Prostate cancer and homologous recombination repair gene mutations: a monocentric observational study on clinical and histopathological features and their association with oncological outcomes

Fuente: Zenodo
Salvato in:
Dettagli Bibliografici
Autori principali: Rossetti, Sabrina, Coppola, Elisabetta
Natura: Recurso digital
Pubblicazione: Zenodo 2025
Accesso online:
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne!!
_version_ 1866901132333285376
author Rossetti, Sabrina
Coppola, Elisabetta
author_facet Rossetti, Sabrina
Coppola, Elisabetta
contents <p><span lang="EN-US">This study provides real-world evidence that homologous recombination repair (HRR) gene mutations, particularly in <em>BRCA2</em>, are associated with more aggressive clinical and pathological features in patients with metastatic hormone-sensitive prostate cancer (mHSPC). Importantly, mutations located in functional domains of <em>BRCA2</em>, such as the DNA-binding domain and exon 11, were linked to worse oncological outcomes. The findings suggest that not all <em>BRCA2</em> mutations carry the same prognostic value. These results support the potential utility of detailed genetic profiling for risk stratification and treatment personalization in mHSPC.</span></p>
format Recurso digital
id zenodo_https___doi_org_10_5281_zenodo_15189983
institution Zenodo
language
publishDate 2025
publisher Zenodo
record_format zenodo
spellingShingle Prostate cancer and homologous recombination repair gene mutations: a monocentric observational study on clinical and histopathological features and their association with oncological outcomes
Rossetti, Sabrina
Coppola, Elisabetta
<p><span lang="EN-US">This study provides real-world evidence that homologous recombination repair (HRR) gene mutations, particularly in <em>BRCA2</em>, are associated with more aggressive clinical and pathological features in patients with metastatic hormone-sensitive prostate cancer (mHSPC). Importantly, mutations located in functional domains of <em>BRCA2</em>, such as the DNA-binding domain and exon 11, were linked to worse oncological outcomes. The findings suggest that not all <em>BRCA2</em> mutations carry the same prognostic value. These results support the potential utility of detailed genetic profiling for risk stratification and treatment personalization in mHSPC.</span></p>
title Prostate cancer and homologous recombination repair gene mutations: a monocentric observational study on clinical and histopathological features and their association with oncological outcomes
url https://doi.org/10.5281/zenodo.15189983