Serum insulin-like growth factor I/free prostate specific antigen (IGF-I/fPSA) ratio enhances prostate cancer detection in men with total PSA 4.0-10.0 ng/ml

Background Recent studies have suggested that IGF‐I and IGFBP‐3, in combination with PSA, may enhance PCa detection. This study was to investigate the use of serum IGF‐I and IGFBP‐3, and their combinations with prostate volume and fPSA in enhancing the discriminatory diagnosis of PCa in men with tPS...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of surgical oncology 2007-07, Vol.96 (1), p.54-61
Hauptverfasser: Zhigang, Zhao, Jieming, Liu, Su, Li, Wenlu, Shen
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 61
container_issue 1
container_start_page 54
container_title Journal of surgical oncology
container_volume 96
creator Zhigang, Zhao
Jieming, Liu
Su, Li
Wenlu, Shen
description Background Recent studies have suggested that IGF‐I and IGFBP‐3, in combination with PSA, may enhance PCa detection. This study was to investigate the use of serum IGF‐I and IGFBP‐3, and their combinations with prostate volume and fPSA in enhancing the discriminatory diagnosis of PCa in men with tPSA of 4.0–10.0 ng/ml. Methods Serum IGF‐I and IGFBP‐3 were determined by ELISA from 586 men with tPSA between 4.0 and 10.0 ng/ml. Of them, 281 were diagnosed with PCa and 305 without. ROC, univariate and multivariate logistic regression analyses were performed to evaluate the predictive performance of those parameters. Results IGF‐I, IGFD, IGF‐I/fPSA, and IGFBP‐3/fPSA were significantly higher in PCa cases than benign controls, whereas the differences of IGFBP‐3 and IGFBPD were statistically insignificant between the two groups, respectively. The AUC values indicated enhanced performance of IGF‐I/fPSA ratio (AUC = 0.753) in PCa detection compared with the currently used f/tPSA (AUC = 0.689). Multivariate logistic regression confirmed the observed relationships and identified IGF‐I/fPSA as independent factor in PCa presence. Conclusion Our data show that IGF‐I/fPSA as a promising marker can enhance PCa detection in ambiguous cases often found in the tPSA between 4.0 and 10.0 ng/ml. J. Surg. Oncol. 2007;96:54–61. © 2007 Wiley‐Liss, Inc.
doi_str_mv 10.1002/jso.20784
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_70684189</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>70684189</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3614-1ca9b8f3e89901a3640ede46b70475fa4e5fac045eb6c02b61489ccd1af2886c3</originalsourceid><addsrcrecordid>eNp1kc9uEzEQhy0EoqFw4AWQT4geNhnver32sSo0BFW0UkBIuVheZzZ1u39S26u079KHxSWBnrjYsvx9v_F4CHnPYMoA8tlNGKY5VJK_IBMGSmQKlHxJJukuz3il4Ii8CeEGAJQS_DU5YlXBy1IVE_K4RD921PVhbF2fte4W6cYPu3hNG2Pj4Oli1nhEuvVDiCYiDVu0rnGWmj66Dfb002J-niXqanl6Qr2JbqDYX5veYni27NPZ0zVGtInoU0XaJXnnUqU4RNPS5FM-hSx1BbTfzLr2LXnVmDbgu8N-TH6ef_lx9jW7uJwvzk4vMlsIxjNmjaplU6BUCpgpBAdcIxd1BbwqG8MxLRZ4ibWwkNfJkcraNTNNLqWwxTH5uM9Nz70bMUTduWCxbU2Pwxh0BUJyJlUCT_agTX0Fj43eetcZ_6AZ6KdR6DQK_WcUif1wCB3rDtfP5OHvEzDbAzvX4sP_k_S35eXfyGxvuBDx_p9h_K0WVVGV-tf3uV6t2Ge5XK30VfEb7KaiUg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>70684189</pqid></control><display><type>article</type><title>Serum insulin-like growth factor I/free prostate specific antigen (IGF-I/fPSA) ratio enhances prostate cancer detection in men with total PSA 4.0-10.0 ng/ml</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Zhigang, Zhao ; Jieming, Liu ; Su, Li ; Wenlu, Shen</creator><creatorcontrib>Zhigang, Zhao ; Jieming, Liu ; Su, Li ; Wenlu, Shen</creatorcontrib><description>Background Recent studies have suggested that IGF‐I and IGFBP‐3, in combination with PSA, may enhance PCa