{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,19]],"date-time":"2026-08-19T20:06:01Z","timestamp":1787169961075,"version":"build-2736575974"},"reference-count":27,"publisher":"Wiley","issue":"6b","license":[{"start":{"date-parts":[[2014,4,29]],"date-time":"2014-04-29T00:00:00Z","timestamp":1398729600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["bjui-journals.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["BJU International"],"published-print":{"date-parts":[[2014,12]]},"abstract":"<jats:sec>\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>\n                      To evaluate the variability in prostate cancer gene 3 (\n                      <jats:styled-content style=\"fixed-case\">PCA3<\/jats:styled-content>\n                      ) score over time in men with elevated serum prostate\u2010specific antigen (\n                      <jats:styled-content style=\"fixed-case\">PSA<\/jats:styled-content>\n                      ) levels who are undergoing first or repeat prostate biopsy.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Patients and Methods<\/jats:title>\n                    <jats:p>\n                      A total of 360 men from two Italian institutions who had undergone at least two\n                      <jats:styled-content style=\"fixed-case\">PCA3<\/jats:styled-content>\n                      assessments were selected. Of these, 97.5% were scheduled for first or repeat prostate biopsy because of elevated\n                      <jats:styled-content style=\"fixed-case\">PSA<\/jats:styled-content>\n                      level and\/or positive digital rectal examination (\n                      <jats:styled-content style=\"fixed-case\">DRE<\/jats:styled-content>\n                      ). We compared the\n                      <jats:styled-content style=\"fixed-case\">PCA3<\/jats:styled-content>\n                      scores in men with a negative biopsy (normal parenchyma, benign prostatic hyperplasia [\n                      <jats:styled-content style=\"fixed-case\">BPH<\/jats:styled-content>\n                      ], chronic prostatitis, high\u2010grade prostate intraepithelial neoplasia [\n                      <jats:styled-content style=\"fixed-case\">HG\u2010PIN<\/jats:styled-content>\n                      ]) with those in men with a positive biopsy. We evaluated\n                      <jats:styled-content style=\"fixed-case\">PCA3<\/jats:styled-content>\n                      repeated measures biological variability and its possible association with basic patient characteristics (age, family history of prostate cancer,\n                      <jats:styled-content style=\"fixed-case\">DRE<\/jats:styled-content>\n                      , prostate volume,\n                      <jats:styled-content style=\"fixed-case\">BPH<\/jats:styled-content>\n                      , prostatitis and\n                      <jats:styled-content style=\"fixed-case\">HG\u2010PIN<\/jats:styled-content>\n                      ). Three different thresholds were used to evaluate the possible changes in risk class: the standard threshold (a\n                      <jats:styled-content style=\"fixed-case\">PCA3<\/jats:styled-content>\n                      score of 35), a\n                      <jats:styled-content style=\"fixed-case\">US F<\/jats:styled-content>\n                      ood and\n                      <jats:styled-content style=\"fixed-case\">D<\/jats:styled-content>\n                      rug\n                      <jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>\n                      dministation\u2010approved\n                      <jats:styled-content style=\"fixed-case\">PCA3<\/jats:styled-content>\n                      threshold of 25 and a threshold selected based on our previous research which was a\n                      <jats:styled-content style=\"fixed-case\">PCA3<\/jats:styled-content>\n                      score of 50.\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\">PCA3<\/jats:styled-content>\n                      scores varied significantly (\n                      <jats:italic>P<\/jats:italic>\n                      &lt; 0.001) when comparing men with a negative biopsy with those with a positive biopsy (median [range]\n                      <jats:styled-content style=\"fixed-case\">PCA3<\/jats:styled-content>\n                      score: 25 [2\u2013276] vs 43 [7\u2013331]). There was no significant difference in\n                      <jats:styled-content style=\"fixed-case\">PCA3<\/jats:styled-content>\n                      scores in men with chronic prostatitis and\n                      <jats:styled-content style=\"fixed-case\">HG\u2010PIN<\/jats:styled-content>\n                      compared with other men with negative biopsies. The median (range) time between the two\n                      <jats:styled-content style=\"fixed-case\">PCA3<\/jats:styled-content>\n                      assessments was 16.2 (3\u201353.7) months. No association was found between\n                      <jats:styled-content style=\"fixed-case\">PCA3<\/jats:styled-content>\n                      repeated measures modifications and age, family history of prostate cancer,\n                      <jats:styled-content style=\"fixed-case\">DRE<\/jats:styled-content>\n                      ,\n                      <jats:styled-content style=\"fixed-case\">BPH<\/jats:styled-content>\n                      , prostatitis,\n                      <jats:styled-content style=\"fixed-case\">HG\u2010PIN<\/jats:styled-content>\n                      and use of 5\u2010\u03b1\u2010reductase inhibitors. The variability of\n                      <jats:styled-content style=\"fixed-case\">PCA3<\/jats:styled-content>\n                      scores on repeated measures confirmed the risk class for about 80% of patients; of the remaining 20% of patients, the risk class was upgraded in two thirds and downgraded in one third.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>\n                      <jats:styled-content style=\"fixed-case\">PCA3<\/jats:styled-content>\n                      score can be considered a stable marker over time in most cases but there is a group of men among whom there is clinically notable risk class change. Further investigation is required to determine the genesis of this phenomenon.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/bju.12654","type":"journal-article","created":{"date-parts":[[2014,1,29]],"date-time":"2014-01-29T00:08:47Z","timestamp":1390954127000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":9,"title":["Fluctuation in prostate cancer gene 3 (\n                    <scp>PCA3<\/scp>\n                    ) score in men undergoing first or repeat prostate biopsies"],"prefix":"10.1111","volume":"114","author":[{"given":"Stefano","family":"De Luca","sequence":"first","affiliation":[{"name":"Department of Urology San Luigi Gonzaga Hospital  Orbassano Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Roberto","family":"Passera","sequence":"additional","affiliation":[{"name":"Department of Nuclear Medicine San Giovanni Battista Hospital  Torino Italy"},{"name":"University of Torino  Torino Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Susanna","family":"Cappia","sequence":"additional","affiliation":[{"name":"Department of Pathology San Luigi Gonzaga Hospital  Orbassano Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Enrico","family":"Bollito","sequence":"additional","affiliation":[{"name":"Department of Pathology San Luigi Gonzaga Hospital  Orbassano Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Donato Franco","family":"Randone","sequence":"additional","affiliation":[{"name":"Department of Urology Gradenigo Hospital  Torino Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Angela","family":"Milillo","sequence":"additional","affiliation":[{"name":"Department of Laboratory Medicine Gradenigo Hospital  Torino Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mauro","family":"Papotti","sequence":"additional","affiliation":[{"name":"Department of Pathology San Luigi Gonzaga Hospital  Orbassano Italy"},{"name":"University of Torino  Torino Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Francesco","family":"Porpiglia","sequence":"additional","affiliation":[{"name":"Department of Urology San Luigi Gonzaga Hospital  Orbassano Italy"},{"name":"University of Torino  Torino Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2014,4,29]]},"reference":[{"key":"e_1_2_6_2_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.juro.2009.07.093"},{"key":"e_1_2_6_3_1","first-page":"695","article-title":"DD3(PCA3), a very sensitive and specific marker to detect prostate tumors","volume":"62","author":"Kok JB","year":"2002","journal-title":"Cancer Res"},{"key":"e_1_2_6_4_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0090-4295(03)00759-3"},{"key":"e_1_2_6_5_1","first-page":"5975","article-title":"A new prostate\u2010specific gene, highly over expressed in prostate cancer","volume":"59","author":"Bussemakers MJ","year":"1999","journal-title":"Cancer Res"},{"key":"e_1_2_6_6_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.eururo.2008.06.043"},{"key":"e_1_2_6_7_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.ejca.2010.09.035"},{"key":"e_1_2_6_8_1","first-page":"243","volume-title":"UICC TNM Classification of Malignant Tumors","author":"Sobin LH","year":"2009"},{"key":"e_1_2_6_9_1","doi-asserted-by":"publisher","DOI":"10.1097\/01.pas.0000173646.99337.b1"},{"key":"e_1_2_6_10_1","first-page":"96","article-title":"Prostate cancer gene 3 urine assay cutoff in diagnosis of prostate cancer. 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