Preoperative Prostate-specific Antigen Isoform p2PSA and Its Derivatives, %p2PSA and Prostate Health Index, Predict Pathologic Outcomes in Patients Undergoing Radical Prostatectomy for Prostate Cancer: Results from a Multicentric European Prospective Study

Abstract Background Currently available predictive models fail to assist clinical decision making in prostate cancer (PCa) patients who are potential candidates for radical prostatectomy (RP). New biomarkers would be welcome. Objective To test the hypothesis that prostate-specific antigen (PSA) isof...

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Veröffentlicht in:European urology 2015-07, Vol.68 (1), p.132-138
Hauptverfasser: Fossati, Nicola, Buffi, Nicolò Maria, Haese, Alexander, Stephan, Carsten, Larcher, Alessandro, McNicholas, Thomas, de la Taille, Alexandre, Freschi, Massimo, Lughezzani, Giovanni, Abrate, Alberto, Bini, Vittorio, Palou Redorta, Joan, Graefen, Markus, Guazzoni, Giorgio, Lazzeri, Massimo
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container_end_page 138
container_issue 1
container_start_page 132
container_title European urology
container_volume 68
creator Fossati, Nicola
Buffi, Nicolò Maria
Haese, Alexander
Stephan, Carsten
Larcher, Alessandro
McNicholas, Thomas
de la Taille, Alexandre
Freschi, Massimo
Lughezzani, Giovanni
Abrate, Alberto
Bini, Vittorio
Palou Redorta, Joan
Graefen, Markus
Guazzoni, Giorgio
Lazzeri, Massimo
description Abstract Background Currently available predictive models fail to assist clinical decision making in prostate cancer (PCa) patients who are potential candidates for radical prostatectomy (RP). New biomarkers would be welcome. Objective To test the hypothesis that prostate-specific antigen (PSA) isoform p2PSA and its derivatives, percentage of p2PSA to free PSA (%p2PSA) and the Prostate Health Index (PHI), predict PCa characteristics at final pathology. Design, setting, and participants An observational prospective multicentre European study was performed in 489 consecutive PCa patients treated with RP. Total PSA (tPSA), free PSA (fPSA), and p2PSA levels were determined. The %fPSA [(fPSA / tPSA) × 100], %p2PSA [(p2PSA pg/ml) / (fPSA ng/ml × 1000) × 100], and PHI [(p2PSA / fPSA) × √tPSA] were calculated. Intervention Open or robot-assisted RP. Outcome measurements and statistical analysis Logistic regression models were fitted to test the predictors of pT3 stage and/or pathologic Gleason score (GS) ≥7 and to determine their predictive accuracy. The base multivariable model included tPSA, digital rectal examination, biopsy GS, and percentage of positive biopsy cores. Decision curve analysis provided an estimate of the net benefit obtained using p2PSA, %p2PSA, or PHI. Results and limitations Overall, 344 patients (70%) were affected by pT3 disease or pathologic GS ≥7; pT3 disease and pathologic GS ≥7 were present in 126 patients (26%). At univariable analysis, p2PSA, %p2PSA, and PHI were significant predictors of pT3 disease and/or pathologic GS ≥7 (all p ≤ 0.001). The inclusion of PHI significantly increased the accuracy of the base multivariable model by 2.3% ( p = 0.003) and 2.4% ( p = 0.01) for the prediction of pT3 disease and/or pathologic GS ≥7, respectively. However, at decision curve analysis, models including PHI did not show evidence of a greater clinical net benefit. Conclusions Both %p2PSA and PHI are significant predictors of unfavourable PCa characteristics at final pathology; however, %p2PSA and PHI did not provide a greater net benefit for clinical decision making. Patient summary Prostate-specific antigen (PSA) isoform p2PSA and its derivatives, percentage of p2PSA to free PSA and the Prostate Health Index, are associated with adverse characteristics of prostate cancer; however, these biomarkers provided only a slight net benefit for clinical decision making.
