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The psychosocial impact of prostate cancer screening for BRCA1 and BRCA2 carriers.
Bancroft, Elizabeth K; Page, Elizabeth C; Brook, Mark N; Pope, Jennifer; Thomas, Sarah; Myhill, Kathryn; Helfand, Brian T; Talaty, Pooja; Ong, Kai-Ren; Douglas, Emma; Cook, Jackie; Rosario, Derek J; Salinas, Monica; Buys, Saundra S; Anson, Jo; Davidson, Rosemarie; Longmuir, Mark; Side, Lucy; Eccles, Diana M; Tischkowitz, Marc; Taylor, Amy; Cruellas, Mara; Ballestero, Eduard Perez; Cleaver, Ruth; Varughese, Mohini; Barwell, Julian; LeButt, Mandy; Greenhalgh, Lynn; Hart, Rachel; Azzabi, Ashraf; Jobson, Irene; Cogley, Lynn; Evans, D Gareth; Rothwell, Jeanette; Taylor, Natalie; Hogben, Matthew; Saya, Sibel; Eeles, Rosalind A; Aaronson, Neil K.
Afiliação
  • Bancroft EK; Oncogenetics Team, Royal Marsden NHS Foundation Trust, London, UK.
  • Page EC; Oncogenetics Team, Institute of Cancer Research, London, UK.
  • Brook MN; Oncogenetics Team, Institute of Cancer Research, London, UK.
  • Pope J; Oncogenetics Team, Institute of Cancer Research, London, UK.
  • Thomas S; Oncogenetics Team, Institute of Cancer Research, London, UK.
  • Myhill K; Oncogenetics Team, Royal Marsden NHS Foundation Trust, London, UK.
  • Helfand BT; Oncogenetics Team, Royal Marsden NHS Foundation Trust, London, UK.
  • Talaty P; Division of Urology, John and Carol Walter Center for Urological Health, NorthShore University HealthSystem, Evanston, IL, USA.
  • Ong KR; Division of Urology, John and Carol Walter Center for Urological Health, NorthShore University HealthSystem, Evanston, IL, USA.
  • Douglas E; West Midlands Regional Clinical Genetics Service, Birmingham Women's Hospital, Birmingham, UK.
  • Cook J; West Midlands Regional Clinical Genetics Service, Birmingham Women's Hospital, Birmingham, UK.
  • Rosario DJ; Sheffield Clinical Genetics Service, Sheffield Children's Hospital, Sheffield, UK.
  • Salinas M; Royal Hallamshire Hospital, Sheffield, UK.
  • Buys SS; Hereditary Cancer Program, ICO (Catalan Institute of Oncology), Barcelona, Spain.
  • Anson J; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
  • Davidson R; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
  • Longmuir M; West of Scotland Genetic Service, Queen Elizabeth University Hospital, Glasgow, UK.
  • Side L; West of Scotland Genetic Service, Queen Elizabeth University Hospital, Glasgow, UK.
  • Eccles DM; Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, UK.
  • Tischkowitz M; Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, UK.
  • Taylor A; The University of Southampton Medical School, Southampton, UK.
  • Cruellas M; East Anglian Medical Genetics Service, Cambridge University Hospitals NHS Trust, Cambridge, UK.
  • Ballestero EP; Department of Medical Genetics, NIHR Cambridge Biomedical Research Centre, University of Cambridge, Cambridge, UK.
  • Cleaver R; East Anglian Medical Genetics Service, Cambridge University Hospitals NHS Trust, Cambridge, UK.
  • Varughese M; Hereditary Cancer Genetics Group, Medical Oncology Department, Hospital Vall d'Hebron, Vall d'Hebron Institute of Oncology, Barcelona, Spain.
  • Barwell J; Hereditary Cancer Genetics Group, Medical Oncology Department, Hospital Vall d'Hebron, Vall d'Hebron Institute of Oncology, Barcelona, Spain.
  • LeButt M; Peninsula Clinical Genetics Service, Royal Devon University Healthcare NHS Foundation Trust, Exeter, UK.
  • Greenhalgh L; Peninsula Clinical Genetics Service, Royal Devon University Healthcare NHS Foundation Trust, Exeter, UK.
  • Hart R; University of Leicester, Leicester, UK.
  • Azzabi A; University Hospitals Leicester, Leicester, UK.
  • Jobson I; University Hospitals Leicester, Leicester, UK.
  • Cogley L; Liverpool Centre for Genomic Medicine, Liverpool Women's NHS Foundation Trust, Liverpool, UK.
  • Evans DG; Liverpool Centre for Genomic Medicine, Liverpool Women's NHS Foundation Trust, Liverpool, UK.
  • Rothwell J; Northern Centre for Cancer Care, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle, UK.
  • Taylor N; Northern Centre for Cancer Care, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle, UK.
  • Hogben M; Peninsular Genetics, Derriford Hospital, Plymouth, UK.
  • Saya S; Genomic Medicine, Manchester Academic Health Sciences Centre, Manchester University NHS Foundation Trust, Manchester, UK.
  • Eeles RA; Oncogenetics Team, Royal Marsden NHS Foundation Trust, London, UK.
  • Aaronson NK; Oncogenetics Team, Royal Marsden NHS Foundation Trust, London, UK.
BJU Int ; 2024 Jun 05.
Article em En | MEDLINE | ID: mdl-38839570
ABSTRACT

OBJECTIVES:

To report the long-term outcomes from a longitudinal psychosocial study that forms part of the 'Identification of Men with a genetic predisposition to ProstAte Cancer Targeted Screening in men at higher genetic risk and controls' (IMPACT) study. The IMPACT study is a multi-national study of targeted prostate cancer (PrCa) screening in individuals with a known germline pathogenic variant (GPV) in either the BReast CAncer gene 1 (BRCA1) or the BReast CAncer gene 2 (BRCA2). SUBJECTS AND

METHODS:

Participants enrolled in the IMPACT study were invited to complete a psychosocial questionnaire prior to each annual screening visit for a minimum of 5 years. The questionnaire included questions on sociodemographics and the following

measures:

Hospital Anxiety and Depression Scale, Impact of Event Scale, 36-item Short-Form Health Survey, Memorial Anxiety Scale for PrCa, Cancer Worry Scale, risk perception and knowledge.

RESULTS:

A total of 760 participants completed questionnaires 207 participants with GPV in BRCA1, 265 with GPV in BRCA2 and 288 controls (non-carriers from families with a known GPV). We found no evidence of clinically concerning levels of general or cancer-specific distress or poor health-related quality of life in the cohort as a whole. Individuals in the control group had significantly less worry about PrCa compared with the carriers; however, all mean scores were low and within reported general population norms, where available. BRCA2 carriers with previously high prostate-specific antigen (PSA) levels experience a small but significant increase in PrCa anxiety (P = 0.01) and PSA-specific anxiety (P < 0.001). Cancer risk perceptions reflected information provided during genetic counselling and participants had good levels of knowledge, although this declined over time.

CONCLUSION:

This is the first study to report the longitudinal psychosocial impact of a targeted PrCa screening programme for BRCA1 and BRCA2 carriers. The results reassure that an annual PSA-based screening programme does not have an adverse impact on psychosocial health or health-related quality of life in these higher-risk individuals. These results are important as more PrCa screening is targeted to higher-risk groups.
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Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: BJU Int Assunto da revista: UROLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: BJU Int Assunto da revista: UROLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido