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DC Field | Value | Language |
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dc.contributor.author | Domchek S. | en |
dc.contributor.author | Blanco I. | en |
dc.contributor.author | Salinas M. | en |
dc.contributor.author | Cook J. | en |
dc.contributor.author | Rosario D.J. | en |
dc.contributor.author | Buys S. | en |
dc.contributor.author | Conner T. | en |
dc.contributor.author | Ausems M.G. | en |
dc.contributor.author | Ong K.-R. | en |
dc.contributor.author | Hoffman J. | en |
dc.contributor.author | Powers J. | en |
dc.contributor.author | Teixeira M.R. | en |
dc.contributor.author | Maia S. | en |
dc.contributor.author | Foulkes W.D. | en |
dc.contributor.author | Taherian N. | en |
dc.contributor.author | Ruijs M. | en |
dc.contributor.author | Den Enden A.T.H.-V. | en |
dc.contributor.author | Izatt L. | en |
dc.contributor.author | Davidson R. | en |
dc.contributor.author | Adank M.A. | en |
dc.contributor.author | Walker L. | en |
dc.contributor.author | Schmutzler R. | en |
dc.contributor.author | Tucker K. | en |
dc.contributor.author | Kirk J. | en |
dc.contributor.author | Hodgson S. | en |
dc.contributor.author | Harris M. | en |
dc.contributor.author | Douglas F. | en |
dc.contributor.author | Lindeman G.J. | en |
dc.contributor.author | Zgajnar J. | en |
dc.contributor.author | Tischkowitz M. | en |
dc.contributor.author | Clowes V.E. | en |
dc.contributor.author | Susman R. | en |
dc.contributor.author | Ramon Y Cajal T. | en |
dc.contributor.author | Patcher N. | en |
dc.contributor.author | Gadea N. | en |
dc.contributor.author | Spigelman A. | en |
dc.contributor.author | Van Os T. | en |
dc.contributor.author | Liljegren A. | en |
dc.contributor.author | Side L. | en |
dc.contributor.author | Brewer C. | en |
dc.contributor.author | Brady A.F. | en |
dc.contributor.author | Donaldson A. | en |
dc.contributor.author | Stefansdottir V. | en |
dc.contributor.author | Friedman E. | en |
dc.contributor.author | Chen-Shtoyerman R. | en |
dc.contributor.author | Amor D.J. | en |
dc.contributor.author | Copakova L. | en |
dc.contributor.author | Barwell J. | en |
dc.contributor.author | Giri V.N. | en |
dc.contributor.author | Murthy V. | en |
dc.contributor.author | Nicolai N. | en |
dc.contributor.author | Teo S.-H. | en |
dc.contributor.author | Greenhalgh L. | en |
dc.contributor.author | Strom S. | en |
dc.contributor.author | Henderson A. | en |
dc.contributor.author | McGrath J. | en |
dc.contributor.author | Gallagher D. | en |
dc.contributor.author | Aaronson N. | en |
dc.contributor.author | Ardern-Jones A. | en |
dc.contributor.author | Bangma C. | en |
dc.contributor.author | Dearnaley D. | en |
dc.contributor.author | Costello P. | en |
dc.contributor.author | Eyfjord J. | en |
dc.contributor.author | Rothwell J. | en |
dc.contributor.author | Falconer A. | en |
dc.contributor.author | Gronberg H. | en |
dc.contributor.author | Hamdy F.C. | en |
dc.contributor.author | Johannsson O. | en |
dc.contributor.author | Khoo V. | en |
dc.contributor.author | Kote-Jarai Z. | en |
dc.contributor.author | Lubinski J. | en |
dc.contributor.author | Axcrona U. | en |
dc.contributor.author | Melia J. | en |
dc.contributor.author | McKinley J. | en |
dc.contributor.author | Mitra A.V. | en |
dc.contributor.author | Moynihan C. | en |
dc.contributor.author | Rennert G. | en |
dc.contributor.author | Suri M. | en |
dc.contributor.author | Wilson P. | en |
dc.contributor.author | Killick E. | en |
