{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,19]],"date-time":"2025-12-19T21:46:47Z","timestamp":1766180807454,"version":"build-2065373602"},"reference-count":28,"publisher":"Wiley","issue":"S3","license":[{"start":{"date-parts":[[2015,7,27]],"date-time":"2015-07-27T00:00:00Z","timestamp":1437955200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"name":"The Royal College of Pathologists of Australia"}],"content-domain":{"domain":["bjui-journals.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["BJU International"],"published-print":{"date-parts":[[2015,10]]},"abstract":"<jats:sec>\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>\n                      To assess the influence of tumour zonality on biochemical recurrence (\n                      <jats:styled-content style=\"fixed-case\">BCR<\/jats:styled-content>\n                      ) after radical prostatectomy (\n                      <jats:styled-content style=\"fixed-case\">RP<\/jats:styled-content>\n                      ) with a histologically confirmed positive surgical margin (\n                      <jats:styled-content style=\"fixed-case\">PSM<\/jats:styled-content>\n                      ).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Patients and Methods<\/jats:title>\n                    <jats:p>\n                      Data from 382 patients that underwent\n                      <jats:styled-content style=\"fixed-case\">RP<\/jats:styled-content>\n                      with either transition zone (\n                      <jats:styled-content style=\"fixed-case\">TZ<\/jats:styled-content>\n                      ) or peripheral zone (\n                      <jats:styled-content style=\"fixed-case\">PZ<\/jats:styled-content>\n                      ) tumours involving\n                      <jats:styled-content style=\"fixed-case\">PSMs<\/jats:styled-content>\n                      between 1998 and 2010 were retrieved from the\n                      <jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>\n                      bbott\n                      <jats:styled-content style=\"fixed-case\">W<\/jats:styled-content>\n                      est\n                      <jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>\n                      ustralian\n                      <jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>\n                      rostatectomy\n                      <jats:styled-content style=\"fixed-case\">D<\/jats:styled-content>\n                      atabase. Statistical analysis was used to evaluate the relationship of various tumour clinicopathological parameters, e.g. zonal origin of tumour, tumour volume,\n                      <jats:styled-content style=\"fixed-case\">G<\/jats:styled-content>\n                      leason score, and stage to the development of\n                      <jats:styled-content style=\"fixed-case\">BCR<\/jats:styled-content>\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      There were 51\n                      <jats:styled-content style=\"fixed-case\">TZ<\/jats:styled-content>\n                      and 331\n                      <jats:styled-content style=\"fixed-case\">PZ<\/jats:styled-content>\n                      tumours with\n                      <jats:styled-content style=\"fixed-case\">PSMs<\/jats:styled-content>\n                      identified. The\n                      <jats:styled-content style=\"fixed-case\">TZ<\/jats:styled-content>\n                      tumours compared with\n                      <jats:styled-content style=\"fixed-case\">PZ<\/jats:styled-content>\n                      tumours were larger (median 5.67 vs 3.64\u2009mL,\n                      <jats:italic>P<\/jats:italic>\n                      &lt; 0.001), more frequently lower grade (\n                      <jats:styled-content style=\"fixed-case\">G<\/jats:styled-content>\n                      leason score 6 33% vs 5%,\n                      <jats:italic>P<\/jats:italic>\n                      &lt; 0.01), organ confined (51% vs 35.6%,\n                      <jats:italic>P<\/jats:italic>\n                      = 0.073), and preferentially involved the bladder neck (49% vs 6%,\n                      <jats:italic>P<\/jats:italic>\n                      &lt; 0.001). Tumour zonality was not associated with\n                      <jats:styled-content style=\"fixed-case\">BCR<\/jats:styled-content>\n                      for the entire cohort.\n                      <jats:styled-content style=\"fixed-case\">TZ<\/jats:styled-content>\n                      and\n                      <jats:styled-content style=\"fixed-case\">PZ<\/jats:styled-content>\n                      tumours had similar 5\u2010year\n                      <jats:styled-content style=\"fixed-case\">BCR<\/jats:styled-content>\n                      \u2010free survival rates (58% vs 63%,\n                      <jats:italic>P<\/jats:italic>\n                      = 0.691) and comparable time to development of\n                      <jats:styled-content style=\"fixed-case\">BCR<\/jats:styled-content>\n                      (14.4 vs 19.2 months,\n                      <jats:italic>P<\/jats:italic>\n                      = 0.346). On univariate analysis, preoperative\n                      <jats:styled-content style=\"fixed-case\">PSA<\/jats:styled-content>\n                      level,\n                      <jats:styled-content style=\"fixed-case\">PSM<\/jats:styled-content>\n                      at the bladder neck, tumour volume,\n                      <jats:styled-content style=\"fixed-case\">G<\/jats:styled-content>\n                      leason score (\n                      <jats:italic>P<\/jats:italic>\n                      &lt; 0.001) and tumour stage were independent predictors of\n                      <jats:styled-content style=\"fixed-case\">BCR<\/jats:styled-content>\n                      for the entire cohort. On multivariate analysis tumour volume and\n                      <jats:styled-content style=\"fixed-case\">G<\/jats:styled-content>\n                      leason score retained significance as independent predictors of\n                      <jats:styled-content style=\"fixed-case\">BCR<\/jats:styled-content>\n                      . Tumour zonality was not directly associated with\n                      <jats:styled-content style=\"fixed-case\">BCR<\/jats:styled-content>\n                      . Of the patients who received adjuvant therapy, the incidence of\n                      <jats:styled-content style=\"fixed-case\">BCR<\/jats:styled-content>\n                      was similar for\n                      <jats:styled-content style=\"fixed-case\">TZ<\/jats:styled-content>\n                      and\n                      <jats:styled-content style=\"fixed-case\">PZ<\/jats:styled-content>\n                      tumours (58% vs 67%,\n                      <jats:italic>P<\/jats:italic>\n                      = 0.077), although\n                      <jats:styled-content style=\"fixed-case\">TZ<\/jats:styled-content>\n                      tumours failed significantly earlier (mean 4.4 vs 16.4 months,\n                      <jats:italic>P<\/jats:italic>\n                      = 0.037).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      <jats:styled-content style=\"fixed-case\">PSA<\/jats:styled-content>\n                      recurrence in patients with histologically confirmed\n                      <jats:styled-content style=\"fixed-case\">PSMs<\/jats:styled-content>\n                      after\n                      <jats:styled-content style=\"fixed-case\">RP<\/jats:styled-content>\n                      is independent of the zonal location of the index tumour. However, tumour zonal origin may have an indirect influence on\n                      <jats:styled-content style=\"fixed-case\">PSA<\/jats:styled-content>\n                      relapse, as\n                      <jats:styled-content style=\"fixed-case\">TZ<\/jats:styled-content>\n                      tumours tend to be of large volume and more likely involve the bladder neck margin, both risk factors for\n                      <jats:styled-content style=\"fixed-case\">BCR<\/jats:styled-content>\n                      . Bladder neck margin involvement is associated with higher rates of\n                      <jats:styled-content style=\"fixed-case\">BCR<\/jats:styled-content>\n                      than other sites of\n                      <jats:styled-content style=\"fixed-case\">PSMs<\/jats:styled-content>\n                      . The preoperative identification of\n                      <jats:styled-content style=\"fixed-case\">TZ<\/jats:styled-content>\n                      tumours might aid surgical planning with appropriate alteration of\n                      <jats:styled-content style=\"fixed-case\">RP<\/jats:styled-content>\n                      technique to incorporate wider surgical margins at the bladder neck. Adjuvant radiotherapy appears to be associated with adverse outcome for\n                      <jats:styled-content style=\"fixed-case\">TZ<\/jats:styled-content>\n                      tumours, a novel finding which warrants further investigation.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/bju.13173","type":"journal-article","created":{"date-parts":[[2015,7,27]],"date-time":"2015-07-27T06:12:57Z","timestamp":1437977577000},"page":"42-48","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":16,"title":["Prostate carcinoma with positive margins at radical prostatectomy: role of tumour zonal origin in biochemical recurrence"],"prefix":"10.1111","volume":"116","author":[{"given":"Luke M.","family":"O'Neil","sequence":"first","affiliation":[{"name":"School of Medicine University of Notre Dame  Fremantle Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shane","family":"Walsh","sequence":"additional","affiliation":[{"name":"Uropath Pty Ltd  Perth Western Australia Australia"},{"name":"West Australian Urologic Research Organisation  Perth Western Australia Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ronald J.","family":"Cohen","sequence":"additional","affiliation":[{"name":"Uropath Pty Ltd  Perth Western Australia Australia"},{"name":"School of Pathology and Laboratory Medicine Faculty of Medicine and Dentistry University of Western Australia  Perth Western Australia Australia"},{"name":"West Australian Urologic Research Organisation  Perth Western Australia Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Stephen","family":"Lee","sequence":"additional","affiliation":[{"name":"Uropath Pty Ltd  Perth Western Australia Australia"},{"name":"School of Pathology and Laboratory Medicine Faculty of Medicine and 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