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Advanced Pancreatic Ductal Adenocarcinoma: Moving Forward
Globally, the death rate of pancreatic ductal adenocarcinoma (PDAC) has doubled over 30 years and is likely to further increase, making PDAC a leading cause of cancer-related death in the coming years. PDAC is typically diagnosed at an advanced stage, and modified FOLFIRINOX or nab-paclitaxel and ge...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409054/ https://www.ncbi.nlm.nih.gov/pubmed/32708493 http://dx.doi.org/10.3390/cancers12071955 |
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author | Franck, Caspar Müller, Christian Rosania, Rosa Croner, Roland S. Pech, Maciej Venerito, Marino |
author_facet | Franck, Caspar Müller, Christian Rosania, Rosa Croner, Roland S. Pech, Maciej Venerito, Marino |
author_sort | Franck, Caspar |
collection | PubMed |
description | Globally, the death rate of pancreatic ductal adenocarcinoma (PDAC) has doubled over 30 years and is likely to further increase, making PDAC a leading cause of cancer-related death in the coming years. PDAC is typically diagnosed at an advanced stage, and modified FOLFIRINOX or nab-paclitaxel and gemcitabine are the mainstay of systemic therapy. For elderly patients with good performance status, low-dose treatment can preserve quality of life without compromising cancer control or survival. Maintenance therapy should be considered in PDAC patients achieving disease control with systemic therapy. In particular, olaparib has demonstrated a progression-free survival benefit of 3.6 months in a subgroup of PDAC patients with germline BRCA1/2 mutations (ca. 10% of all PDAC). Pancreatic enzyme replacement therapy is often omitted in the treatment of patients with PDAC, with possibly deleterious consequences. Small intestinal bacterial overgrowth is highly prevalent in patients with PDAC and should be considered in the diagnostic algorithm of PDAC patients with bloating and diarrhea. Rivaroxaban has been associated with a reduced risk of thrombosis without an increase in major bleeding events, and its use should be considered in every patient with advanced PDAC undergoing systemic therapy. |
format | Online Article Text |
id | pubmed-7409054 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74090542020-08-26 Advanced Pancreatic Ductal Adenocarcinoma: Moving Forward Franck, Caspar Müller, Christian Rosania, Rosa Croner, Roland S. Pech, Maciej Venerito, Marino Cancers (Basel) Review Globally, the death rate of pancreatic ductal adenocarcinoma (PDAC) has doubled over 30 years and is likely to further increase, making PDAC a leading cause of cancer-related death in the coming years. PDAC is typically diagnosed at an advanced stage, and modified FOLFIRINOX or nab-paclitaxel and gemcitabine are the mainstay of systemic therapy. For elderly patients with good performance status, low-dose treatment can preserve quality of life without compromising cancer control or survival. Maintenance therapy should be considered in PDAC patients achieving disease control with systemic therapy. In particular, olaparib has demonstrated a progression-free survival benefit of 3.6 months in a subgroup of PDAC patients with germline BRCA1/2 mutations (ca. 10% of all PDAC). Pancreatic enzyme replacement therapy is often omitted in the treatment of patients with PDAC, with possibly deleterious consequences. Small intestinal bacterial overgrowth is highly prevalent in patients with PDAC and should be considered in the diagnostic algorithm of PDAC patients with bloating and diarrhea. Rivaroxaban has been associated with a reduced risk of thrombosis without an increase in major bleeding events, and its use should be considered in every patient with advanced PDAC undergoing systemic therapy. MDPI 2020-07-18 /pmc/articles/PMC7409054/ /pubmed/32708493 http://dx.doi.org/10.3390/cancers12071955 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Franck, Caspar Müller, Christian Rosania, Rosa Croner, Roland S. Pech, Maciej Venerito, Marino Advanced Pancreatic Ductal Adenocarcinoma: Moving Forward |
title | Advanced Pancreatic Ductal Adenocarcinoma: Moving Forward |
title_full | Advanced Pancreatic Ductal Adenocarcinoma: Moving Forward |
title_fullStr | Advanced Pancreatic Ductal Adenocarcinoma: Moving Forward |
title_full_unstemmed | Advanced Pancreatic Ductal Adenocarcinoma: Moving Forward |
title_short | Advanced Pancreatic Ductal Adenocarcinoma: Moving Forward |
title_sort | advanced pancreatic ductal adenocarcinoma: moving forward |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409054/ https://www.ncbi.nlm.nih.gov/pubmed/32708493 http://dx.doi.org/10.3390/cancers12071955 |
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