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Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition.
Mikropoulos, Christos; Selkirk, Christina G Hutten; Saya, Sibel; Bancroft, Elizabeth; Vertosick, Emily; Dadaev, Tokhir; Brendler, Charles; Page, Elizabeth; Dias, Alexander; Evans, D Gareth; Rothwell, Jeanette; Maehle, Lovise; Axcrona, Karol; Richardson, Kate; Eccles, Diana; Jensen, Thomas; Osther, Palle J; van Asperen, Christi J; Vasen, Hans; Kiemeney, Lambertus A; Ringelberg, Janneke; Cybulski, Cezary; Wokolorczyk, Dominika; Hart, Rachel; Glover, Wayne; Lam, Jimmy; Taylor, Louise; Salinas, Monica; Feliubadaló, Lidia; Oldenburg, Rogier; Cremers, Ruben; Verhaegh, Gerald; van Zelst-Stams, Wendy A; Oosterwijk, Jan C; Cook, Jackie; Rosario, Derek J; Buys, Saundra S; Conner, Tom; Domchek, Susan; Powers, Jacquelyn; Ausems, Margreet Gem; Teixeira, Manuel R; Maia, Sofia; Izatt, Louise; Schmutzler, Rita; Rhiem, Kerstin; Foulkes, William D; Boshari, Talia; Davidson, Rosemarie; Ruijs, Marielle.
Afiliação
  • Mikropoulos C; The Institute of Cancer Research, 15 Cotswold Road, Sutton, Surrey SM2 5NG, UK.
  • Selkirk CGH; The John and Carol Walter Center for Urological Health, Department of Surgery, North Shore University Health System, Evanston, IL 60201, USA.
  • Saya S; Center for Medical Genetics, Department of Medicine, NorthShore University HealthSystem, Evanston, IL 60201, USA.
  • Bancroft E; The Institute of Cancer Research, 15 Cotswold Road, Sutton, Surrey SM2 5NG, UK.
  • Vertosick E; The Institute of Cancer Research, 15 Cotswold Road, Sutton, Surrey SM2 5NG, UK.
  • Dadaev T; Royal Marsden NHS Foundation Trust, Fulham Rd, London SW3 6JJ, UK.
  • Brendler C; Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
  • Page E; The Institute of Cancer Research, 15 Cotswold Road, Sutton, Surrey SM2 5NG, UK.
  • Dias A; The John and Carol Walter Center for Urological Health, Department of Surgery, North Shore University Health System, Evanston, IL 60201, USA.
  • Evans DG; The Institute of Cancer Research, 15 Cotswold Road, Sutton, Surrey SM2 5NG, UK.
  • Rothwell J; The Institute of Cancer Research, 15 Cotswold Road, Sutton, Surrey SM2 5NG, UK.
  • Maehle L; Royal Marsden NHS Foundation Trust, Fulham Rd, London SW3 6JJ, UK.
  • Axcrona K; Genomic Medicine, Manchester Academic Health Sciences Centre, Division of Evolution and Genomic Sciences, University of Manchester, Central Manchester University Hospitals NHS Foundation Trust, Manchester M13 9WL, UK.
  • Richardson K; Genomic Medicine, Manchester Academic Health Sciences Centre, Division of Evolution and Genomic Sciences, University of Manchester, Central Manchester University Hospitals NHS Foundation Trust, Manchester M13 9WL, UK.
  • Eccles D; Department of Medical Genetics, Oslo University Hospital, Oslo 0372, Norway.
  • Jensen T; Akershus University Hospital, Lørenskog 1478, Norway.
  • Osther PJ; Parkville Familial Cancer Centre, Peter MacCallum Cancer Centre, East Melbourne, VIC 3000, Australia.
  • van Asperen CJ; The Sir Peter MacCallum Department of Oncology, University of Melbourne, VIC 3010, Australia.
  • Vasen H; Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton SO16 5YA, UK.
  • Kiemeney LA; Cancer Sciences, Faculty of Medicine, University of Southampton, University Hospital Southampton NHS Foundation Trust, Southampton SO16 6YD, UK.
  • Ringelberg J; Department of Clinical Genetics, Vejle Hospital, Vejle 7100, Denmark.
  • Cybulski C; Department of Clinical Genetics, Vejle Hospital, Vejle 7100, Denmark.
  • Wokolorczyk D; Leiden University Medical Center, Department of Clinical Genetics, Leiden, ZA 2333, The Netherlands.
  • Hart R; Netherlands Foundation for the Detection of Hereditary Tumors, Leiden, ZA 2333, The Netherlands.
  • Glover W; Radboud University Medical Center, Nijmegen, GA 6525, The Netherlands.