detection. This study was to investigate the use of serum IGF‐I and IGFBP‐3, and their combinations with prostate volume and fPSA in enhancing the discriminatory diagnosis of PCa in men with tPSA of 4.0–10.0 ng/ml. Methods Serum IGF‐I and IGFBP‐3 were determined by ELISA from 586 men with tPSA between 4.0 and 10.0 ng/ml. Of them, 281 were diagnosed with PCa and 305 without. ROC, univariate and multivariate logistic regression analyses were performed to evaluate the predictive performance of those parameters. Results IGF‐I, IGFD, IGF‐I/fPSA, and IGFBP‐3/fPSA were significantly higher in PCa cases than benign controls, whereas the differences of IGFBP‐3 and IGFBPD were statistically insignificant between the two groups, respectively. The AUC values indicated enhanced performance of IGF‐I/fPSA ratio (AUC = 0.753) in PCa detection compared with the currently used f/tPSA (AUC = 0.689). Multivariate logistic regression confirmed the observed relationships and identified IGF‐I/fPSA as independent factor in PCa presence. Conclusion Our data show that IGF‐I/fPSA as a promising marker can enhance PCa detection in ambiguous cases often found in the tPSA between 4.0 and 10.0 ng/ml. J. Surg. Oncol. 2007;96:54–61. © 2007 Wiley‐Liss, Inc.</description><identifier>ISSN: 0022-4790</identifier><identifier>EISSN: 1096-9098</identifier><identifier>DOI: 10.1002/jso.20784</identifier><identifier>PMID: 17345593</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Aged ; Biomarkers, Tumor - blood ; Humans ; insulin-like growth factor binding protein 3 (IGFBP-3) ; Insulin-Like Growth Factor Binding Protein 3 - blood ; insulin-like growth factor I (IGF-I) ; Insulin-Like Growth Factor I - analysis ; Logistic Models ; Male ; Middle Aged ; Multivariate Analysis ; prostate carcinoma (PCa) ; prostate specific antigen (PSA) ; Prostate-Specific Antigen - blood ; Prostatic Neoplasms - diagnosis ; ROC Curve ; Sensitivity and Specificity</subject><ispartof>Journal of surgical oncology, 2007-07, Vol.96 (1), p.54-61</ispartof><rights>Copyright © 2007 Wiley‐Liss, Inc.</rights><rights>Copyright 2007 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3614-1ca9b8f3e89901a3640ede46b70475fa4e5fac045eb6c02b61489ccd1af2886c3</citedby><cites>FETCH-LOGICAL-c3614-1ca9b8f3e89901a3640ede46b70475fa4e5fac045eb6c02b61489ccd1af2886c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjso.20784$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjso.20784$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17345593$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhigang, Zhao</creatorcontrib><creatorcontrib>Jieming, Liu</creatorcontrib><creatorcontrib>Su, Li</creatorcontrib><creatorcontrib>Wenlu, Shen</creatorcontrib><title>Serum insulin-like growth factor I/free prostate specific antigen (IGF-I/fPSA) ratio enhances prostate cancer detection in men with total PSA 4.0-10.0 ng/ml</title><title>Journal of surgical oncology</title><addtitle>J. Surg. Oncol</addtitle><description>Background Recent studies have suggested that IGF‐I and IGFBP‐3, in combination with PSA, may enhance PCa detection. This study was to investigate the use of serum IGF‐I and IGFBP‐3, and their combinations with prostate volume and fPSA in enhancing the discriminatory diagnosis of PCa in men with tPSA of 4.0–10.0 ng/ml. Methods Serum IGF‐I and IGFBP‐3 were determined by ELISA from 586 men with tPSA between 4.0 and 10.0 ng/ml. Of them, 281 were diagnosed with PCa and 305 without. ROC, univariate and multivariate logistic regression analyses were performed to evaluate the predictive performance of those parameters. Results IGF‐I, IGFD, IGF‐I/fPSA, and IGFBP‐3/fPSA were significantly higher in PCa cases than benign controls, whereas the differences of IGFBP‐3 and IGFBPD were statistically insignificant between the two groups, respectively. The AUC values indicated enhanced performance of IGF‐I/fPSA ratio (AUC = 0.753) in PCa detection compared with the currently used f/tPSA (AUC = 0.689). Multivariate logistic regression confirmed the observed relationships and identified IGF‐I/fPSA as independent factor in PCa presence. Conclusion Our data show that IGF‐I/fPSA as a promising marker can enhance PCa detection in ambiguous cases often found in the tPSA between 4.0 and 10.0 ng/ml. J. Surg. Oncol. 2007;96:54–61. © 2007 Wiley‐Liss, Inc.</description><subject>Aged</subject><subject>Biomarkers, Tumor - blood</subject><subject>Humans</subject><subject>insulin-like growth factor binding protein 3 (IGFBP-3)</subject><subject>Insulin-Like Growth Factor Binding Protein 3 - blood</subject><subject>insulin-like growth factor I (IGF-I)</subject><subject>Insulin-Like Growth Factor I - analysis</subject><subject>Logistic Models</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>prostate carcinoma (PCa)</subject><subject>prostate specific antigen (PSA)</subject><subject>Prostate-Specific Antigen - blood</subject><subject>Prostatic Neoplasms - diagnosis</subject><subject>ROC Curve</subject><subject>Sensitivity and Specificity</subject><issn>0022-4790</issn><issn>1096-9098</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc9uEzEQhy0EoqFw4AWQT4geNhnver32sSo0BFW0UkBIuVheZzZ1u39S26u079KHxSWBnrjYsvx9v_F4CHnPYMoA8tlNGKY5VJK_IBMGSmQKlHxJJukuz3il4Ii8CeEGAJQS_DU5YlXBy1IVE_K4RD921PVhbF2fte4W6cYPu3hNG2Pj4Oli1nhEuvVDiCYiDVu0rnGWmj66Dfb002J-niXqanl6Qr2JbqDYX5veYni27NPZ0zVGtInoU0XaJXnnUqU4RNPS5FM-hSx1BbTfzLr2LXnVmDbgu8N-TH6ef_lx9jW7uJwvzk4vMlsIxjNmjaplU6BUCpgpBAdcIxd1BbwqG8MxLRZ4ibWwkNfJkcraNTNNLqWwxTH5uM9Nz70bMUTduWCxbU2Pwxh0BUJyJlUCT_agTX0Fj43eetcZ_6AZ6KdR6DQK_WcUif1wCB3rDtfP5OHvEzDbAzvX4sP_k_S35eXfyGxvuBDx_p9h_K0WVVGV-tf3uV6t2Ge5XK30VfEb7KaiUg</recordid><startdate>20070701</startdate><enddate>20070701</enddate><creator>Zhigang, Zhao</creator><creator>Jieming, Liu</creator><creator>Su, Li</creator><creator>Wenlu, Shen</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><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>20070701</creationdate><title>Serum insulin-like growth factor I/free prostate specific antigen (IGF-I/fPSA) ratio enhances prostate cancer detection in men with total PSA 4.0-10.0 ng/ml</title><author>Zhigang, Zhao ; Jieming, Liu ; Su, Li ; Wenlu, Shen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3614-1ca9b8f3e89901a3640ede46b70475fa4e5fac045eb6c02b61489ccd1af2886c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Aged</topic><topic>Biomarkers, Tumor - blood</topic><topic>Humans</topic><topic>insulin-like growth factor binding protein 3 (IGFBP-3)</topic><topic>Insulin-Like Growth Factor Binding Protein 3 - blood</topic><topic>insulin-like growth factor I (IGF-I)</topic><topic>Insulin-Like Growth Factor I - analysis</topic><topic>Logistic Models</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Multivariate Analysis</topic><topic>prostate carcinoma (PCa)</topic><topic>prostate specific antigen (PSA)</topic><topic>Prostate-Specific Antigen - blood</topic><topic>Prostatic Neoplasms - diagnosis</topic><topic>ROC Curve</topic><topic>Sensitivity and Specificity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhigang, Zhao</creatorcontrib><creatorcontrib>Jieming, Liu</creatorcontrib><creatorcontrib>Su, Li</creatorcontrib><creatorcontrib>Wenlu, Shen</creatorcontrib><collection>Istex</collection><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>Journal