Impact of genetic variants in clinical outcome of a cohort of patients with oropharyngeal squamous cell carcinoma

Tobacco- or human papillomavirus- driven oropharyngeal squamous cell carcinomas (OpSCC) represent distinct clinical, biological and epidemiological entities. The aim of this study was to identify genetic variants based on somatic alterations in OpSCC samples from an admixed population, and to test f...

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Autores:
de Carvalho, Ana Carolina
Perdomo Lara, Sandra Janneth
Dos Santos, Wellington
Carvalho Fernandes, Gabriela
Machado de Jesus, Lais
Santos Carvalho, Raiany
Scapulatempo-Neto, Cristovam
Caravina de Almeida, Gisele
Pereira Sorroche, Bruna
Rebolho Batista Arantes, Lidia Maria
Melendez, Matias Eliseo
De Marchi, Pedro
Hayes, Neil
Reis, Rui Manuel
Lopes Carvalho, André
Tipo de recurso:
Article of journal
Fecha de publicación:
2020
Institución:
Universidad El Bosque
Repositorio:
Repositorio U. El Bosque
Idioma:
eng
OAI Identifier:
oai:repositorio.unbosque.edu.co:20.500.12495/5257
Acceso en línea:
http://hdl.handle.net/20.500.12495/5257
https://doi.org/10.1038/s41598-020-66741-z
https://repositorio.unbosque.edu.co
Palabra clave:
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openAccess
License
Attribution-NonCommercial-NoDerivatives 4.0 International
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dc.title.spa.fl_str_mv Impact of genetic variants in clinical outcome of a cohort of patients with oropharyngeal squamous cell carcinoma
dc.title.translated.spa.fl_str_mv Impact of genetic variants in clinical outcome of a cohort of patients with oropharyngeal squamous cell carcinoma
title Impact of genetic variants in clinical outcome of a cohort of patients with oropharyngeal squamous cell carcinoma
spellingShingle Impact of genetic variants in clinical outcome of a cohort of patients with oropharyngeal squamous cell carcinoma
title_short Impact of genetic variants in clinical outcome of a cohort of patients with oropharyngeal squamous cell carcinoma
title_full Impact of genetic variants in clinical outcome of a cohort of patients with oropharyngeal squamous cell carcinoma
title_fullStr Impact of genetic variants in clinical outcome of a cohort of patients with oropharyngeal squamous cell carcinoma
title_full_unstemmed Impact of genetic variants in clinical outcome of a cohort of patients with oropharyngeal squamous cell carcinoma
title_sort Impact of genetic variants in clinical outcome of a cohort of patients with oropharyngeal squamous cell carcinoma
dc.creator.fl_str_mv de Carvalho, Ana Carolina
Perdomo Lara, Sandra Janneth
Dos Santos, Wellington
Carvalho Fernandes, Gabriela
Machado de Jesus, Lais
Santos Carvalho, Raiany
Scapulatempo-Neto, Cristovam
Caravina de Almeida, Gisele
Pereira Sorroche, Bruna
Rebolho Batista Arantes, Lidia Maria
Melendez, Matias Eliseo
De Marchi, Pedro
Hayes, Neil
Reis, Rui Manuel
Lopes Carvalho, André
dc.contributor.author.none.fl_str_mv de Carvalho, Ana Carolina
Perdomo Lara, Sandra Janneth
Dos Santos, Wellington
Carvalho Fernandes, Gabriela
Machado de Jesus, Lais
Santos Carvalho, Raiany
Scapulatempo-Neto, Cristovam
Caravina de Almeida, Gisele
Pereira Sorroche, Bruna
Rebolho Batista Arantes, Lidia Maria
Melendez, Matias Eliseo
De Marchi, Pedro
Hayes, Neil
Reis, Rui Manuel
Lopes Carvalho, André
dc.contributor.orcid.none.fl_str_mv Perdomo Lara, Sandra Janneth [0000-0002-4429-3760]
description Tobacco- or human papillomavirus- driven oropharyngeal squamous cell carcinomas (OpSCC) represent distinct clinical, biological and epidemiological entities. The aim of this study was to identify genetic variants based on somatic alterations in OpSCC samples from an admixed population, and to test for association with clinical features. The entire coding region of 15 OpSCC driver genes was sequenced by next-generation sequencing in 51 OpSCC FFPE samples. Thirty-five percent of the patients (18/51) were HPV-positive and current or past tobacco consumption was reported in 86.3% (44/51). The mutation profile identified an average of 2.67 variants per sample. Sixty-three percent of patients (32/51; 62.7%) were mutated for at least one of the genes tested and TP53 was the most frequently mutated gene. The presence of mutation in NOTCH1 and PTEN, significantly decreased patient's recurrence-free survival, but only NOTCH1 mutation remained significant after stepwise selection, with a risk of recurrence of 4.5 (HR 95% CI = 1.11-14.57; Cox Regression p = 0.034). These results show that Brazilian OpSCC patients exhibit a similar clinical and genetic profile in comparison to other populations. Molecular characterization is a promising tool for the definition of clinical subgroups, aiding in a more precise tailoring of treatment and prognostication.
