomas, Bonomi, Philip, Simon, George R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4278331/
https://www.ncbi.nlm.nih.gov/pubmed/25594059
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author Somaiah, Neeta
Fidler, Mary Jo
Garrett-Mayer, Elizabeth
Wahlquist, Amy
Shirai, Keisuke
Buckingham, Lela
Hensing, Thomas
Bonomi, Philip
Simon, George R.
author_facet Somaiah, Neeta
Fidler, Mary Jo
Garrett-Mayer, Elizabeth
Wahlquist, Amy
Shirai, Keisuke
Buckingham, Lela
Hensing, Thomas
Bonomi, Philip
Simon, George R.
author_sort Somaiah, Neeta
collection PubMed
description INTRODUCTION: Approximately 70% of lung adenocarcinomas express TTF-1. EGFR mutations are present in 13-15% of Western adenocarcinoma patients. This paper investigates TTF1 as a negative predictor of mutant EGFR in lung adenocarcinomas. RESULTS: In the pilot cohort (N = 301) two of 224 specimens positive for EGFR mutations had negative TTF-1 expression (sensitivity 99.1%, 95% confidence interval (CI) 96.8-99.9%). Estimated negative predictive values (NPV) for EGFR mutation prevalence rates of 13% and 15% are 99.5% (95% credible interval (CRI) 98.6%-99.9%) and 99.4% (CRI – 98.4%-99.9%). For EGFR mutation rates of 13% and 15%, using validation cohort data (211 patients), the estimated NPVs were 97% (95% CRI 92%-99%) and 96% (95% CRI 91%-99%). METHODS: Formalin-fixed paraffin-embedded tumors from lung adenocarcinoma patients were analyzed for EGFR mutations by allele-specific PCR in the ‘pilot cohort’. TTF-1 status was documented as positive or negative. Negative predictive value (NPV) for a range of true prevalence of EGFR mutation (1%-50%) was estimated using Bayesian modeling. The hypothesis was validated in a separate ‘validation’ cohort using the same modeling. CONCLUSION: An overwhelming majority of TTF-1 negative adenocarcinomas will be negative for EGFR mutations. This finding allows for earlier initiation of chemotherapy in newly diagnosed TTF-1 negative adenocarcinomas of the lung with stage IV disease.
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spelling pubmed-42783312015-01-15 Epidermal growth factor receptor (EGFR) mutations are exceptionally rare in thyroid transcription factor (TTF-1)-negative adenocarcinomas of the lung Somaiah, Neeta Fidler, Mary Jo Garrett-Mayer, Elizabeth Wahlquist, Amy Shirai, Keisuke Buckingham, Lela Hensing, Thomas Bonomi, Philip Simon, George R. Oncoscience Clinical Report INTRODUCTION: Approximately 70% of lung adenocarcinomas express TTF-1. EGFR mutations are present in 13-15% of Western adenocarcinoma patients. This paper investigates TTF1 as a negative predictor of mutant EGFR in lung adenocarcinomas. RESULTS: In the pilot cohort (N = 301) two of 224 specimens positive for EGFR mutations had negative TTF-1 expression (sensitivity 99.1%, 95% confidence interval (CI) 96.8-99.9%). Estimated negative predictive values (NPV) for EGFR mutation prevalence rates of 13% and 15% are 99.5% (95% credible interval (CRI) 98.6%-99.9%) and 99.4% (CRI – 98.4%-99.9%). For EGFR mutation rates of 13% and 15%, using validation cohort data (211 patients), the estimated NPVs were 97% (95% CRI 92%-99%) and 96% (95% CRI 91%-99%). METHODS: Formalin-fixed paraffin-embedded tumors from lung adenocarcinoma patients were analyzed for EGFR mutations by allele-specific PCR in the ‘pilot cohort’. TTF-1 status was documented as positive or negative. Negative predictive value (NPV) for a range of true prevalence of EGFR mutation (1%-50%) was estimated using Bayesian modeling. The hypothesis was validated in a separate ‘validation’ cohort using the same modeling. CONCLUSION: An overwhelming majority of TTF-1 negative adenocarcinomas will be negative for EGFR mutations. This finding allows for earlier initiation of chemotherapy in newly diagnosed TTF-1 negative adenocarcinomas of the lung with stage IV disease. Impact Journals LLC 2014-08-07 /pmc/articles/PMC4278331/ /pubmed/25594059 Text en © 2014 Somaiah et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Clinical Report
Somaiah, Neeta
Fidler, Mary Jo
Garrett-Mayer, Elizabeth
Wahlquist, Amy
Shirai, Keisuke
Buckingham, Lela
Hensing, Thomas
Bonomi, Philip
Simon, George R.
Epidermal growth factor receptor (EGFR) mutations are exceptionally rare in thyroid transcription factor (TTF-1)-negative adenocarcinomas of the lung
title Epidermal growth factor receptor (EGFR) mutations are exceptionally rare in thyroid transcription factor (TTF-1)-negative adenocarcinomas of the lung
title_full Epidermal growth factor receptor (EGFR) mutations are exceptionally rare in thyroid transcription factor (TTF-1)-negative adenocarcinomas of the lung
title_fullStr Epidermal growth factor receptor (EGFR) mutations are exceptionally rare in thyroid transcription factor (TTF-1)-negative adenocarcinomas of the lung
title_full_unstemmed Epidermal growth factor receptor (EGFR) mutations are exceptionally rare in thyroid transcription factor (TTF-1)-negative adenocarcinomas of the lung
title_short Epidermal growth factor receptor (EGFR) mutations are exceptionally rare in thyroid transcription factor (TTF-1)-negative adenocarcinomas of the lung
title_sort epidermal growth factor receptor (egfr) mutations are exceptionally rare in thyroid transcription factor (ttf-1)-negative adenocarcinomas of the lung
topic Clinical Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4278331/
https://www.ncbi.nlm.nih.gov/pubmed/25594059
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