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Locoregional therapies and their effects on the tumoral microenvironment of pancreatic ductal adenocarcinoma

Pancreatic ductal adenocarcinoma (PDAC) is expected to become the second leading cause of death from cancer by 2030. Despite intensive research in the field of therapeutics, the 5-year overall survival is approximately 8%, with only 20% of patients eligible for surgery at the time of diagnosis. The...

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Autores principales: Lambin, Thomas, Lafon, Cyril, Drainville, Robert Andrew, Pioche, Mathieu, Prat, Frédéric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9099187/
https://www.ncbi.nlm.nih.gov/pubmed/35645539
http://dx.doi.org/10.3748/wjg.v28.i13.1288
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author Lambin, Thomas
Lafon, Cyril
Drainville, Robert Andrew
Pioche, Mathieu
Prat, Frédéric
author_facet Lambin, Thomas
Lafon, Cyril
Drainville, Robert Andrew
Pioche, Mathieu
Prat, Frédéric
author_sort Lambin, Thomas
collection PubMed
description Pancreatic ductal adenocarcinoma (PDAC) is expected to become the second leading cause of death from cancer by 2030. Despite intensive research in the field of therapeutics, the 5-year overall survival is approximately 8%, with only 20% of patients eligible for surgery at the time of diagnosis. The tumoral microenvironment (TME) of the PDAC is one of the main causes for resistance to antitumoral treatments due to the presence of tumor vasculature, stroma, and a modified immune response. The TME of PDAC is characterized by high stiffness due to fibrosis, with hypo microvascular perfusion, along with an immunosuppressive environment that constitutes a barrier to effective antitumoral treatment. While systemic therapies often produce severe side effects that can alter patients’ quality of life, locoregional therapies have gained attention since their action is localized to the pancreas and can thus alleviate some of the barriers to effective antitumoral treatment due to their physical effects. Local hyperthermia using radiofrequency ablation and radiation therapy - most commonly using a local high single dose - are the two main modalities holding promise for clinical efficacy. Recently, irreversible electroporation and focused ultrasound-derived cavitation have gained increasing attention. To date, most of the data are limited to preclinical studies, but ongoing clinical trials may help better define the role of these locoregional therapies in the management of PDAC patients.
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spelling pubmed-90991872022-05-26 Locoregional therapies and their effects on the tumoral microenvironment of pancreatic ductal adenocarcinoma Lambin, Thomas Lafon, Cyril Drainville, Robert Andrew Pioche, Mathieu Prat, Frédéric World J Gastroenterol Review Pancreatic ductal adenocarcinoma (PDAC) is expected to become the second leading cause of death from cancer by 2030. Despite intensive research in the field of therapeutics, the 5-year overall survival is approximately 8%, with only 20% of patients eligible for surgery at the time of diagnosis. The tumoral microenvironment (TME) of the PDAC is one of the main causes for resistance to antitumoral treatments due to the presence of tumor vasculature, stroma, and a modified immune response. The TME of PDAC is characterized by high stiffness due to fibrosis, with hypo microvascular perfusion, along with an immunosuppressive environment that constitutes a barrier to effective antitumoral treatment. While systemic therapies often produce severe side effects that can alter patients’ quality of life, locoregional therapies have gained attention since their action is localized to the pancreas and can thus alleviate some of the barriers to effective antitumoral treatment due to their physical effects. Local hyperthermia using radiofrequency ablation and radiation therapy - most commonly using a local high single dose - are the two main modalities holding promise for clinical efficacy. Recently, irreversible electroporation and focused ultrasound-derived cavitation have gained increasing attention. To date, most of the data are limited to preclinical studies, but ongoing clinical trials may help better define the role of these locoregional therapies in the management of PDAC patients. Baishideng Publishing Group Inc 2022-04-07 2022-04-07 /pmc/articles/PMC9099187/ /pubmed/35645539 http://dx.doi.org/10.3748/wjg.v28.i13.1288 Text en ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
spellingShingle Review
Lambin, Thomas
Lafon, Cyril
Drainville, Robert Andrew
Pioche, Mathieu
Prat, Frédéric
Locoregional therapies and their effects on the tumoral microenvironment of pancreatic ductal adenocarcinoma
title Locoregional therapies and their effects on the tumoral microenvironment of pancreatic ductal adenocarcinoma
title_full Locoregional therapies and their effects on the tumoral microenvironment of pancreatic ductal adenocarcinoma
title_fullStr Locoregional therapies and their effects on the tumoral microenvironment of pancreatic ductal adenocarcinoma
title_full_unstemmed Locoregional therapies and their effects on the tumoral microenvironment of pancreatic ductal adenocarcinoma
title_short Locoregional therapies and their effects on the tumoral microenvironment of pancreatic ductal adenocarcinoma
title_sort locoregional therapies and their effects on the tumoral microenvironment of pancreatic ductal adenocarcinoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9099187/
https://www.ncbi.nlm.nih.gov/pubmed/35645539
http://dx.doi.org/10.3748/wjg.v28.i13.1288
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