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New biomarkers would be welcome. Objective To test the hypothesis that prostate-specific antigen (PSA) isoform p2PSA and its derivatives, percentage of p2PSA to free PSA (%p2PSA) and the Prostate Health Index (PHI), predict PCa characteristics at final pathology. Design, setting, and participants An observational prospective multicentre European study was performed in 489 consecutive PCa patients treated with RP. Total PSA (tPSA), free PSA (fPSA), and p2PSA levels were determined. The %fPSA [(fPSA / tPSA) × 100], %p2PSA [(p2PSA pg/ml) / (fPSA ng/ml × 1000) × 100], and PHI [(p2PSA / fPSA) × √tPSA] were calculated. Intervention Open or robot-assisted RP. Outcome measurements and statistical analysis Logistic regression models were fitted to test the predictors of pT3 stage and/or pathologic Gleason score (GS) ≥7 and to determine their predictive accuracy. The base multivariable model included tPSA, digital rectal examination, biopsy GS, and percentage of positive biopsy cores. Decision curve analysis provided an estimate of the net benefit obtained using p2PSA, %p2PSA, or PHI. Results and limitations Overall, 344 patients (70%) were affected by pT3 disease or pathologic GS ≥7; pT3 disease and pathologic GS ≥7 were present in 126 patients (26%). At univariable analysis, p2PSA, %p2PSA, and PHI were significant predictors of pT3 disease and/or pathologic GS ≥7 (all p ≤ 0.001). The inclusion of PHI significantly increased the accuracy of the base multivariable model by 2.3% ( p = 0.003) and 2.4% ( p = 0.01) for the prediction of pT3 disease and/or pathologic GS ≥7, respectively. However, at decision curve analysis, models including PHI did not show evidence of a greater clinical net benefit. Conclusions Both %p2PSA and PHI are significant predictors of unfavourable PCa characteristics at final pathology; however, %p2PSA and PHI did not provide a greater net benefit for clinical decision making. Patient summary Prostate-specific antigen (PSA) isoform p2PSA and its derivatives, percentage of p2PSA to free PSA and the Prostate Health Index, are associated with adverse characteristics of prostate cancer; however, these biomarkers provided only a slight net benefit for clinical decision making.</description><identifier>ISSN: 0302-2838</identifier><identifier>EISSN: 1873-7560</identifier><identifier>DOI: 10.1016/j.eururo.2014.07.034</identifier><identifier>PMID: 25139197</identifier><language>eng</language><publisher>Switzerland: Elsevier B.V</publisher><subject>Aged ; Biomarkers ; Biomarkers, Tumor - metabolism ; Cohort Studies ; Humans ; Kallikreins - metabolism ; Logistic Models ; Lymph Nodes - pathology ; Male ; Middle Aged ; Neoplasm Grading ; Neoplasm Staging ; p2PSA ; Pathologic outcomes ; Predictive models ; Prognosis ; Prospective Studies ; Prostate cancer ; Prostate Health Index ; Prostate-Specific Antigen - metabolism ; Prostatectomy ; Prostatic Neoplasms - metabolism ; Prostatic Neoplasms - pathology ; Prostatic Neoplasms - surgery ; Protein Precursors - metabolism ; Urology</subject><ispartof>European urology, 2015-07, Vol.68 (1), p.132-138</ispartof><rights>European Association of Urology</rights><rights>2014 European Association of Urology</rights><rights>Copyright © 2014 European Association of Urology. Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c487t-5872c47430066b10cad2aab041de70bd8deea50ffb54983e73a2f9495611200c3</citedby><cites>FETCH-LOGICAL-c487t-5872c47430066b10cad2aab041de70bd8deea50ffb54983e73a2f9495611200c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0302283814006861$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25139197$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fossati, Nicola</creatorcontrib><creatorcontrib>Buffi, Nicolò Maria</creatorcontrib><creatorcontrib>Haese, Alexander</creatorcontrib><creatorcontrib>Stephan, Carsten</creatorcontrib><creatorcontrib>Larcher, Alessandro</creatorcontrib><creatorcontrib>McNicholas, Thomas</creatorcontrib><creatorcontrib>de la