  • Lam J; Netherlands Foundation for the Detection of Hereditary Tumors, Leiden, ZA 2333, The Netherlands.
  • Taylor L; International Hereditary Cancer Center, Department of Genetics and Pathology, Pomeranian Medical University, Szczecin 70-204, Poland.
  • Salinas M; International Hereditary Cancer Center, Department of Genetics and Pathology, Pomeranian Medical University, Szczecin 70-204, Poland.
  • Feliubadaló L; Clinical Genetics Unit, Birmingham Women's Hospital, Birmingham B15 2TG, UK.
  • Oldenburg R; Clinical Genetics Unit, Birmingham Women's Hospital, Birmingham B15 2TG, UK.
  • Cremers R; Department of Urology, Repatriation General Hospital, Daw Park, SA 5041, Australia.
  • Verhaegh G; Department of Urology, Repatriation General Hospital, Daw Park, SA 5041, Australia.
  • van Zelst-Stams WA; Hereditary Cancer Program, Catalan Institute of Oncology (ICO-IDIBELL, CIBERONC), L'Hospitalet de Llobregat, Barcelona 08908, Spain.
  • Oosterwijk JC; Hereditary Cancer Program, Catalan Institute of Oncology (ICO-IDIBELL, CIBERONC), L'Hospitalet de Llobregat, Barcelona 08908, Spain.
  • Cook J; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam 3015 CE, The Netherlands.
  • Rosario DJ; Radboud University Medical Center, Nijmegen, GA 6525, The Netherlands.
  • Buys SS; Radboud University Medical Center, Nijmegen, GA 6525, The Netherlands.
  • Conner T; Netherlands Foundation for the Detection of Hereditary Tumors, Leiden, ZA 2333, The Netherlands.
  • Domchek S; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen 9713 GZ, The Netherlands.
  • Powers J; Sheffield Clinical Genetics Service, Sheffield Children's Hospital, Sheffield S10 2TH, UK.
  • Ausems MG; Royal Hallamshire Hospital, Sheffield S10 2JF, UK.
  • Teixeira MR; Huntsman Cancer Institute at the University of Utah, Salt Lake City, UT 84103, USA.
  • Maia S; Huntsman Cancer Institute at the University of Utah, Salt Lake City, UT 84103, USA.
  • Izatt L; Basser Research Center, University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Schmutzler R; Basser Research Center, University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Rhiem K; Department of Genetics, University Medical Centre Utrecht, Utrecht, CX, The Netherlands.
  • Foulkes WD; Genetics Department and Research Center, Portuguese Oncology Institute, Porto 4200-072, Portugal.
  • Boshari T; Biomedical Sciences Institute (ICBAS), Porto University, Porto 4200-072, Portugal.
  • Davidson R; Genetics Department and Research Center, Portuguese Oncology Institute, Porto 4200-072, Portugal.
  • Ruijs M; South East Thames Genetics Service, Guy's Hospital, London SE1 9RT, UK.
Br J Cancer ; 118(2): 266-276, 2018 01.
Article em En | MEDLINE | ID: mdl-29301143
BACKGROUND: Prostate-specific antigen (PSA) and PSA-velocity (PSAV) have been used to identify men at risk of prostate cancer (PrCa). The IMPACT study is evaluating PSA screening in men with a known genetic predisposition to PrCa due to BRCA1/2 mutations. This analysis evaluates the utility of PSA and PSAV for identifying PrCa and high-grade disease in this cohort. METHODS: PSAV was calculated using logistic regression to determine if PSA or PSAV predicted the result of prostate biopsy (PB) in men with elevated PSA values. Cox regression was used to determine whether PSA or PSAV predicted PSA elevation in men with low PSAs. Interaction terms were included in the models to determine whether BRCA status influenced the predictiveness of PSA or PSAV. RESULTS: 1634 participants had ⩾3 PSA readings of whom 174 underwent PB and 45 PrCas diagnosed. In men with PSA >3.0 ng ml-l, PSAV was not significantly associated with presence of cancer or high-grade disease. PSAV did not add to PSA for predicting time to an elevated PSA. When comparing BRCA1/2 carriers to non-carriers, we found a significant interaction between BRCA status and last PSA before biopsy (P=0.031) and BRCA2 status and PSAV (P=0.024). However, PSAV was not predictive of biopsy outcome in BRCA2 carriers. CONCLUSIONS: PSA is more strongly predictive of PrCa in BRCA carriers than non-carriers. We did not find evidence that PSAV aids decision-making for BRCA carriers over absolute PSA value alone.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Calicreínas / Antígeno Prostático Específico Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Adult / Aged / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Calicreínas / Antígeno Prostático Específico Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Adult / Aged / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article