TY - JOUR
T1 - The psychosocial impact of prostate cancer screening for BRCA1 and BRCA2 carriers
AU - IMPACT Study Steering Committee; IMPACT Collaborators
AU - Bancroft, Elizabeth K.
AU - Page, Elizabeth C.
AU - Brook, Mark N.
AU - Pope, Jennifer
AU - Thomas, Sarah
AU - Myhill, Kathryn
AU - Helfand, Brian T.
AU - Talaty, Pooja
AU - Ong, Kai Ren
AU - Douglas, Emma
AU - Cook, Jackie
AU - Rosario, Derek J.
AU - Salinas, Monica
AU - Buys, Saundra S.
AU - Anson, Jo
AU - Davidson, Rosemarie
AU - Longmuir, Mark
AU - Side, Lucy
AU - Eccles, Diana M.
AU - Tischkowitz, Marc
AU - Taylor, Amy
AU - Cruellas, Mara
AU - Ballestero, Eduard Perez
AU - Cleaver, Ruth
AU - Varughese, Mohini
AU - Barwell, Julian
AU - LeButt, Mandy
AU - Greenhalgh, Lynn
AU - Hart, Rachel
AU - Azzabi, Ashraf
AU - Jobson, Irene
AU - Cogley, Lynn
AU - Evans, D. Gareth
AU - Rothwell, Jeanette
AU - Taylor, Natalie
AU - Hogben, Matthew
AU - Saya, Sibel
AU - Kote-Jarai, Zsofia
AU - Ardern-Jones, Audrey
AU - Bangma, Chris
AU - Castro, Elena
AU - Dearnaley, David
AU - Eyfjord, Jorunn
AU - Falconer, Alison
AU - Foster, Christopher
AU - Grönberg, Henrik
AU - Hamdy, Freddie C.
AU - Jóhannsson, Óskar Þór
AU - Khoo, Vincent
AU - Chen-Shtoyerman, Rakefet
N1 - Publisher Copyright:
© 2024 The Author(s). BJU International published by John Wiley & Sons Ltd on behalf of BJU International.
PY - 2024/9
Y1 - 2024/9
N2 - 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.
AB - 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.
KW - BRCA1
KW - BRCA2
KW - genetic screening
KW - prostate cancer
KW - psychosocial
KW - quality of life
UR - https://www.scopus.com/pages/publications/85199880453
U2 - 10.1111/bju.16432
DO - 10.1111/bju.16432
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AN - SCOPUS:85199880453
SN - 1464-4096
VL - 134
SP - 484
EP - 500
JO - BJU International
JF - BJU International
IS - 3
ER -