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The IMPACT study is a multi\u2010national study of targeted prostate cancer (PrCa) screening in individuals with a known germline pathogenic variant (GPV) in either the BReast CAncer gene 1 (\n                      <jats:italic>BRCA1<\/jats:italic>\n                      ) or the BReast CAncer gene 2 (\n                      <jats:italic>BRCA2<\/jats:italic>\n                      ).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Subjects and Methods<\/jats:title>\n                    <jats:p>\n                      Participants enrolled in the\n                      <jats:styled-content style=\"fixed-case\">IMPACT<\/jats:styled-content>\n                      study were invited to complete a psychosocial questionnaire prior to each annual screening visit for a minimum of 5\u2009years. The questionnaire included questions on sociodemographics and the following measures: Hospital Anxiety and Depression Scale, Impact of Event Scale, 36\u2010item Short\u2010Form Health Survey, Memorial Anxiety Scale for\n                      <jats:styled-content style=\"fixed-case\">PrCa<\/jats:styled-content>\n                      , Cancer Worry Scale, risk perception and knowledge.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      A total of 760 participants completed questionnaires: 207 participants with\n                      <jats:styled-content style=\"fixed-case\">GPV<\/jats:styled-content>\n                      in\n                      <jats:styled-content style=\"fixed-case\">\n                        <jats:italic>BRCA1<\/jats:italic>\n                      <\/jats:styled-content>\n                      , 265 with\n                      <jats:styled-content style=\"fixed-case\">GPV<\/jats:styled-content>\n                      in\n                      <jats:styled-content style=\"fixed-case\">\n                        <jats:italic>BRCA2<\/jats:italic>\n                      <\/jats:styled-content>\n                      and 288 controls (non\u2010carriers from families with a known\n                      <jats:styled-content style=\"fixed-case\">GPV<\/jats:styled-content>\n                      ). We found no evidence of clinically concerning levels of general or cancer\u2010specific distress or poor health\u2010related quality of life in the cohort as a whole. Individuals in the control group had significantly less worry about\n                      <jats:styled-content style=\"fixed-case\">PrCa<\/jats:styled-content>\n                      compared with the carriers; however, all mean scores were low and within reported general population norms, where available.\n                      <jats:styled-content style=\"fixed-case\">\n                        <jats:italic>BRCA2<\/jats:italic>\n                      <\/jats:styled-content>\n                      carriers with previously high prostate\u2010specific antigen\n                      <jats:styled-content style=\"fixed-case\">(PSA)<\/jats:styled-content>\n                      levels experience a small but significant increase in\n                      <jats:styled-content style=\"fixed-case\">PrCa<\/jats:styled-content>\n                      anxiety (\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u20090.01) and\n                      <jats:styled-content style=\"fixed-case\">PSA<\/jats:styled-content>\n                      \u2010specific anxiety (\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&lt;\u20090.001). Cancer risk perceptions reflected information provided during genetic counselling and participants had good levels of knowledge, although this declined over time.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>\n                      This is the first study to report the longitudinal psychosocial impact of a targeted\n                      <jats:styled-content style=\"fixed-case\">PrCa<\/jats:styled-content>\n                      screening programme for\n                      <jats:styled-content style=\"fixed-case\">\n                        <jats:italic>BRCA1<\/jats:italic>\n                      <\/jats:styled-content>\n                      and\n                      <jats:styled-content style=\"fixed-case\">\n                        <jats:italic>BRCA2<\/jats:italic>\n                      <\/jats:styled-content>\n                      carriers. The results reassure that an annual\n                      <jats:styled-content style=\"fixed-case\">PSA<\/jats:styled-content>\n                      \u2010based screening programme does not have an adverse impact on psychosocial health or health\u2010related quality of life in these higher\u2010risk individuals. These results are important as more\n                      <jats:styled-content style=\"fixed-case\">PrCa<\/jats:styled-content>\n                      screening is targeted to higher\u2010risk groups.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/bju.16432","type":"journal-article","created":{"date-parts":[[2024,6,5]],"date-time":"2024-06-05T22:26:02Z","timestamp":1717626362000},"page":"484-500","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":8,"title":["The psychosocial impact of prostate cancer screening for\n                    <i>BRCA1<\/i>\n                    and\n                    <i>BRCA2<\/i>\n                    carriers"],"prefix":"10.1111","volume":"134","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-5482-5660","authenticated-orcid":false,"given":"Elizabeth K.","family":"Bancroft","sequence":"first","affiliation":[{"name":"Oncogenetics Team Royal Marsden NHS Foundation 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