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Treatment Options for Germline BRCA-Mutated Metastatic Pancreatic Adenocarcinoma

Pancreatic cancer is the fourth leading cause of death from cancer in both men and women. Pancreatic cancer is typically diagnosed at an advanced stage and has an overall 5-year survival of approximately 9.3%. The National Comprehensive Cancer Network recommends both germline testing (testing cells...

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Autor principal: Grzelak, Doreen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Harborside Press LLC 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8299794/
https://www.ncbi.nlm.nih.gov/pubmed/34430059
http://dx.doi.org/10.6004/jadpro.2021.12.5.4
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author Grzelak, Doreen
author_facet Grzelak, Doreen
author_sort Grzelak, Doreen
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description Pancreatic cancer is the fourth leading cause of death from cancer in both men and women. Pancreatic cancer is typically diagnosed at an advanced stage and has an overall 5-year survival of approximately 9.3%. The National Comprehensive Cancer Network recommends both germline testing (testing cells such as blood or skin that do not have cancer) as well as somatic testing (testing cells with cancer) for pathogenic variants that may increase the risk of pancreatic cancer. In December 2019, the U.S. Food & Drug Administration approved the poly(ADP-ribose) polymerase (PARP) inhibitor olaparib for maintenance treatment of germline BRCA-mutated metastatic pancreatic adenocarcinoma in individuals who have completed at least 16 weeks of progression-free treatment with first-line platinum-based chemotherapy. This new therapy option has implications not only for treatment but also for the role of the oncology advanced practitioner as genetic testing becomes more prevalent in the care of patients with cancer.
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spelling pubmed-82997942021-08-23 Treatment Options for Germline BRCA-Mutated Metastatic Pancreatic Adenocarcinoma Grzelak, Doreen J Adv Pract Oncol Review Pancreatic cancer is the fourth leading cause of death from cancer in both men and women. Pancreatic cancer is typically diagnosed at an advanced stage and has an overall 5-year survival of approximately 9.3%. The National Comprehensive Cancer Network recommends both germline testing (testing cells such as blood or skin that do not have cancer) as well as somatic testing (testing cells with cancer) for pathogenic variants that may increase the risk of pancreatic cancer. In December 2019, the U.S. Food & Drug Administration approved the poly(ADP-ribose) polymerase (PARP) inhibitor olaparib for maintenance treatment of germline BRCA-mutated metastatic pancreatic adenocarcinoma in individuals who have completed at least 16 weeks of progression-free treatment with first-line platinum-based chemotherapy. This new therapy option has implications not only for treatment but also for the role of the oncology advanced practitioner as genetic testing becomes more prevalent in the care of patients with cancer. Harborside Press LLC 2021-07 2021-07-01 /pmc/articles/PMC8299794/ /pubmed/34430059 http://dx.doi.org/10.6004/jadpro.2021.12.5.4 Text en © 2021 Harborside™ https://creativecommons.org/licenses/by-nc-nd/3.0/This article is distributed under the terms of the Creative Commons Attribution Non-Commercial Non-Derivative License, which permits unrestricted non-commercial and non-derivative use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Grzelak, Doreen
Treatment Options for Germline BRCA-Mutated Metastatic Pancreatic Adenocarcinoma
title Treatment Options for Germline BRCA-Mutated Metastatic Pancreatic Adenocarcinoma
title_full Treatment Options for Germline BRCA-Mutated Metastatic Pancreatic Adenocarcinoma
title_fullStr Treatment Options for Germline BRCA-Mutated Metastatic Pancreatic Adenocarcinoma
title_full_unstemmed Treatment Options for Germline BRCA-Mutated Metastatic Pancreatic Adenocarcinoma
title_short Treatment Options for Germline BRCA-Mutated Metastatic Pancreatic Adenocarcinoma
title_sort treatment options for germline brca-mutated metastatic pancreatic adenocarcinoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8299794/
https://www.ncbi.nlm.nih.gov/pubmed/34430059
http://dx.doi.org/10.6004/jadpro.2021.12.5.4
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