dc.contributor.author | Moss S. | en |
dc.contributor.author | Eeles R.A. | en |
dc.contributor.author | Bancroft E.K. | en |
dc.contributor.author | Page E.C. | en |
dc.contributor.author | Castro E. | en |
dc.contributor.author | Lilja H. | en |
dc.contributor.author | Vickers A. | en |
dc.contributor.author | Sjoberg D. | en |
dc.contributor.author | Assel M. | en |
dc.contributor.author | Foster C.S. | en |
dc.contributor.author | Mitchell G. | en |
dc.contributor.author | Drew K. | en |
dc.contributor.author | Maehle L. | en |
dc.contributor.author | Axcrona K. | en |
dc.contributor.author | Evans D.G. | en |
dc.contributor.author | Bulman B. | en |
dc.contributor.author | Eccles D. | en |
dc.contributor.author | McBride D. | en |
dc.contributor.author | Van Asperen C. | en |
dc.contributor.author | Vasen H. | en |
dc.contributor.author | Kiemeney L.A. | en |
dc.contributor.author | Ringelberg J. | en |
dc.contributor.author | Cybulski C. | en |
dc.contributor.author | Wokolorczyk D. | en |
dc.contributor.author | Selkirk C. | en |
dc.contributor.author | Hulick P.J. | en |
dc.contributor.author | Bojesen A. | en |
dc.contributor.author | Skytte A.-B. | en |
dc.contributor.author | Lam J. | en |
dc.contributor.author | Taylor L. | en |
dc.contributor.author | Oldenburg R. | en |
dc.contributor.author | Cremers R. | en |
dc.contributor.author | Verhaegh G. | en |
dc.contributor.author | Van Zelst-Stams W.A. | en |
dc.contributor.author | Oosterwijk J.C. | en |
dc.date.accessioned | 2021-05-14T14:25:47Z | en |
dc.date.available | 2021-05-14T14:25:47Z | en |
dc.date.copyright | 2014 | en |
dc.date.created | 20140819 | en |
dc.date.issued | 2014-08-19 | - |
dc.date.issued | 2014-08-19 | en |
dc.identifier.citation | European Urology. 66 (3) (pp 489-499), 2014. Date of Publication: September 2014. | en |
dc.identifier.issn | 0302-2838 | en |
dc.identifier.uri | https://repository.monashhealth.org/monashhealthjspui/handle/1/42063 | en |
dc.description.abstract | Background Men with germline breast cancer 1, early onset (BRCA1) or breast cancer 2, early onset (BRCA2) gene mutations have a higher risk of developing prostate cancer (PCa) than noncarriers. IMPACT (Identification of Men with a genetic predisposition to ProstAte Cancer: Targeted screening in BRCA1/2 mutation carriers and controls) is an international consortium of 62 centres in 20 countries evaluating the use of targeted PCa screening in men with BRCA1/2 mutations. Objective To report the first year's screening results for all men at enrolment in the study. Design, setting and participants We recruited men aged 40-69 yr with germline BRCA1/2 mutations and a control group of men who have tested negative for a pathogenic BRCA1 or BRCA2 mutation known to be present in their families. All men underwent prostate-specific antigen (PSA) testing at enrolment, and those men with PSA >3 ng/ml were offered prostate biopsy. Outcome measurements and statistical analysis PSA levels, PCa incidence, and tumour characteristics were evaluated. The Fisher exact test was used to compare the number of PCa cases among groups and the differences among disease types. Results and limitations We recruited 2481 men (791 BRCA1 carriers, 531 BRCA1 controls; 731 BRCA2 carriers, 428 BRCA2 controls). A total of 199 men (8%) presented with PSA >3.0 ng/ml, 162 biopsies were performed, and 59 PCas were diagnosed (18 BRCA1 carriers, 10 BRCA1 controls; 24 BRCA2 carriers, 7 BRCA2 controls); 66% of the tumours were