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dc.contributor.authorRapado-González, Óscar
dc.contributor.authorBrea-Iglesias, Jenifer
dc.contributor.authorRodríguez-Casanova, Aitor
dc.contributor.authorBao-Caamano, Aida
dc.contributor.authorLópez-Cedrún, José-Luis
dc.contributor.authorTriana-Martínez, Gabriel
dc.contributor.authorDíaz-Peña, Roberto
dc.contributor.authorSantos, María Arminda
dc.contributor.authorLópez-López, Rafael
dc.contributor.authorMuinelo-Romay, Laura
dc.contributor.authorMartínez-Fernández, Mónica
dc.contributor.authorDíaz-Lagares, Ángel
dc.contributor.authorSuárez-Cunqueiro, María Mercedes
dc.date.accessioned2024-04-10T00:04:23Z
dc.date.available2024-04-10T00:04:23Z
dc.date.issued2023
dc.identifier10.1002/cam4.5436
dc.identifier.issn20457634
dc.identifier.urihttps://hdl.handle.net/20.500.12728/10378
dc.description.abstractBackground: We explore the utility of TruSight Tumor 170 panel (TST170) for detecting somatic mutations in tumor and cfDNA from locoregional recurrent and/or metastatic head and neck squamous cell carcinoma (HNSCC). Methods: Targeted NGS of tumor DNA and plasma cfDNA was performed using TST170 panel. In addition, a set of somatic mutations previously described in HNSCC were selected for validating in tumor, plasma, and saliva by digital droplet PCR. Results: The TST170 panel identified 13 non-synonymous somatic mutations, of which five were detected in tumoral tissue, other five in plasma cfDNA, and three in both tissue and plasma cfDNA. Of the eight somatic mutations identified in tissue, three were also identified in plasma cfDNA, showing an overall concordance rate of 37.5%. Conclusions: This preliminary study shows the possibility to detect somatic mutations in tumor and plasma of HNSCC patients using a single assay that would facilitate the clinical implementation of personalized medicine in the clinic. © 2022 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.es_ES
dc.description.sponsorshipAxudas do Programa de Consolidación e Estructuración de Unidades de Investigación Competitiva, (IN607A2020/02); Centro de Supercomputación de Galicia; Consellería de Economía, Emprego e Industria; Faculty of Science and Engineering, University of Manchester, FSE, (IN853B 2018/03); Federación Española de Enfermedades Raras, FEDER, (PI20/01449); Instituto de Salud Carlos III, ISCIII, (CP20/00129, FI19/00240, JR17/00016); European Social Fund, ESF; European Regional Development Fund, ERDF; Axencia Galega de Innovación, GAIN; Xunta de Galicia, (IN606B‐2022/007)es_ES
dc.language.isoenes_ES
dc.publisherJohn Wiley and Sons Inces_ES
dc.subjectcell-free DNAes_ES
dc.subjectdroplet digital PCRes_ES
dc.subjecthead and neck squamous cell carcinomaes_ES
dc.subjectliquid biopsyes_ES
dc.subjectnext-generation sequencinges_ES
dc.subjectsalivaes_ES
dc.subjectsomatic mutationses_ES
dc.titleSomatic mutations in tumor and plasma of locoregional recurrent and/or metastatic head and neck cancer using a next-generation sequencing panel: A preliminary studyes_ES
dc.typeArticlees_ES


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