Show simple item record

dc.contributor.authorBancroft, EK
dc.contributor.authorRaghallaigh, HN
dc.contributor.authorPage, EC
dc.contributor.authorEeles, RA
dc.date.accessioned2022-01-25T11:14:09Z
dc.date.available2022-01-25T11:14:09Z
dc.identifier.citationCurrent genetic medicine reports, 2021, 9 (4), pp. 47 - 58en_US
dc.identifier.issn2167-4876
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/4967
dc.identifier.eissn2167-4876en_US
dc.identifier.eissn2167-4876
dc.identifier.doi10.1007/s40142-021-00202-5en_US
dc.identifier.doi10.1007/s40142-021-00202-5
dc.description.abstract<h4>Purpose of review</h4>Prostate cancer (PrCa) is the most common cancer in men in the western world and is a major source of morbidity and mortality. Currently, general population PrCa screening is not recommended due to the limitations of the prostate-specific antigen (PSA) test. As such, there is increasing interest in identifying and screening higher-risk groups. The only established risk factors for PrCa are age, ethnicity, and having a family history of PrCa. A significant proportion of PrCa cases are caused by genetic factors.<h4>Recent findings</h4>Several rare germline variants have been identified that moderately increase risk of PrCa, and targeting screening to these men is proving useful at detecting clinically significant disease. The use of a "polygenic risk score" (PRS) that can calculate a man's personalized risk based on a number of lower-risk, but common genetic variants is the subject of ongoing research. Research efforts are currently focusing on the utility of screening in specific at-risk populations based on ethnicity, such as men of Black Afro-Caribbean descent. Whilst most screening studies have focused on use of PSA testing, the incorporation of additional molecular and genomic biomarkers alongside increasingly sophisticated imaging modalities is being designed to further refine and individualise both the screening and diagnostic pathway. Approximately 10% of men with advanced PrCa have a germline genetic predisposition leading to the opportunity for novel, targeted precision treatments.<h4>Summary</h4>The mainstreaming of genomics into the PrCa screening, diagnostic and treatment pathway will soon become standard practice and this review summarises current knowledge on genetic predisposition to PrCa and screening studies that are using genomics within their algorithms to target screening to higher-risk groups of men. Finally, we evaluate the importance of germline genetics beyond screening and diagnostics, and its role in the identification of lethal PrCa and in the selection of targeted treatments for advanced disease.en_US
dc.formatPrint-Electronicen_US
dc.format.extent47 - 58en_US
dc.languageengen_US
dc.language.isoengen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.titleUpdates in Prostate Cancer Research and Screening in Men at Genetically Higher Risk.en_US
dc.typeJournal Article
dcterms.dateAccepted2021-07-12
rioxxterms.versionVoRen_US
rioxxterms.versionofrecord10.1007/s40142-021-00202-5en_US
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0en_US
dc.relation.isPartOfCurrent genetic medicine reportsen_US
pubs.issue4en_US
pubs.notesNot knownen_US
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Oncogenetics
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Oncogenetics
pubs.publication-statusPublisheden_US
pubs.volume9en_US
pubs.embargo.termsNot knownen_US
icr.researchteamOncogenetics
dc.contributor.icrauthorEeles, Rosalinden_US


Files in this item

Thumbnail

This item appears in the following collection(s)

Show simple item record

http://creativecommons.org/licenses/by/4.0/
Except where otherwise noted, this item's license is described as http://creativecommons.org/licenses/by/4.0/