classified as intermediate- or high-risk disease. The positive predictive value (PPV) for biopsy using a PSA threshold of 3.0 ng/ml in BRCA2 mutation carriers was 48% - double the PPV reported in population screening studies. A significant difference in detecting intermediate- or high-risk disease was observed in BRCA2 carriers. Ninety-five percent of the men were white, thus the results cannot be generalised to all ethnic groups. Conclusions The IMPACT screening network will be useful for targeted PCa screening studies in men with germline genetic risk variants as they are discovered. These preliminary results support the use of targeted PSA screening based on BRCA genotype and show that this screening yields a high proportion of aggressive disease. Patient summary In this report, we demonstrate that germline genetic markers can be used to identify men at higher risk of prostate cancer. Targeting screening at these men resulted in the identification of tumours that were more likely to require treatment. © 2014 European Association of Urology. | en |
dc.language | English | en |
dc.language | en | en |
dc.title | Targeted prostate cancer screening in BRCA1 and BRCA2 mutation carriers: Results from the initial screening round of the IMPACT study. | en |
dc.type | Article | en |
dc.identifier.doi | http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1016/j.eururo.2014.01.003 | en |
dc.identifier.pubmedid | 24484606 [http://www.ncbi.nlm.nih.gov/pubmed/?term=24484606] | en |
dc.identifier.source | 52980392 | en |
dc.identifier.institution | (Bancroft, Ardern-Jones, Dearnaley, Khoo, Killick, Eeles) Cancer Genetics Unit and Academic Urology Unit, Royal Marsden NHS Foundation Trust, London, United Kingdom (Bancroft, Page, Castro, Dearnaley, Kote-Jarai, Mitra, Moynihan, Killick, Eeles) Oncogenetics Team, Institute of Cancer Research, London, United Kingdom (Castro) Spanish National Cancer Research Centre, Madrid, Spain (Lilja) Departments of Laboratory Medicine, Surgery and Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY, United States (Lilja, Hamdy) Nuffield Department of Surgical Sciences, University of Oxford, Oxford, United Kingdom (Lilja) Institute of Biomedical Technology, University of Tampere, Tampere, Finland (Lilja) Department of Laboratory Medicine, Lund University, Malmo, Sweden (Vickers, Sjoberg, Assel) Department of Epidemiology and Biostatistics, Memorial Sloan-Kettering Cancer Center, New York, NY, United States (Foster) HCA Healthcare Laboratories, London, WC1E 6JA, United Kingdom (Mitchell, Drew, McKinley) Familial Cancer Centre, Peter MacCallum Cancer Centre, East Melbourne, VIC, Australia (Mitchell) Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, VIC, Australia (Maehle, Axcrona, Axcrona) Norwegian Radium Hospital, Oslo, Norway (Evans, Bulman, Rothwell) Genetic Medicine, Manchester Academic Health Sciences Centre, Central Manchester University Hospitals NHS Foundation Trust, Manchester, United Kingdom (Eccles, McBride, Costello) Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, United Kingdom (Van Asperen) Leiden University Medical Center, Leiden, Netherlands (Vasen, Ringelberg) Foundation for the Detection of Hereditary Tumours, Leiden, Netherlands (Kiemeney, Cremers, Verhaegh, Van Zelst-Stams) Radboud University Medical Centre, Nijmegen, Netherlands (Cybulski, Wokolorczyk, Lubinski) International Hereditary Cancer Center, Pomeranian Medical University, Szczecin, Poland (Selkirk, Hulick) Center for Medical Genetics, NorthShore