Taille, Alexandre</creatorcontrib><creatorcontrib>Freschi, Massimo</creatorcontrib><creatorcontrib>Lughezzani, Giovanni</creatorcontrib><creatorcontrib>Abrate, Alberto</creatorcontrib><creatorcontrib>Bini, Vittorio</creatorcontrib><creatorcontrib>Palou Redorta, Joan</creatorcontrib><creatorcontrib>Graefen, Markus</creatorcontrib><creatorcontrib>Guazzoni, Giorgio</creatorcontrib><creatorcontrib>Lazzeri, Massimo</creatorcontrib><title>Preoperative Prostate-specific Antigen Isoform p2PSA and Its Derivatives, %p2PSA and Prostate Health Index, Predict Pathologic Outcomes in Patients Undergoing Radical Prostatectomy for Prostate Cancer: Results from a Multicentric European Prospective Study</title><title>European urology</title><addtitle>Eur Urol</addtitle><description>Abstract Background Currently available predictive models fail to assist clinical decision making in prostate cancer (PCa) patients who are potential candidates for radical prostatectomy (RP). New biomarkers would be welcome. Objective To test the hypothesis that prostate-specific antigen (PSA) isoform p2PSA and its derivatives, percentage of p2PSA to free PSA (%p2PSA) and the Prostate Health Index (PHI), predict PCa characteristics at final pathology. Design, setting, and participants An observational prospective multicentre European study was performed in 489 consecutive PCa patients treated with RP. Total PSA (tPSA), free PSA (fPSA), and p2PSA levels were determined. The %fPSA [(fPSA / tPSA) × 100], %p2PSA [(p2PSA pg/ml) / (fPSA ng/ml × 1000) × 100], and PHI [(p2PSA / fPSA) × √tPSA] were calculated. Intervention Open or robot-assisted RP. Outcome measurements and statistical analysis Logistic regression models were fitted to test the predictors of pT3 stage and/or pathologic Gleason score (GS) ≥7 and to determine their predictive accuracy. The base multivariable model included tPSA, digital rectal examination, biopsy GS, and percentage of positive biopsy cores. Decision curve analysis provided an estimate of the net benefit obtained using p2PSA, %p2PSA, or PHI. Results and limitations Overall, 344 patients (70%) were affected by pT3 disease or pathologic GS ≥7; pT3 disease and pathologic GS ≥7 were present in 126 patients (26%). At univariable analysis, p2PSA, %p2PSA, and PHI were significant predictors of pT3 disease and/or pathologic GS ≥7 (all p ≤ 0.001). The inclusion of PHI significantly increased the accuracy of the base multivariable model by 2.3% ( p = 0.003) and 2.4% ( p = 0.01) for the prediction of pT3 disease and/or pathologic GS ≥7, respectively. However, at decision curve analysis, models including PHI did not show evidence of a greater clinical net benefit. Conclusions Both %p2PSA and PHI are significant predictors of unfavourable PCa characteristics at final pathology; however, %p2PSA and PHI did not provide a greater net benefit for clinical decision making. Patient summary Prostate-specific antigen (PSA) isoform p2PSA and its derivatives, percentage of p2PSA to free PSA and the Prostate Health Index, are associated with adverse characteristics of prostate cancer; however, these biomarkers provided only a slight net benefit for clinical decision making.</description><subject>Aged</subject><subject>Biomarkers</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Cohort Studies</subject><subject>Humans</subject><subject>Kallikreins - metabolism</subject><subject>Logistic Models</subject><subject>Lymph Nodes - pathology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neoplasm Grading</subject><subject>Neoplasm Staging</subject><subject>p2PSA</subject><subject>Pathologic outcomes</subject><subject>Predictive models</subject><subject>Prognosis</subject><subject>Prospective Studies</subject><subject>Prostate cancer</subject><subject>Prostate Health Index</subject><subject>Prostate-Specific Antigen - metabolism</subject><subject>Prostatectomy</subject><subject>Prostatic Neoplasms - metabolism</subject><subject>Prostatic Neoplasms - pathology</subject><subject>Prostatic Neoplasms - surgery</subject><subject>Protein Precursors - metabolism</subject><subject>Urology</subject><issn>0302-2838</issn><issn>1873-7560</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUk1vEzEQXRCIhsI_QMgXJA7dYK_3kwNSlBYaqahRQ8-W451NHXbtxfZG5N93NumHxIWTZfu9NzPvTRR9YHTKKMu_bKcwuMHZaUJZOqXFlPL0ZTRhZcHjIsvpq2hCOU3ipOTlSfTW-y2llGcVfxOdJBnjFauKyYto6cD24GTQOyBLZ32QAWLfg9KNVmRmgt6AIQtvG-s60ifL1YxIU5NF8OQcnN4dqP6MfHr-e9QhlyDbcEcWpoa_Z_gMtVaBLGW4s63doP71EJTtwBNtxmcNBmVvEe42VpsNuZHIkO2Togq22xNs5bnGXBoF7iu5AT-0yG6c7YgkP_GiFeo5LHOBRvUgzYGFsx2mXYWh3r-LXjey9fD-4TyNbr9f_JpfxlfXPxbz2VWs0rIIcVYWiUqLlFOa52tGlawTKdc0ZTUUdF2XNYDMaNOss7QqORRcJk2VVlnOWEKp4qfR56Nu7-yfAXwQnfYK2lYasIMXLK9owljKM4SmR6jCZr2DRvROd9LtBaNizF5sxTF7MWYvaCEwe6R9fKgwrDuon0iPYSPg2xEAOOdOgxNeoeEKQ3Foiait_l-FfwVUq82Yz2_Yg9_awRn0UDDhE0HFaty_cf1Yiq6VOeP3t1nbpQ</recordid><startdate>20150701</startdate><enddate>20150701</enddate><creator>Fossati, Nicola</creator><creator>Buffi, Nicolò Maria</creator><creator>Haese, Alexander</creator><creator>Stephan, Carsten</creator><creator>Larcher, Alessandro</creator><creator>McNicholas, Thomas</creator><creator>de la Taille, Alexandre</creator><creator>Freschi, Massimo</creator><creator>Lughezzani, Giovanni</creator><creator>Abrate, Alberto</creator><creator>Bini, Vittorio</creator><creator>Palou Redorta, Joan</creator><creator>Graefen, Markus</creator><creator>Guazzoni, Giorgio</creator><creator>Lazzeri, Massimo</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20150701</creationdate><title>Preoperative Prostate-specific Antigen Isoform p2PSA and Its Derivatives, %p2PSA and Prostate Health Index, Predict Pathologic Outcomes in Patients Undergoing Radical Prostatectomy for Prostate Cancer: Results from a Multicentric European Prospective Study</title><author>Fossati, Nicola ; Buffi, Nicolò Maria ; Haese, Alexander ; Stephan, Carsten ; Larcher, Alessandro ; McNicholas, Thomas ; de la Taille, Alexandre ; Freschi, Massimo ; Lughezzani, Giovanni ; Abrate, Alberto ; Bini, Vittorio ; Palou Redorta, Joan ; Graefen, Markus ; Guazzoni, Giorgio ; Lazzeri, Massimo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c487t-5872c47430066b10cad2aab041de70bd8deea50ffb54983e73a2f9495611200c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Aged</topic><topic>Biomarkers</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>Cohort Studies</topic><topic>Humans</topic><topic>Kallikreins - metabolism</topic><topic>Logistic Models</topic><topic>Lymph Nodes - pathology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neoplasm Grading</topic><topic>Neoplasm Staging</topic><topic>p2PSA</topic><topic>Pathologic outcomes</topic><topic>Predictive models</topic><topic>Prognosis</topic><topic>Prospective Studies</topic><topic>Prostate cancer</topic><topic>Prostate Health Index</topic><topic>Prostate-Specific Antigen - metabolism</topic><topic>Prostatectomy</topic><topic>Prostatic Neoplasms - metabolism</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Prostatic Neoplasms - surgery</topic><topic>Protein Precursors - metabolism</topic><topic>Urology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fossati, Nicola</creatorcontrib><creatorcontrib>Buffi, Nicolò Maria</creatorcontrib><creatorcontrib>Haese, Alexander</creatorcontrib><creatorcontrib>Stephan, Carsten</creatorcontrib><creatorcontrib>Larcher, Alessandro</creatorcontrib><creatorcontrib>McNicholas, Thomas</creatorcontrib><creatorcontrib>de la Taille, Alexandre</creatorcontrib><creatorcontrib>Freschi, Massimo</creatorcontrib><creatorcontrib>Lughezzani, Giovanni</creatorcontrib><creatorcontrib>Abrate, Alberto</creatorcontrib><creatorcontrib>Bini, Vittorio</creatorcontrib><creatorcontrib>Palou Redorta, Joan</creatorcontrib><creatorcontrib>Graefen, Markus</creatorcontrib><creatorcontrib>Guazzoni, Giorgio</creatorcontrib><creatorcontrib>Lazzeri, Massimo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European urology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fossati, Nicola</au><au>Buffi, Nicolò Maria</au><au>Haese, Alexander</au><au>Stephan, Carsten</au><au>Larcher, Alessandro</au><au>McNicholas, Thomas</au><au>de la Taille, Alexandre</au><au>Freschi, Massimo</au><au>Lughezzani, Giovanni</au><au>Abrate, Alberto</au><au>Bini, Vittorio</au><au>Palou