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Plasma Circulating Tumor DNA Levels for the Monitoring of Melanoma Patients: Landscape of Available Technologies and Clinical Applications

Melanoma is a cutaneous cancer with an increasing worldwide prevalence and high mortality due to unresectable or metastatic stages. Mutations in BRAF, NRAS, or KIT are present in more than 60% of melanoma cases, but a useful blood-based biomarker for the clinical monitoring of melanoma patients is s...

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Autores principales: Busser, Benoit, Lupo, Julien, Sancey, Lucie, Mouret, Stéphane, Faure, Patrice, Plumas, Joel, Chaperot, Laurence, Leccia, Marie Thérèse, Coll, Jean Luc, Hurbin, Amandine, Hainaut, Pierre, Charles, Julie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5397613/
https://www.ncbi.nlm.nih.gov/pubmed/28484715
http://dx.doi.org/10.1155/2017/5986129
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author Busser, Benoit
Lupo, Julien
Sancey, Lucie
Mouret, Stéphane
Faure, Patrice
Plumas, Joel
Chaperot, Laurence
Leccia, Marie Thérèse
Coll, Jean Luc
Hurbin, Amandine
Hainaut, Pierre
Charles, Julie
author_facet Busser, Benoit
Lupo, Julien
Sancey, Lucie
Mouret, Stéphane
Faure, Patrice
Plumas, Joel
Chaperot, Laurence
Leccia, Marie Thérèse
Coll, Jean Luc
Hurbin, Amandine
Hainaut, Pierre
Charles, Julie
author_sort Busser, Benoit
collection PubMed
description Melanoma is a cutaneous cancer with an increasing worldwide prevalence and high mortality due to unresectable or metastatic stages. Mutations in BRAF, NRAS, or KIT are present in more than 60% of melanoma cases, but a useful blood-based biomarker for the clinical monitoring of melanoma patients is still lacking. Thus, the analysis of circulating tumor cells (CTCs) and/or cell-free circulating tumor DNA (ctDNA) analysis from blood (liquid biopsies) appears to be a promising noninvasive, repeatable, and systemic sampling tool for detecting and monitoring melanoma. Here, we review the molecular biology-based strategies used for ctDNA quantification in melanoma patients, as well as their main clinical applications. Droplet digital PCR (ddPCR) and next generation sequencing (NGS) technologies appear to be two versatile and complementary strategies to study rare variant mutations for the detection and monitoring of melanoma progression. Among the different clinical uses of ctDNA, we highlight the assessment of molecular heterogeneity and the identification of genetic determinants for targeted therapy as well as the analysis of acquired resistance. Importantly, ctDNA quantification might also be a novel biomarker with a prognostic value for melanoma patients.
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spelling pubmed-53976132017-05-08 Plasma Circulating Tumor DNA Levels for the Monitoring of Melanoma Patients: Landscape of Available Technologies and Clinical Applications Busser, Benoit Lupo, Julien Sancey, Lucie Mouret, Stéphane Faure, Patrice Plumas, Joel Chaperot, Laurence Leccia, Marie Thérèse Coll, Jean Luc Hurbin, Amandine Hainaut, Pierre Charles, Julie Biomed Res Int Review Article Melanoma is a cutaneous cancer with an increasing worldwide prevalence and high mortality due to unresectable or metastatic stages. Mutations in BRAF, NRAS, or KIT are present in more than 60% of melanoma cases, but a useful blood-based biomarker for the clinical monitoring of melanoma patients is still lacking. Thus, the analysis of circulating tumor cells (CTCs) and/or cell-free circulating tumor DNA (ctDNA) analysis from blood (liquid biopsies) appears to be a promising noninvasive, repeatable, and systemic sampling tool for detecting and monitoring melanoma. Here, we review the molecular biology-based strategies used for ctDNA quantification in melanoma patients, as well as their main clinical applications. Droplet digital PCR (ddPCR) and next generation sequencing (NGS) technologies appear to be two versatile and complementary strategies to study rare variant mutations for the detection and monitoring of melanoma progression. Among the different clinical uses of ctDNA, we highlight the assessment of molecular heterogeneity and the identification of genetic determinants for targeted therapy as well as the analysis of acquired resistance. Importantly, ctDNA quantification might also be a novel biomarker with a prognostic value for melanoma patients. Hindawi 2017 2017-04-06 /pmc/articles/PMC5397613/ /pubmed/28484715 http://dx.doi.org/10.1155/2017/5986129 Text en Copyright © 2017 Benoit Busser et al. https://creativecommons.org/licenses/by/4.0/ 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 Review Article
Busser, Benoit
Lupo, Julien
Sancey, Lucie
Mouret, Stéphane
Faure, Patrice
Plumas, Joel
Chaperot, Laurence
Leccia, Marie Thérèse
Coll, Jean Luc
Hurbin, Amandine
Hainaut, Pierre
Charles, Julie
Plasma Circulating Tumor DNA Levels for the Monitoring of Melanoma Patients: Landscape of Available Technologies and Clinical Applications
title Plasma Circulating Tumor DNA Levels for the Monitoring of Melanoma Patients: Landscape of Available Technologies and Clinical Applications
title_full Plasma Circulating Tumor DNA Levels for the Monitoring of Melanoma Patients: Landscape of Available Technologies and Clinical Applications
title_fullStr Plasma Circulating Tumor DNA Levels for the Monitoring of Melanoma Patients: Landscape of Available Technologies and Clinical Applications
title_full_unstemmed Plasma Circulating Tumor DNA Levels for the Monitoring of Melanoma Patients: Landscape of Available Technologies and Clinical Applications
title_short Plasma Circulating Tumor DNA Levels for the Monitoring of Melanoma Patients: Landscape of Available Technologies and Clinical Applications
title_sort plasma circulating tumor dna levels for the monitoring of melanoma patients: landscape of available technologies and clinical applications
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5397613/
https://www.ncbi.nlm.nih.gov/pubmed/28484715
http://dx.doi.org/10.1155/2017/5986129
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