University HealthSystem, Evanston, IL, United States (Hulick) Priztker School of Medicine, University of Chicago, Chicago, IL, United States (Bojesen, Skytte) Vejle Hospital, Vejle, Denmark (Lam, Taylor) Department of Urology, Repatriation General Hospital, Daw-Park, SA, Australia (Oldenburg, Bangma) Erasmus Medical Center, Rotterdam, Netherlands (Oosterwijk) University of Groningen, University Medical Center Groningen, Groningen, Netherlands (Blanco, Salinas) Hereditary Cancer Program, Catalonian Institute of Oncology, L'Hospitalet, Barcelona, Spain (Cook) Sheffield Clinical Genetics Service, Sheffield Children's Hospital, Sheffield, United Kingdom (Rosario) Royal Hallamshire Hospital, Sheffield, United Kingdom (Buys, Conner) Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, United States (Ausems) Department of Medical Genetics, University Medical Centre Utrecht, Netherlands (Ong, Hoffman) Clinical Genetics Unit, Birmingham Women's Hospital, Birmingham, United Kingdom (Domchek, Powers) Basser Research Center, University of Pennsylvania, Philadelphia, PA, United States (Teixeira, Maia) Genetics Department and Research Center, Portuguese Oncology Institute, Porto, Portugal (Teixeira) Biomedical Sciences Institute (ICBAS), Porto University, Porto, Portugal (Foulkes, Taherian) McGill Program in Cancer Genetics, Departments of Oncology and Human Genetics, McGill University, Montreal, QC, Canada (Ruijs, Aaronson) Netherlands Cancer Institute, Amsterdam, Netherlands (Den Enden) Maastricht University Medical Center, Department of Clinical Genetics, Maastricht, Netherlands (Izatt) South East Thames Genetics Service, London, United Kingdom (Davidson) Duncan Guthrie Institute of Medical Genetics, Yorkhill NHS Trust, Glasgow, United Kingdom (Adank) VU University Medical Center, Amsterdam, Netherlands (Walker, Hamdy) Churchill Hospital, Headington, Oxford, United Kingdom (Schmutzler) Center of Familial Breast and Ovarian Cancer, University Hospital of Cologne, Cologne, Germany (Tucker) Hereditary Cancer Clinic, Prince of Wales Hospital, Randwick, NSW, Australia (Tucker) Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia (Kirk) Familial Cancer Service, Westmead Hospital, Sydney, NSW, Australia (Kirk) Sydney Medical School (University of Sydney), Westmead Millennium Institute, Sydney, NSW, Australia (Hodgson) St. George's Hospital, Tooting, London, United Kingdom (Harris) Familial Cancer Centre, Monash Health, Clayton, VIC, Australia (Douglas, Henderson) Northern Genetics Service, Newcastle Upon Tyne Hospitals, Newcastle-upon-Tyne, United Kingdom (Lindeman) Familial Cancer Centre, Royal Melbourne Hospital, Parkville, VIC, Australia (Lindeman) Stem Cells and Cancer Division, Walter and Eliza Hall Institute of Medical Research, Parkville, VIC, Australia (Lindeman) Department of Medicine, University of Melbourne, Parkville, VIC, Australia (Zgajnar) Institute of Oncology, Ljubljana, Slovenia (Tischkowitz, Clowes) Addenbrooke's Hospital, Cambridge, United Kingdom (Tischkowitz, Clowes, Melia) University of Cambridge, Cambridge, United Kingdom (Susman) Genetic Health Queensland, Royal Brisbane and Women's Hospital, Herston, QLD, Australia (Ramon Y Cajal) Hospital de Sant Pau, Barcelona, Spain (Patcher) Genetic Services of WA, King Edward Memorial Hospital, Subiaco, WA, Australia (Patcher) Department of Paediatrics, University of Western Australia, Perth, WA, Australia (Gadea) Hospital Vall d'Hebron, Barcelona, Spain (Spigelman) Hunter Family Cancer Service, Waratah, NSW, Australia (Spigelman) University of New South Wales, St. Vincent's Clinical School, Darlinghurst, NSW, Australia (Spigelman) Hereditary Cancer Clinic, Kinghorn Cancer Centre, St. Vincent's Hospital, Sydney, NSW, Australia (Van Os) Academic Medical Center, Amsterdam, Netherlands (Liljegren) Karolinska University Hospital, Karolinska Institute, Stockholm, Sweden (Side) NE Thames Regional Genetics Service, Institute of Child Health, London, United Kingdom (Brewer) Peninsular Genetics, Derriford Hospital, Plymouth, United Kingdom (Brewer, McGrath) Royal Devon and Exeter Hospital, Exeter, United Kingdom (Brady) North West Thames Regional Genetics Service, Kennedy-Galton Centre, North West London Hospitals NHS Trust, Harrow, United Kingdom (Donaldson) St. Michael's Hospital, Bristol, United Kingdom (Stefansdottir, Johannsson) Landspitali-the National University Hospital of Iceland, Reykjavik, Iceland (Friedman) Chaim Shema Medical Center, Tel-Hashomer, Israel (Chen-Shtoyerman) Genetic Institute, Kaplan Medical Center, Rehovot, Israel (Amor) Murdoch Childrens Research Institute, Parkville, VIC, United States (Copakova) National Cancer Institute, Bratislava, Slovakia (Barwell) University of Leicester, Leicester, United Kingdom (Barwell) University Hospitals Leicester, Leicester, United Kingdom (Giri) Fox Chase Cancer Center, Philadelphia, PA, United States (Murthy) Tata Memorial Centre, Mumbai, India (Nicolai) Istituto Nazionale dei Tumori, Milan, Italy (Teo) Cancer Research Initiatives Foundation, Subang Jaya Medical Centre, Selangor, Darul Ehsan, Malaysia (Greenhalgh) Clinical Genetics, Royal Liverpool Children's Hospital, Liverpool, United Kingdom (Strom) University of Texas, MD Anderson Cancer Center, Houston, TX, United States (Gallagher) Mater Misericordiae University Hospital, Dublin, Ireland (Eyfjord) Faculty of Medicine, School of Health Sciences, University of Iceland, Reykjavik, Iceland (Falconer) Imperial College Healthcare NHS Trust, London, London, United Kingdom (Gronberg) University Hospital, Umea, Sweden (Mitra) University College London Hospitals NHS Foundation Trust, London, United Kingdom (Rennert) CHS National Cancer Control Center, Carmel Medical Center, Haifa, Israel (Suri) Nottingham City Hospital, Nottingham, United Kingdom (Wilson) BioZenix, Altrincham, Cheshire, United Kingdom (Moss) Queen Mary University of London, London, United Kingdom | en |
dc.description.address | R.A. Eeles, Institute of Cancer Research, Royal Marsden NHS Foundation Trust, 15 Cotswold Road, Sutton SM2 5NG, United Kingdom. E-mail: rosalind.eeles@icr.ac.uk | en |
dc.description.publicationstatus | Embase | en |
dc.rights.statement | Copyright 2016 Elsevier B.V., All rights reserved. | en |
dc.subect.keywords | BRCA1 BRCA2 Prostate cancer Prostate-specific antigen Targeted screening | en |
dc.identifier.authoremail | Eeles R.A.; rosalind.eeles@icr.ac.uk | en |
dc.description.grant | No: P50-CA92629 Organization: (NCI) *National Cancer Institute* No: PCFA PR04 Organization: (PCFA) *Prostate Cancer Foundation of Australia* No: R01 CA175491 Organization: (NCI) *National Cancer Institute* No: R01CA160816 Organization: (NCI) *National Cancer Institute* | en |
item.fulltext | No Fulltext | - |
item.cerifentitytype | Publications | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.grantfulltext | none | - |
item.openairetype | Article | - |
crisitem.author.dept | Oncology | - |
Appears in Collections: | Articles |
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