Redorta, Joan</au><au>Graefen, Markus</au><au>Guazzoni, Giorgio</au><au>Lazzeri, Massimo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preoperative Prostate-specific Antigen Isoform p2PSA and Its Derivatives, %p2PSA and Prostate Health Index, Predict Pathologic Outcomes in Patients Undergoing Radical Prostatectomy for Prostate Cancer: Results from a Multicentric European Prospective Study</atitle><jtitle>European urology</jtitle><addtitle>Eur Urol</addtitle><date>2015-07-01</date><risdate>2015</risdate><volume>68</volume><issue>1</issue><spage>132</spage><epage>138</epage><pages>132-138</pages><issn>0302-2838</issn><eissn>1873-7560</eissn><abstract>Abstract Background Currently available predictive models fail to assist clinical decision making in prostate cancer (PCa) patients who are potential candidates for radical prostatectomy (RP). New biomarkers would be welcome. Objective To test the hypothesis that prostate-specific antigen (PSA) isoform p2PSA and its derivatives, percentage of p2PSA to free PSA (%p2PSA) and the Prostate Health Index (PHI), predict PCa characteristics at final pathology. Design, setting, and participants An observational prospective multicentre European study was performed in 489 consecutive PCa patients treated with RP. Total PSA (tPSA), free PSA (fPSA), and p2PSA levels were determined. The %fPSA [(fPSA / tPSA) × 100], %p2PSA [(p2PSA pg/ml) / (fPSA ng/ml × 1000) × 100], and PHI [(p2PSA / fPSA) × √tPSA] were calculated. Intervention Open or robot-assisted RP. Outcome measurements and statistical analysis Logistic regression models were fitted to test the predictors of pT3 stage and/or pathologic Gleason score (GS) ≥7 and to determine their predictive accuracy. The base multivariable model included tPSA, digital rectal examination, biopsy GS, and percentage of positive biopsy cores. Decision curve analysis provided an estimate of the net benefit obtained using p2PSA, %p2PSA, or PHI. Results and limitations Overall, 344 patients (70%) were affected by pT3 disease or pathologic GS ≥7; pT3 disease and pathologic GS ≥7 were present in 126 patients (26%). At univariable analysis, p2PSA, %p2PSA, and PHI were significant predictors of pT3 disease and/or pathologic GS ≥7 (all p ≤ 0.001). The inclusion of PHI significantly increased the accuracy of the base multivariable model by 2.3% ( p = 0.003) and 2.4% ( p = 0.01) for the prediction of pT3 disease and/or pathologic GS ≥7, respectively. However, at decision curve analysis, models including PHI did not show evidence of a greater clinical net benefit. Conclusions Both %p2PSA and PHI are significant predictors of unfavourable PCa characteristics at final pathology; however, %p2PSA and PHI did not provide a greater net benefit for clinical decision making. Patient summary Prostate-specific antigen (PSA) isoform p2PSA and its derivatives, percentage of p2PSA to free PSA and the Prostate Health Index, are associated with adverse characteristics of prostate cancer; however, these biomarkers provided only a slight net benefit for clinical decision making.</abstract><cop>Switzerland</cop><pub>Elsevier B.V</pub><pmid>25139197</pmid><doi>10.1016/j.eururo.2014.07.034</doi><tpages>7</tpages></addata></record>
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subjects Aged
Biomarkers
Biomarkers, Tumor - metabolism
Cohort Studies
Humans
Kallikreins - metabolism
Logistic Models
Lymph Nodes - pathology
Male
Middle Aged
Neoplasm Grading
Neoplasm Staging
p2PSA
Pathologic outcomes
Predictive models
Prognosis
Prospective Studies
Prostate cancer
Prostate Health Index
Prostate-Specific Antigen - metabolism
Prostatectomy
Prostatic Neoplasms - metabolism
Prostatic Neoplasms - pathology
Prostatic Neoplasms - surgery
Protein Precursors - metabolism
Urology
title Preoperative Prostate-specific Antigen Isoform p2PSA and Its Derivatives, %p2PSA and Prostate Health Index, Predict Pathologic Outcomes in Patients Undergoing Radical Prostatectomy for Prostate Cancer: Results from a Multicentric European Prospective Study
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