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Circulating tumor DNA for personalized lung cancer monitoring

Advances in deep sequencing technology have led to developments in personalized medicine. Here, we describe the implications of a recent investigation that sequenced ctDNA from the plasma of non-small cell lung cancer patients to develop personalized ctDNA tests. These ‘liquid biopsies’ have shown p...

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Detalles Bibliográficos
Autores principales: Fiala, Clare, Diamandis, Eleftherios P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559853/
https://www.ncbi.nlm.nih.gov/pubmed/28814291
http://dx.doi.org/10.1186/s12916-017-0921-6
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author Fiala, Clare
Diamandis, Eleftherios P.
author_facet Fiala, Clare
Diamandis, Eleftherios P.
author_sort Fiala, Clare
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description Advances in deep sequencing technology have led to developments in personalized medicine. Here, we describe the implications of a recent investigation that sequenced ctDNA from the plasma of non-small cell lung cancer patients to develop personalized ctDNA tests. These ‘liquid biopsies’ have shown promise in monitoring tumor growth and response to treatment, providing a timely overview of mutations present in the tumor. We discuss the advantages of this budding approach, as well as its challenges and drawbacks, while also providing areas for further investigation and an outlook for the future.
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spelling pubmed-55598532017-08-18 Circulating tumor DNA for personalized lung cancer monitoring Fiala, Clare Diamandis, Eleftherios P. BMC Med Commentary Advances in deep sequencing technology have led to developments in personalized medicine. Here, we describe the implications of a recent investigation that sequenced ctDNA from the plasma of non-small cell lung cancer patients to develop personalized ctDNA tests. These ‘liquid biopsies’ have shown promise in monitoring tumor growth and response to treatment, providing a timely overview of mutations present in the tumor. We discuss the advantages of this budding approach, as well as its challenges and drawbacks, while also providing areas for further investigation and an outlook for the future. BioMed Central 2017-08-17 /pmc/articles/PMC5559853/ /pubmed/28814291 http://dx.doi.org/10.1186/s12916-017-0921-6 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Commentary
Fiala, Clare
Diamandis, Eleftherios P.
Circulating tumor DNA for personalized lung cancer monitoring
title Circulating tumor DNA for personalized lung cancer monitoring
title_full Circulating tumor DNA for personalized lung cancer monitoring
title_fullStr Circulating tumor DNA for personalized lung cancer monitoring
title_full_unstemmed Circulating tumor DNA for personalized lung cancer monitoring
title_short Circulating tumor DNA for personalized lung cancer monitoring
title_sort circulating tumor dna for personalized lung cancer monitoring
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559853/
https://www.ncbi.nlm.nih.gov/pubmed/28814291
http://dx.doi.org/10.1186/s12916-017-0921-6
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