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Biomarkers in pancreatic adenocarcinoma: current perspectives

Pancreatic ductal adenocarcinoma (PDAC) has a poor prognosis, with a 5-year survival rate of 7.7%. Most patients are diagnosed at an advanced stage not amenable to potentially curative resection. A substantial portion of this review is dedicated to reviewing the current literature on carbohydrate an...

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Autores principales: Swords, Douglas S, Firpo, Matthew A, Scaife, Courtney L, Mulvihill, Sean J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5158171/
https://www.ncbi.nlm.nih.gov/pubmed/28003762
http://dx.doi.org/10.2147/OTT.S100510
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author Swords, Douglas S
Firpo, Matthew A
Scaife, Courtney L
Mulvihill, Sean J
author_facet Swords, Douglas S
Firpo, Matthew A
Scaife, Courtney L
Mulvihill, Sean J
author_sort Swords, Douglas S
collection PubMed
description Pancreatic ductal adenocarcinoma (PDAC) has a poor prognosis, with a 5-year survival rate of 7.7%. Most patients are diagnosed at an advanced stage not amenable to potentially curative resection. A substantial portion of this review is dedicated to reviewing the current literature on carbohydrate antigen (CA 19-9), which is currently the only guideline-recommended biomarker for PDAC. It provides valuable prognostic information, can predict resectability, and is useful in decision making about neoadjuvant therapy. We also discuss carcinoembryonic antigen (CEA), CA 125, serum biomarker panels, circulating tumor cells, and cell-free nucleic acids. Although many biomarkers have now been studied in relation to PDAC, significant work still needs to be done to validate their usefulness in the early detection of PDAC and management of patients with PDAC.
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spelling pubmed-51581712016-12-21 Biomarkers in pancreatic adenocarcinoma: current perspectives Swords, Douglas S Firpo, Matthew A Scaife, Courtney L Mulvihill, Sean J Onco Targets Ther Review Pancreatic ductal adenocarcinoma (PDAC) has a poor prognosis, with a 5-year survival rate of 7.7%. Most patients are diagnosed at an advanced stage not amenable to potentially curative resection. A substantial portion of this review is dedicated to reviewing the current literature on carbohydrate antigen (CA 19-9), which is currently the only guideline-recommended biomarker for PDAC. It provides valuable prognostic information, can predict resectability, and is useful in decision making about neoadjuvant therapy. We also discuss carcinoembryonic antigen (CEA), CA 125, serum biomarker panels, circulating tumor cells, and cell-free nucleic acids. Although many biomarkers have now been studied in relation to PDAC, significant work still needs to be done to validate their usefulness in the early detection of PDAC and management of patients with PDAC. Dove Medical Press 2016-12-09 /pmc/articles/PMC5158171/ /pubmed/28003762 http://dx.doi.org/10.2147/OTT.S100510 Text en © 2016 Swords et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Swords, Douglas S
Firpo, Matthew A
Scaife, Courtney L
Mulvihill, Sean J
Biomarkers in pancreatic adenocarcinoma: current perspectives
title Biomarkers in pancreatic adenocarcinoma: current perspectives
title_full Biomarkers in pancreatic adenocarcinoma: current perspectives
title_fullStr Biomarkers in pancreatic adenocarcinoma: current perspectives
title_full_unstemmed Biomarkers in pancreatic adenocarcinoma: current perspectives
title_short Biomarkers in pancreatic adenocarcinoma: current perspectives
title_sort biomarkers in pancreatic adenocarcinoma: current perspectives
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5158171/
https://www.ncbi.nlm.nih.gov/pubmed/28003762
http://dx.doi.org/10.2147/OTT.S100510
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