{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,2]],"date-time":"2026-08-02T23:23:21Z","timestamp":1785713001902,"version":"3.56.0"},"reference-count":30,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2015,5,24]],"date-time":"2015-05-24T00:00:00Z","timestamp":1432425600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"name":"Beckman Coulter UK Ltd."}],"content-domain":{"domain":["bjui-journals.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["BJU International"],"published-print":{"date-parts":[[2016,3]]},"abstract":"<jats:sec>\n                    <jats:title>Objectives<\/jats:title>\n                    <jats:p>\n                      To analyse the clinical utility of a prediction model\u00a0incorporating both clinical information and a novel\u00a0biomarker, p2\n                      <jats:styled-content style=\"fixed-case\">PSA<\/jats:styled-content>\n                      , in order to inform the decision\u00a0for prostate biopsy in an Irish cohort of men referred for prostate cancer assessment.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Patients and Methods<\/jats:title>\n                    <jats:p>\n                      Serum isolated from 250 men from three tertiary referral\u00a0centres with pre\u2010biopsy blood draws was analysed for total prostate\u2010specific antigen (\n                      <jats:styled-content style=\"fixed-case\">PSA<\/jats:styled-content>\n                      ), free\n                      <jats:styled-content style=\"fixed-case\">PSA<\/jats:styled-content>\n                      (\n                      <jats:styled-content style=\"fixed-case\">fPSA<\/jats:styled-content>\n                      )\u00a0and p2\n                      <jats:styled-content style=\"fixed-case\">PSA<\/jats:styled-content>\n                      . From this, the Prostate Health Index (\n                      <jats:styled-content style=\"fixed-case\">PHI<\/jats:styled-content>\n                      ) score was calculated (\n                      <jats:styled-content style=\"fixed-case\">PHI<\/jats:styled-content>\n                      = (p2\n                      <jats:styled-content style=\"fixed-case\">PSA<\/jats:styled-content>\n                      \/\n                      <jats:styled-content style=\"fixed-case\">fPSA<\/jats:styled-content>\n                      )*\u221a\n                      <jats:styled-content style=\"fixed-case\">tPSA<\/jats:styled-content>\n                      ). The men's clinical information was used to derive their risk according to the Prostate Cancer Prevention Trial (\n                      <jats:styled-content style=\"fixed-case\">PCPT<\/jats:styled-content>\n                      ) risk model. Two clinical prediction models were created via multivariable regression consisting of age, family history, abnormality on digital rectal examination, previous negative biopsy and either\n                      <jats:styled-content style=\"fixed-case\">PSA<\/jats:styled-content>\n                      or\n                      <jats:styled-content style=\"fixed-case\">PHI<\/jats:styled-content>\n                      score, respectively. Calibration plots, receiver\u2010operating characteristic (\n                      <jats:styled-content style=\"fixed-case\">ROC<\/jats:styled-content>\n                      ) curves and decision curves were generated to assess the performance of the three\u00a0models.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      The\n                      <jats:styled-content style=\"fixed-case\">PSA<\/jats:styled-content>\n                      model and\n                      <jats:styled-content style=\"fixed-case\">PHI<\/jats:styled-content>\n                      model were both well calibrated in this cohort, with the\n                      <jats:styled-content style=\"fixed-case\">PHI<\/jats:styled-content>\n                      model showing the best correlation between predicted probabilities and actual outcome. The areas under the\n                      <jats:styled-content style=\"fixed-case\">ROC<\/jats:styled-content>\n                      curve for the\n                      <jats:styled-content style=\"fixed-case\">PHI<\/jats:styled-content>\n                      model,\n                      <jats:styled-content style=\"fixed-case\">PSA<\/jats:styled-content>\n                      model and\n                      <jats:styled-content style=\"fixed-case\">PCPT<\/jats:styled-content>\n                      model were 0.77, 0.71 and 0.69, respectively, for the prediction of prostate cancer (\n                      <jats:styled-content style=\"fixed-case\">PC<\/jats:styled-content>\n                      a) and 0.79, 0.72 and 0.72, respectively, for the prediction of high grade\n                      <jats:styled-content style=\"fixed-case\">PC<\/jats:styled-content>\n                      a. Decision\u2010curve analysis showed a superior net benefit of the\n                      <jats:styled-content style=\"fixed-case\">PHI<\/jats:styled-content>\n                      model over both the\n                      <jats:styled-content style=\"fixed-case\">PSA<\/jats:styled-content>\n                      model and the\n                      <jats:styled-content style=\"fixed-case\">PCPT<\/jats:styled-content>\n                      risk model in the diagnosis of\n                      <jats:styled-content style=\"fixed-case\">PC<\/jats:styled-content>\n                      a and high grade\n                      <jats:styled-content style=\"fixed-case\">PC<\/jats:styled-content>\n                      a over the entire range of risk probabilities.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>\n                      A logical and standardized approach to the use of clinical risk factors can allow more accurate risk stratification of men under investigation for\n                      <jats:styled-content style=\"fixed-case\">PC<\/jats:styled-content>\n                      a. The measurement of p2\n                      <jats:styled-content style=\"fixed-case\">PSA<\/jats:styled-content>\n                      and the integration of this biomarker into a clinical prediction model can further increase the accuracy of risk stratification, helping to better inform the decision for prostate biopsy in a referral population.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/bju.13143","type":"journal-article","created":{"date-parts":[[2015,4,3]],"date-time":"2015-04-03T14:07:54Z","timestamp":1428070074000},"page":"409-417","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":38,"title":["Improving multivariable prostate cancer risk assessment using the Prostate Health Index"],"prefix":"10.1111","volume":"117","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-5457-2392","authenticated-orcid":false,"given":"Robert W.","family":"Foley","sequence":"first","affiliation":[{"name":"Conway Institute of Biomolecular and Biomedical Research University College Dublin Dublin Ireland"},{"name":"UCD School of Medicine and Medical Science University College Dublin Dublin Ireland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Laura","family":"Gorman","sequence":"additional","affiliation":[{"name":"Conway Institute of Biomolecular and Biomedical Research University College Dublin Dublin Ireland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Neda","family":"Sharifi","sequence":"additional","affiliation":[{"name":"Department of Biochemistry Beaumont Hospital Dublin Ireland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Keefe","family":"Murphy","sequence":"additional","affiliation":[{"name":"UCD School of Mathematical Sciences University College Dublin Dublin Ireland"},{"name":"Insight Centre for Data Analytics University College Dublin Dublin Ireland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Helen","family":"Moore","sequence":"additional","affiliation":[{"name":"Department of Biochemistry Beaumont Hospital Dublin Ireland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alexandra V.","family":"Tuzova","sequence":"additional","affiliation":[{"name":"Prostate Molecular Oncology Institute of Molecular Medicine Trinity College Dublin Dublin Ireland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Antoinette S.","family":"Perry","sequence":"additional","affiliation":[{"name":"Prostate Molecular Oncology Institute of Molecular Medicine Trinity College Dublin Dublin Ireland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"T. 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