Review on the Role of BRCA Mutations in Genomic Screening and Risk Stratification of Prostate Cancer

(1) Background: Somatic and germline alterations can be commonly found in prostate cancer (PCa) patients. The aim of our present study was to perform a comprehensive review of the current literature in order to examine the impact of BRCA mutations in the context of PCa as well as their significance...

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Main Authors: Nikolaos Kalampokis, Christos Zabaftis, Theodoros Spinos, Markos Karavitakis, Ioannis Leotsakos, Ioannis Katafigiotis, Henk van der Poel, Nikolaos Grivas, Dionysios Mitropoulos
Format: Article
Language:English
Published: MDPI AG 2024-02-01
Series:Current Oncology
Subjects:
Online Access:https://www.mdpi.com/1718-7729/31/3/86
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author Nikolaos Kalampokis
Christos Zabaftis
Theodoros Spinos
Markos Karavitakis
Ioannis Leotsakos
Ioannis Katafigiotis
Henk van der Poel
Nikolaos Grivas
Dionysios Mitropoulos
author_facet Nikolaos Kalampokis
Christos Zabaftis
Theodoros Spinos
Markos Karavitakis
Ioannis Leotsakos
Ioannis Katafigiotis
Henk van der Poel
Nikolaos Grivas
Dionysios Mitropoulos
author_sort Nikolaos Kalampokis
collection DOAJ
description (1) Background: Somatic and germline alterations can be commonly found in prostate cancer (PCa) patients. The aim of our present study was to perform a comprehensive review of the current literature in order to examine the impact of BRCA mutations in the context of PCa as well as their significance as genetic biomarkers. (2) Methods: A narrative review of all the available literature was performed. Only “landmark” publications were included. (3) Results: Overall, the number of PCa patients who harbor a BRCA2 mutation range between 1.2% and 3.2%. However, BRCA2 and BRCA1 mutations are responsible for most cases of hereditary PCa, increasing the risk by 3–8.6 times and up to 4 times, respectively. These mutations are correlated with aggressive disease and poor prognosis. Gene testing should be offered to patients with metastatic PCa, those with 2–3 first-degree relatives with PCa, or those aged < 55 and with one close relative with breast (age ≤ 50 years) or invasive ovarian cancer. (4) Conclusions: The individualized assessment of BRCA mutations is an important tool for the risk stratification of PCa patients. It is also a population screening tool which can guide our risk assessment strategies and achieve better results for our patients and their families.
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spelling doaj.art-6f7cc4fd9ae7442ea94424888ba810a12024-03-27T13:32:40ZengMDPI AGCurrent Oncology1198-00521718-77292024-02-013131162116910.3390/curroncol31030086Review on the Role of BRCA Mutations in Genomic Screening and Risk Stratification of Prostate CancerNikolaos Kalampokis0Christos Zabaftis1Theodoros Spinos2Markos Karavitakis3Ioannis Leotsakos4Ioannis Katafigiotis5Henk van der Poel6Nikolaos Grivas7Dionysios Mitropoulos8Department of Urology, G. Hatzikosta General Hospital, 45001 Ioannina, GreeceDepartment of Laparoscopy and Endourology, Central Urology, Lefkos Stavros the Athens Clinic, PC 11528 Athens, GreeceDepartment of Urology, University of Patras Hospital, 26504 Patras, GreeceDepartment of Laparoscopy and Endourology, Central Urology, Lefkos Stavros the Athens Clinic, PC 11528 Athens, GreeceDepartment of Laparoscopy and Endourology, Central Urology, Lefkos Stavros the Athens Clinic, PC 11528 Athens, GreeceDepartment of Laparoscopy and Endourology, Central Urology, Lefkos Stavros the Athens Clinic, PC 11528 Athens, GreeceDepartment of Urology, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, 1066 CX Amsterdam, The NetherlandsDepartment of Laparoscopy and Endourology, Central Urology, Lefkos Stavros the Athens Clinic, PC 11528 Athens, GreeceDepartment of Urology, Medical School, National & Kapodistrian University of Athens, 14122 Athens, Greece(1) Background: Somatic and germline alterations can be commonly found in prostate cancer (PCa) patients. The aim of our present study was to perform a comprehensive review of the current literature in order to examine the impact of BRCA mutations in the context of PCa as well as their significance as genetic biomarkers. (2) Methods: A narrative review of all the available literature was performed. Only “landmark” publications were included. (3) Results: Overall, the number of PCa patients who harbor a BRCA2 mutation range between 1.2% and 3.2%. However, BRCA2 and BRCA1 mutations are responsible for most cases of hereditary PCa, increasing the risk by 3–8.6 times and up to 4 times, respectively. These mutations are correlated with aggressive disease and poor prognosis. Gene testing should be offered to patients with metastatic PCa, those with 2–3 first-degree relatives with PCa, or those aged < 55 and with one close relative with breast (age ≤ 50 years) or invasive ovarian cancer. (4) Conclusions: The individualized assessment of BRCA mutations is an important tool for the risk stratification of PCa patients. It is also a population screening tool which can guide our risk assessment strategies and achieve better results for our patients and their families.https://www.mdpi.com/1718-7729/31/3/86prostate cancergenomic screeningmutations
spellingShingle Nikolaos Kalampokis
Christos Zabaftis
Theodoros Spinos
Markos Karavitakis
Ioannis Leotsakos
Ioannis Katafigiotis
Henk van der Poel
Nikolaos Grivas
Dionysios Mitropoulos
Review on the Role of BRCA Mutations in Genomic Screening and Risk Stratification of Prostate Cancer
Current Oncology
prostate cancer
genomic screening
mutations
title Review on the Role of BRCA Mutations in Genomic Screening and Risk Stratification of Prostate Cancer
title_full Review on the Role of BRCA Mutations in Genomic Screening and Risk Stratification of Prostate Cancer
title_fullStr Review on the Role of BRCA Mutations in Genomic Screening and Risk Stratification of Prostate Cancer
title_full_unstemmed Review on the Role of BRCA Mutations in Genomic Screening and Risk Stratification of Prostate Cancer
title_short Review on the Role of BRCA Mutations in Genomic Screening and Risk Stratification of Prostate Cancer
title_sort review on the role of brca mutations in genomic screening and risk stratification of prostate cancer
topic prostate cancer
genomic screening
mutations
url https://www.mdpi.com/1718-7729/31/3/86
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