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dc.contributor.authorBenafif, S
dc.contributor.authorNi Raghallaigh, H
dc.contributor.authorMcGrowder, E
dc.contributor.authorSaunders, EJ
dc.contributor.authorBrook, MN
dc.contributor.authorSaya, S
dc.contributor.authorRageevakumar, R
dc.contributor.authorWakerell, S
dc.contributor.authorJames, D
dc.contributor.authorChamberlain, A
dc.contributor.authorTaylor, N
dc.contributor.authorHogben, M
dc.contributor.authorBenton, B
dc.contributor.authorD'Mello, L
dc.contributor.authorMyhill, K
dc.contributor.authorMikropoulos, C
dc.contributor.authorBowen-Perkins, H
dc.contributor.authorRafi, I
dc.contributor.authorFerris, M
dc.contributor.authorBeattie, A
dc.contributor.authorKuganolipava, S
dc.contributor.authorSevenoaks, T
dc.contributor.authorBower, J
dc.contributor.authorKumar, P
dc.contributor.authorHazell, S
dc.contributor.authordeSouza, NM
dc.contributor.authorAntoniou, A
dc.contributor.authorBancroft, E
dc.contributor.authorKote-Jarai, Z
dc.contributor.authorEeles, R
dc.date.accessioned2021-08-20T14:27:05Z
dc.date.available2021-08-20T14:27:05Z
dc.date.issued2021-07-02
dc.identifier.citationBJU international, 2021
dc.identifier.issn1464-4096
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/4769
dc.identifier.eissn1464-410X
dc.identifier.doi10.1111/bju.15535
dc.description.abstractOBJECTIVES: To assess the feasibility and uptake of a community-based prostate cancer (PCa) screening programme selecting men according to their genetic risk of PCa. To assess the uptake of PCa screening investigations by men invited for screening. The uptake of the pilot study would guide the opening of the larger BARCODE1 study recruiting 5000 men. SUBJECTS AND METHODS: Healthy males aged 55-69 years were invited to participate via their general practitioners (GPs). Saliva samples were collected via mailed collection kits. After DNA extraction, genotyping was conducted using a study specific assay. Genetic risk was based on genotyping 130 germline PCa risk single nucleotide polymorphisms (SNPs). A polygenic risk score (PRS) was calculated for each participant using the sum of weighted alleles for 130 SNPs. Study participants with a PRS lying above the 90th centile value were invited for PCa screening by prostate magnetic resonance imaging (MRI) and biopsy. RESULTS: Invitation letters were sent to 1434 men. The overall study uptake was 26% (375/1436) and 87% of responders were eligible for study entry. DNA genotyping data were available for 297 men and 25 were invited for screening. After exclusions due to medical comorbidity/invitations declined, 18 of 25 men (72%) underwent MRI and biopsy of the prostate. There were seven diagnoses of PCa (38.9%). All cancers were low-risk and were managed with active surveillance. CONCLUSION: The BARCODE1 Pilot has shown this community study in the UK to be feasible, with an overall uptake of 26%. The main BARCODE1 study is now open and will recruit 5000 men. The results of BARCODE1 will be important in defining the role of genetic profiling in targeted PCa population screening. Patient Summary What is the paper about? Very few prostate cancer screening programmes currently exist anywhere in the world. Our pilot study investigated if men in the UK would find it acceptable to have a genetic test based on a saliva sample to examine their risk of prostate cancer development. This test would guide whether men are offered prostate cancer screening tests. What does it mean for patients? We found that the study design was acceptable: 26% of men invited to take part agreed to have the test. The majority of men who were found to have an increased genetic risk of prostate cancer underwent further tests offered (prostate MRI scan and biopsy). We have now expanded the study to enrol 5000 men. The BARCODE1 study will be important in examining whether this approach could be used for large-scale population prostate cancer screening.
dc.formatPrint-Electronic
dc.languageeng
dc.language.isoeng
dc.publisherWILEY
dc.rights.urihttps://creativecommons.org/licenses/by-nc-sa/4.0
dc.titleThe BARCODE1 Pilot: a feasibility study of using germline single nucleotide polymorphisms to target prostate cancer screening.
dc.typeJournal Article
dcterms.dateAccepted2021-06-23
rioxxterms.versionAM
rioxxterms.versionofrecord10.1111/bju.15535
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by-nc-sa/4.0
rioxxterms.licenseref.startdate2021-07-02
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfBJU international
pubs.notesNot known
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/Magnetic Resonance
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Oncogenetics
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.organisational-group/ICR/Students
pubs.organisational-group/ICR/Students/PhD and MPhil
pubs.organisational-group/ICR/Students/PhD and MPhil/18/19 Starting Cohort
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/Magnetic Resonance
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Oncogenetics
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.organisational-group/ICR/Students
pubs.organisational-group/ICR/Students/PhD and MPhil
pubs.organisational-group/ICR/Students/PhD and MPhil/18/19 Starting Cohort
pubs.publication-statusPublished
pubs.embargo.termsNot known
icr.researchteamMagnetic Resonance
icr.researchteamOncogenetics
icr.researchteamMagnetic Resonance
icr.researchteamOncogenetics
dc.contributor.icrauthorSaunders, Edward
dc.contributor.icrauthorBrook, Mark
dc.contributor.icrauthordeSouza, Nandita
dc.contributor.icrauthorKote-Jarai, Zsofia
dc.contributor.icrauthorEeles, Rosalind


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