publishDate 2020
dc.date.issued.none.fl_str_mv 2020
dc.date.accessioned.none.fl_str_mv 2021-02-05T16:56:28Z
dc.date.available.none.fl_str_mv 2021-02-05T16:56:28Z
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dc.type.local.none.fl_str_mv Artículo de revista
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dc.identifier.issn.none.fl_str_mv 2045-2322
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dc.identifier.doi.none.fl_str_mv https://doi.org/10.1038/s41598-020-66741-z
dc.identifier.instname.spa.fl_str_mv instname:Universidad El Bosque
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url http://hdl.handle.net/20.500.12495/5257
https://doi.org/10.1038/s41598-020-66741-z
https://repositorio.unbosque.edu.co
dc.language.iso.none.fl_str_mv eng
language eng
dc.relation.ispartofseries.spa.fl_str_mv Scientific Reports, 2045-2322, Vol. 10, No. 1, 2020, p. 9970
dc.relation.uri.none.fl_str_mv https://www.nature.com/articles/s41598-020-66741-z
dc.rights.*.fl_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.uri.*.fl_str_mv http://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights.local.spa.fl_str_mv Acceso abierto
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Acceso abierto
dc.rights.creativecommons.none.fl_str_mv 2020-06-19
rights_invalid_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
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eu_rights_str_mv openAccess
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dc.publisher.spa.fl_str_mv Nature
dc.publisher.journal.spa.fl_str_mv Scientific Reports
institution Universidad El Bosque
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spelling de Carvalho, Ana CarolinaPerdomo Lara, Sandra JannethDos Santos, WellingtonCarvalho Fernandes, GabrielaMachado de Jesus, LaisSantos Carvalho, RaianyScapulatempo-Neto, CristovamCaravina de Almeida, GiselePereira Sorroche, BrunaRebolho Batista Arantes, Lidia MariaMelendez, Matias EliseoDe Marchi, PedroHayes, NeilReis, Rui ManuelLopes Carvalho, AndréPerdomo Lara, Sandra Janneth [0000-0002-4429-3760]2021-02-05T16:56:28Z2021-02-05T16:56:28Z20202045-2322http://hdl.handle.net/20.500.12495/5257https://doi.org/10.1038/s41598-020-66741-zinstname:Universidad El Bosquereponame:Repositorio Institucional Universidad El Bosquehttps://repositorio.unbosque.edu.coapplication/pdfengNatureScientific ReportsScientific Reports, 2045-2322, Vol. 10, No. 1, 2020, p. 9970https://www.nature.com/articles/s41598-020-66741-zAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/Acceso abiertohttp://purl.org/coar/access_right/c_abf2info:eu-repo/semantics/openAccessAcceso abierto2020-06-19Impact of genetic variants in clinical outcome of a cohort of patients with oropharyngeal squamous cell carcinomaImpact of genetic variants in clinical outcome of a cohort of patients with oropharyngeal squamous cell carcinomaArtículo de revistahttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1info:eu-repo/semantics/articlehttp://purl.org/coar/version/c_970fb48d4fbd8a85Tobacco- or human papillomavirus- driven oropharyngeal squamous cell carcinomas (OpSCC) represent distinct clinical, biological and epidemiological entities. The aim of this study was to identify genetic variants based on somatic alterations in OpSCC samples from an admixed population, and to test for association with clinical features. The entire coding region of 15 OpSCC driver genes was sequenced by next-generation sequencing in 51 OpSCC FFPE samples. Thirty-five percent of the patients (18/51) were HPV-positive and current or past tobacco consumption was reported in 86.3% (44/51). The mutation profile identified an average of 2.67 variants per sample. Sixty-three percent of patients (32/51; 62.7%) were mutated for at least one of the genes tested and TP53 was the most frequently mutated gene. The presence of mutation in NOTCH1 and PTEN, significantly decreased patient's recurrence-free survival, but only NOTCH1 mutation remained significant after stepwise selection, with a risk of recurrence of 4.5 (HR 95% CI = 1.11-14.57; Cox Regression p = 0.034). These results show that Brazilian OpSCC patients exhibit a similar clinical and genetic profile in comparison to other populations. 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