of surgical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhigang, Zhao</au><au>Jieming, Liu</au><au>Su, Li</au><au>Wenlu, Shen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serum insulin-like growth factor I/free prostate specific antigen (IGF-I/fPSA) ratio enhances prostate cancer detection in men with total PSA 4.0-10.0 ng/ml</atitle><jtitle>Journal of surgical oncology</jtitle><addtitle>J. Surg. Oncol</addtitle><date>2007-07-01</date><risdate>2007</risdate><volume>96</volume><issue>1</issue><spage>54</spage><epage>61</epage><pages>54-61</pages><issn>0022-4790</issn><eissn>1096-9098</eissn><abstract>Background Recent studies have suggested that IGF‐I and IGFBP‐3, in combination with PSA, may enhance PCa detection. This study was to investigate the use of serum IGF‐I and IGFBP‐3, and their combinations with prostate volume and fPSA in enhancing the discriminatory diagnosis of PCa in men with tPSA of 4.0–10.0 ng/ml. Methods Serum IGF‐I and IGFBP‐3 were determined by ELISA from 586 men with tPSA between 4.0 and 10.0 ng/ml. Of them, 281 were diagnosed with PCa and 305 without. ROC, univariate and multivariate logistic regression analyses were performed to evaluate the predictive performance of those parameters. Results IGF‐I, IGFD, IGF‐I/fPSA, and IGFBP‐3/fPSA were significantly higher in PCa cases than benign controls, whereas the differences of IGFBP‐3 and IGFBPD were statistically insignificant between the two groups, respectively. The AUC values indicated enhanced performance of IGF‐I/fPSA ratio (AUC = 0.753) in PCa detection compared with the currently used f/tPSA (AUC = 0.689). Multivariate logistic regression confirmed the observed relationships and identified IGF‐I/fPSA as independent factor in PCa presence. Conclusion Our data show that IGF‐I/fPSA as a promising marker can enhance PCa detection in ambiguous cases often found in the tPSA between 4.0 and 10.0 ng/ml. J. Surg. Oncol. 2007;96:54–61. © 2007 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>17345593</pmid><doi>10.1002/jso.20784</doi><tpages>8</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0022-4790
ispartof Journal of surgical oncology, 2007-07, Vol.96 (1), p.54-61
issn 0022-4790
1096-9098
language eng
recordid cdi_proquest_miscellaneous_70684189
source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Aged
Biomarkers, Tumor - blood
Humans
insulin-like growth factor binding protein 3 (IGFBP-3)
Insulin-Like Growth Factor Binding Protein 3 - blood
insulin-like growth factor I (IGF-I)
Insulin-Like Growth Factor I - analysis
Logistic Models
Male
Middle Aged
Multivariate Analysis
prostate carcinoma (PCa)
prostate specific antigen (PSA)
Prostate-Specific Antigen - blood
Prostatic Neoplasms - diagnosis
ROC Curve
Sensitivity and Specificity
title Serum insulin-like growth factor I/free prostate specific antigen (IGF-I/fPSA) ratio enhances prostate cancer detection in men with total PSA 4.0-10.0 ng/ml
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-08T11%3A51%3A44IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Serum%20insulin-like%20growth%20factor%20I/free%20prostate%20specific%20antigen%20(IGF-I/fPSA)%20ratio%20enhances%20prostate%20cancer%20detection%20in%20men%20with%20total%20PSA%204.0-10.0%20ng/ml&rft.jtitle=Journal%20of%20surgical%20oncology&rft.au=Zhigang,%20Zhao&rft.date=2007-07-01&rft.volume=96&rft.issue=1&rft.spage=54&rft.epage=61&rft.pages=54-61&rft.issn=0022-4790&rft.eissn=1096-9098&rft_id=info:doi/10.1002/jso.20784&rft_dat=%3Cproquest_cross%3E70684189%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=70684189&rft_id=info:pmid/17345593&rfr_iscdi=true