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Prevalence of K-RAS Codons 12 and 13 Mutations in Locally Advanced Head and Neck Squamous Cell Carcinoma and Impact on Clinical Outcomes

Background. RAS gene mutations have an impact on treatment response and overall prognosis for certain types of cancer. Objectives. To determine the prevalence and impact of K-RAS codons 12 and 13 mutations in patients with locally advanced HNSCC treated with primary or adjuvant chemo-radiation. Meth...

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Autores principales: Bissada, Eric, Abboud, Olivier, Abou Chacra, Zahi, Guertin, Louis, Weng, Xiaoduan, Nguyen-Tan, Phuc Félix, Tabet, Jean-Claude, Thibaudeau, Ève, Lambert, Louise, Audet, Marie-Lise, Fortin, Bernard, Soulières, Denis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3657450/
https://www.ncbi.nlm.nih.gov/pubmed/23737793
http://dx.doi.org/10.1155/2013/848021
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author Bissada, Eric
Abboud, Olivier
Abou Chacra, Zahi
Guertin, Louis
Weng, Xiaoduan
Nguyen-Tan, Phuc Félix
Tabet, Jean-Claude
Thibaudeau, Ève
Lambert, Louise
Audet, Marie-Lise
Fortin, Bernard
Soulières, Denis
author_facet Bissada, Eric
Abboud, Olivier
Abou Chacra, Zahi
Guertin, Louis
Weng, Xiaoduan
Nguyen-Tan, Phuc Félix
Tabet, Jean-Claude
Thibaudeau, Ève
Lambert, Louise
Audet, Marie-Lise
Fortin, Bernard
Soulières, Denis
author_sort Bissada, Eric
collection PubMed
description Background. RAS gene mutations have an impact on treatment response and overall prognosis for certain types of cancer. Objectives. To determine the prevalence and impact of K-RAS codons 12 and 13 mutations in patients with locally advanced HNSCC treated with primary or adjuvant chemo-radiation. Methods. 428 consecutive patients were treated with chemo-radiation therapy and followed for a median of 37 months. From these, 199 paraffin embedded biopsy or surgical specimens were retrieved. DNA was isolated and analyzed for K-RAS mutational status. Results. DNA extraction was successful in 197 samples. Of the 197 specimens, 3.5% presented K-RAS codon 12 mutations. For mutated cases and non-mutated cases, complete initial response to chemoradiation therapy was 71 and 73% (P = 0.32). LRC was respectively 32 and 83% (P = 0.03), DFS was 27 and 68% (P = 0.12), distant metastasis-free survival was 100 and 81% (P = 0.30) and OS was 57 and 65% (P = 0.14) at three years. K-Ras codon 13 analysis revealed no mutation. Conclusion. K-RAS codon 12 mutational status, although not associated with a difference in response rate, may influence the failure pattern and the type of therapy offered to patients with HNSCC. Our study did not reveal any mutation of K-RAS codon 13.
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spelling pubmed-36574502013-06-04 Prevalence of K-RAS Codons 12 and 13 Mutations in Locally Advanced Head and Neck Squamous Cell Carcinoma and Impact on Clinical Outcomes Bissada, Eric Abboud, Olivier Abou Chacra, Zahi Guertin, Louis Weng, Xiaoduan Nguyen-Tan, Phuc Félix Tabet, Jean-Claude Thibaudeau, Ève Lambert, Louise Audet, Marie-Lise Fortin, Bernard Soulières, Denis Int J Otolaryngol Clinical Study Background. RAS gene mutations have an impact on treatment response and overall prognosis for certain types of cancer. Objectives. To determine the prevalence and impact of K-RAS codons 12 and 13 mutations in patients with locally advanced HNSCC treated with primary or adjuvant chemo-radiation. Methods. 428 consecutive patients were treated with chemo-radiation therapy and followed for a median of 37 months. From these, 199 paraffin embedded biopsy or surgical specimens were retrieved. DNA was isolated and analyzed for K-RAS mutational status. Results. DNA extraction was successful in 197 samples. Of the 197 specimens, 3.5% presented K-RAS codon 12 mutations. For mutated cases and non-mutated cases, complete initial response to chemoradiation therapy was 71 and 73% (P = 0.32). LRC was respectively 32 and 83% (P = 0.03), DFS was 27 and 68% (P = 0.12), distant metastasis-free survival was 100 and 81% (P = 0.30) and OS was 57 and 65% (P = 0.14) at three years. K-Ras codon 13 analysis revealed no mutation. Conclusion. K-RAS codon 12 mutational status, although not associated with a difference in response rate, may influence the failure pattern and the type of therapy offered to patients with HNSCC. Our study did not reveal any mutation of K-RAS codon 13. Hindawi Publishing Corporation 2013 2013-04-30 /pmc/articles/PMC3657450/ /pubmed/23737793 http://dx.doi.org/10.1155/2013/848021 Text en Copyright © 2013 Eric Bissada et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Bissada, Eric
Abboud, Olivier
Abou Chacra, Zahi
Guertin, Louis
Weng, Xiaoduan
Nguyen-Tan, Phuc Félix
Tabet, Jean-Claude
Thibaudeau, Ève
Lambert, Louise
Audet, Marie-Lise
Fortin, Bernard
Soulières, Denis
Prevalence of K-RAS Codons 12 and 13 Mutations in Locally Advanced Head and Neck Squamous Cell Carcinoma and Impact on Clinical Outcomes
title Prevalence of K-RAS Codons 12 and 13 Mutations in Locally Advanced Head and Neck Squamous Cell Carcinoma and Impact on Clinical Outcomes
title_full Prevalence of K-RAS Codons 12 and 13 Mutations in Locally Advanced Head and Neck Squamous Cell Carcinoma and Impact on Clinical Outcomes
title_fullStr Prevalence of K-RAS Codons 12 and 13 Mutations in Locally Advanced Head and Neck Squamous Cell Carcinoma and Impact on Clinical Outcomes
title_full_unstemmed Prevalence of K-RAS Codons 12 and 13 Mutations in Locally Advanced Head and Neck Squamous Cell Carcinoma and Impact on Clinical Outcomes
title_short Prevalence of K-RAS Codons 12 and 13 Mutations in Locally Advanced Head and Neck Squamous Cell Carcinoma and Impact on Clinical Outcomes
title_sort prevalence of k-ras codons 12 and 13 mutations in locally advanced head and neck squamous cell carcinoma and impact on clinical outcomes
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3657450/
https://www.ncbi.nlm.nih.gov/pubmed/23737793
http://dx.doi.org/10.1155/2013/848021
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