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Systemic therapy in metastatic pancreatic adenocarcinoma: current practice and perspectives
Major breakthroughs have been achieved in the management of metastatic pancreatic ductal adenocarcinoma (PDAC) with FOLFIRINOX (5-fluorouracil + irinotecan + oxaliplatin) and gemcitabine plus nab-paclitaxel approved as a first-line therapy, although the prognosis is still poor. At progression, patie...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8264726/ https://www.ncbi.nlm.nih.gov/pubmed/34285720 http://dx.doi.org/10.1177/17588359211018539 |
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author | Lellouche, Lisa Palmieri, Lola-Jade Dermine, Solène Brezault, Catherine Chaussade, Stanislas Coriat, Romain |
author_facet | Lellouche, Lisa Palmieri, Lola-Jade Dermine, Solène Brezault, Catherine Chaussade, Stanislas Coriat, Romain |
author_sort | Lellouche, Lisa |
collection | PubMed |
description | Major breakthroughs have been achieved in the management of metastatic pancreatic ductal adenocarcinoma (PDAC) with FOLFIRINOX (5-fluorouracil + irinotecan + oxaliplatin) and gemcitabine plus nab-paclitaxel approved as a first-line therapy, although the prognosis is still poor. At progression, patients who maintain a good performance status (PS) can benefit from second-line chemotherapy. To address the concern of achieving tumor control while maintaining a good quality of life, maintenance therapy is a concept that has now emerged. After a FOLFIRINOX induction treatment, maintenance with 5-fluorouracil (5-FU) seems to offer a promising approach. Although not confirmed in large, prospective trials, gemcitabine alone as a maintenance therapy following induction treatment with gemcitabine plus nab-paclitaxel could be an option, while a small subset of patients with a germline mutation of breast cancer gene (BRCA) can benefit from the polyadenosine diphosphate-ribose polymerase (PARP) inhibitor olaparib. The rate of PDAC with molecular alterations that could lead to a specific therapy is up to 25%. The Food and Drug Administration (FDA) recently approved larotrectinib for patients with any tumors harboring a neurotrophic tyrosine receptor kinase (NTRK) gene fusion, and pembrolizumab for patients with a mismatch repair deficiency in a second-line setting, including PDAC. Research focused on targeted therapy and immunotherapy is active and could improve patients’ outcomes in the near future. |
format | Online Article Text |
id | pubmed-8264726 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-82647262021-07-19 Systemic therapy in metastatic pancreatic adenocarcinoma: current practice and perspectives Lellouche, Lisa Palmieri, Lola-Jade Dermine, Solène Brezault, Catherine Chaussade, Stanislas Coriat, Romain Ther Adv Med Oncol Advances in Treatment of Lung Cancer Patients with Targetable Mutations Major breakthroughs have been achieved in the management of metastatic pancreatic ductal adenocarcinoma (PDAC) with FOLFIRINOX (5-fluorouracil + irinotecan + oxaliplatin) and gemcitabine plus nab-paclitaxel approved as a first-line therapy, although the prognosis is still poor. At progression, patients who maintain a good performance status (PS) can benefit from second-line chemotherapy. To address the concern of achieving tumor control while maintaining a good quality of life, maintenance therapy is a concept that has now emerged. After a FOLFIRINOX induction treatment, maintenance with 5-fluorouracil (5-FU) seems to offer a promising approach. Although not confirmed in large, prospective trials, gemcitabine alone as a maintenance therapy following induction treatment with gemcitabine plus nab-paclitaxel could be an option, while a small subset of patients with a germline mutation of breast cancer gene (BRCA) can benefit from the polyadenosine diphosphate-ribose polymerase (PARP) inhibitor olaparib. The rate of PDAC with molecular alterations that could lead to a specific therapy is up to 25%. The Food and Drug Administration (FDA) recently approved larotrectinib for patients with any tumors harboring a neurotrophic tyrosine receptor kinase (NTRK) gene fusion, and pembrolizumab for patients with a mismatch repair deficiency in a second-line setting, including PDAC. Research focused on targeted therapy and immunotherapy is active and could improve patients’ outcomes in the near future. SAGE Publications 2021-07-06 /pmc/articles/PMC8264726/ /pubmed/34285720 http://dx.doi.org/10.1177/17588359211018539 Text en © The Author(s), 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Advances in Treatment of Lung Cancer Patients with Targetable Mutations Lellouche, Lisa Palmieri, Lola-Jade Dermine, Solène Brezault, Catherine Chaussade, Stanislas Coriat, Romain Systemic therapy in metastatic pancreatic adenocarcinoma: current practice and perspectives |
title | Systemic therapy in metastatic pancreatic adenocarcinoma: current practice and perspectives |
title_full | Systemic therapy in metastatic pancreatic adenocarcinoma: current practice and perspectives |
title_fullStr | Systemic therapy in metastatic pancreatic adenocarcinoma: current practice and perspectives |
title_full_unstemmed | Systemic therapy in metastatic pancreatic adenocarcinoma: current practice and perspectives |
title_short | Systemic therapy in metastatic pancreatic adenocarcinoma: current practice and perspectives |
title_sort | systemic therapy in metastatic pancreatic adenocarcinoma: current practice and perspectives |
topic | Advances in Treatment of Lung Cancer Patients with Targetable Mutations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8264726/ https://www.ncbi.nlm.nih.gov/pubmed/34285720 http://dx.doi.org/10.1177/17588359211018539 |
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