دورية أكاديمية

Prevention, diagnosis and clinical management of hereditary breast cancer beyond BRCA1/2 genes.

التفاصيل البيبلوغرافية
العنوان: Prevention, diagnosis and clinical management of hereditary breast cancer beyond BRCA1/2 genes.
المؤلفون: Calabrese, A, von Arx, C, Tafuti, A A, Pensabene, M, De Laurentiis, M
المصدر: Cancer Treat Rev ; ISSN:1532-1967 ; Volume:129
بيانات النشر: Elsevier Science
سنة النشر: 2024
المجموعة: PubMed Central (PMC)
مصطلحات موضوعية: BRCA genes, Hereditary breast cancer, Multi-gene panel testing, NGS, VUS
الوصف: The detection of germline pathogenic variants (gPVs) in BRCA1/2 and other breast cancer (BC) genes is rising exponentially thanks to the advent of multi-gene panel testing. This promising technology, coupled with the availability of specific therapies for BC BRCA-related, has increased the number of patients eligible for genetic testing. Implementing multi-gene panel testing for hereditary BC screening holds promise to maximise benefits for patients at hereditary risk of BC. These benefits range from prevention programs to antineoplastic-targeted therapies. However, the clinical management of these patients is complex and requires guidelines based on recent evidence. Furthermore, applying multi-gene panel testing into clinical practice increases the detection of variants of uncertain significance (VUSs). This augments the complexity of patients' clinical management, becoming an unmet need for medical oncologists. This review aims to collect updated evidence on the most common BC-related genes besides BRCA1/2, from their biological role in BC development to their potential impact in tailoring prevention and treatment strategies.
نوع الوثيقة: article in journal/newspaper
review
اللغة: English
العلاقة: https://doi.org/10.1016/j.ctrv.2024.102785Test; https://pubmed.ncbi.nlm.nih.gov/38870570Test
DOI: 10.1016/j.ctrv.2024.102785
الإتاحة: https://doi.org/10.1016/j.ctrv.2024.102785Test
https://pubmed.ncbi.nlm.nih.gov/38870570Test
حقوق: Copyright © 2024. Published by Elsevier Ltd.
رقم الانضمام: edsbas.EB882ED1
قاعدة البيانات: BASE