Germline Variants in DNA Damage Repair Genes: An Emerging Role in the Era of Precision Medicine in Pancreatic Adenocarcinoma

Abstract Pancreatic adenocarcinoma is a lethal disease that is projected to become the second most common cause of cancer deaths by 2030. The role of adjuvant therapy after surgical resection has been established by several clinical trials to prolong survival and improve outcomes. Multiagent chemoth...

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Main Authors: Sami Shoucair, Andrew R. Baker, Jun Yu
Format: Article
Language:English
Published: Wiley 2022-01-01
Series:Annals of Gastroenterological Surgery
Subjects:
Online Access:https://doi.org/10.1002/ags3.12514
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author Sami Shoucair
Andrew R. Baker
Jun Yu
author_facet Sami Shoucair
Andrew R. Baker
Jun Yu
author_sort Sami Shoucair
collection DOAJ
description Abstract Pancreatic adenocarcinoma is a lethal disease that is projected to become the second most common cause of cancer deaths by 2030. The role of adjuvant therapy after surgical resection has been established by several clinical trials to prolong survival and improve outcomes. Multiagent chemotherapy seems to be the most promising approach to counteract early recurrence and improve survival; however, in the era of precision medicine, patient selection and individualized therapy seems to hold the key to desirable superior outcomes. Several cancer susceptibility genes have been proven to be associated with an increased risk of pancreatic cancer, both familial and sporadic cases. The role of genomic profiling for germline variants has been extensive and of limited clinical value, considering their low prevalence in pancreatic ductal adenocarcinoma (PDAC). However, an accumulating body of evidence from several studies in the past decade have successfully shown a recognizable value of germline variants in risk assessment and patient stratification. Recently, anti‐PD‐1 therapy (pembrolizumab) has been FDA‐approved for use in solid malignancies with a Mismatch repair deficiency or high Microsatellite instability. Several trials have evaluated the role of poly (ADP‐ribose) polymerase (PARP) inhibitors in patients harboring germline BRCA1/2 mutations. Finally, germline variants in DNA damage response genes and particularly deleterious ones have the potential to guide therapy after surgical resection and serve as biomarkers to predict survival. The dire need to address challenges for applying precision medicine in real‐life clinical settings for PDAC patients lies in further characterizing the genetic and molecular processes through translational research.
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spelling doaj.art-cff0cfdf4e09475ca5a5e6826810fdaf2022-12-22T04:10:18ZengWileyAnnals of Gastroenterological Surgery2475-03282022-01-016171610.1002/ags3.12514Germline Variants in DNA Damage Repair Genes: An Emerging Role in the Era of Precision Medicine in Pancreatic AdenocarcinomaSami Shoucair0Andrew R. Baker1Jun Yu2Department of Surgery Johns Hopkins University School of Medicine Baltimore MD USACellular and Molecular Medicine Graduate Program Johns Hopkins University School of Medicine Baltimore MD USADepartment of Surgery Johns Hopkins University School of Medicine Baltimore MD USAAbstract Pancreatic adenocarcinoma is a lethal disease that is projected to become the second most common cause of cancer deaths by 2030. The role of adjuvant therapy after surgical resection has been established by several clinical trials to prolong survival and improve outcomes. Multiagent chemotherapy seems to be the most promising approach to counteract early recurrence and improve survival; however, in the era of precision medicine, patient selection and individualized therapy seems to hold the key to desirable superior outcomes. Several cancer susceptibility genes have been proven to be associated with an increased risk of pancreatic cancer, both familial and sporadic cases. The role of genomic profiling for germline variants has been extensive and of limited clinical value, considering their low prevalence in pancreatic ductal adenocarcinoma (PDAC). However, an accumulating body of evidence from several studies in the past decade have successfully shown a recognizable value of germline variants in risk assessment and patient stratification. Recently, anti‐PD‐1 therapy (pembrolizumab) has been FDA‐approved for use in solid malignancies with a Mismatch repair deficiency or high Microsatellite instability. Several trials have evaluated the role of poly (ADP‐ribose) polymerase (PARP) inhibitors in patients harboring germline BRCA1/2 mutations. Finally, germline variants in DNA damage response genes and particularly deleterious ones have the potential to guide therapy after surgical resection and serve as biomarkers to predict survival. The dire need to address challenges for applying precision medicine in real‐life clinical settings for PDAC patients lies in further characterizing the genetic and molecular processes through translational research.https://doi.org/10.1002/ags3.12514DDR genesgermline variantspancreatic cancerprecision medicine
spellingShingle Sami Shoucair
Andrew R. Baker
Jun Yu
Germline Variants in DNA Damage Repair Genes: An Emerging Role in the Era of Precision Medicine in Pancreatic Adenocarcinoma
Annals of Gastroenterological Surgery
DDR genes
germline variants
pancreatic cancer
precision medicine
title Germline Variants in DNA Damage Repair Genes: An Emerging Role in the Era of Precision Medicine in Pancreatic Adenocarcinoma
title_full Germline Variants in DNA Damage Repair Genes: An Emerging Role in the Era of Precision Medicine in Pancreatic Adenocarcinoma
title_fullStr Germline Variants in DNA Damage Repair Genes: An Emerging Role in the Era of Precision Medicine in Pancreatic Adenocarcinoma
title_full_unstemmed Germline Variants in DNA Damage Repair Genes: An Emerging Role in the Era of Precision Medicine in Pancreatic Adenocarcinoma
title_short Germline Variants in DNA Damage Repair Genes: An Emerging Role in the Era of Precision Medicine in Pancreatic Adenocarcinoma
title_sort germline variants in dna damage repair genes an emerging role in the era of precision medicine in pancreatic adenocarcinoma
topic DDR genes
germline variants
pancreatic cancer
precision medicine
url https://doi.org/10.1002/ags3.12514
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AT andrewrbaker germlinevariantsindnadamagerepairgenesanemergingroleintheeraofprecisionmedicineinpancreaticadenocarcinoma
AT junyu germlinevariantsindnadamagerepairgenesanemergingroleintheeraofprecisionmedicineinpancreaticadenocarcinoma