Performance of Protein Induced by Vitamin K Absence or Antagonist-II (PIVKA-II) for Hepatocellular Carcinoma Screening in Chinese Population
Alpha-fetoprotein (AFP) has long been used as an effective biomarker for hepatocellular carcinoma (HCC) screening; however, not all HCC patients can be detected with an elevated AFP level, especially in early HCC patients. Protein Induced by vitamin K absence or antagonist-II (PIVKA-II) is another s...
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description | Alpha-fetoprotein (AFP) has long been used as an effective biomarker for hepatocellular carcinoma (HCC) screening; however, not all HCC patients can be detected with an elevated AFP level, especially in early HCC patients. Protein Induced by vitamin K absence or antagonist-II (PIVKA-II) is another serum biomarker linked to HCC; however, sensitivity and specificity remain controversial and data in Chinese groups is even rarer.
To evaluate the performance of PIVKA-II alone and combined with AFP in HCC screening in Chinese population.
This retrospective study enrolled 150 HCC patients in Southwest Hospital, of which 16 patients were excluded due to lack of basic information. A total of 347 patients with hepatitis B, 105 with non-HCC cancers and 53 healthy people were enrolled as controls. Levels of AFP and PIVKA-II were measured by chemiluminescence enzyme immunoassay (CLEIA) and chemiluminescent microparticle Immunoassay (CMIA), respectively.
The sensitivity and specificity of PIVKA-II were 74.6% and 67.8% at a cutoff of 40 mAU/mL and 64.2% and 89.7% at a cutoff of 200 mAU/mL. The sensitivity and specificity of AFP were 76.7% and 65.0% at a cutoff of 20 ng/mL and 60.4% and 88.9% at a cutoff of 195.23 ng/mL. The combination of two markers had a sensitivity and specificity of 91.1% and 41.0%, respectively. The area under the receiving operating curve (AUROC) for PIVKA-II (0.756, 95% confidence interval, CI: 0.695 - 0.816) was less than the AUROC for AFP (0.823, 95% CI: 0.780 - 0.865), and in combination, the AUROC increased to 0.843 (95% CI: 0.801 - 0.885).
PIVKA-II was as efficient as AFP when used as a single marker for HCC screening and the combination of two biomarkers gave a better performance. |
doi_str_mv | 10.5812/hepatmon.28806v2 |
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To evaluate the performance of PIVKA-II alone and combined with AFP in HCC screening in Chinese population.
This retrospective study enrolled 150 HCC patients in Southwest Hospital, of which 16 patients were excluded due to lack of basic information. A total of 347 patients with hepatitis B, 105 with non-HCC cancers and 53 healthy people were enrolled as controls. Levels of AFP and PIVKA-II were measured by chemiluminescence enzyme immunoassay (CLEIA) and chemiluminescent microparticle Immunoassay (CMIA), respectively.
The sensitivity and specificity of PIVKA-II were 74.6% and 67.8% at a cutoff of 40 mAU/mL and 64.2% and 89.7% at a cutoff of 200 mAU/mL. The sensitivity and specificity of AFP were 76.7% and 65.0% at a cutoff of 20 ng/mL and 60.4% and 88.9% at a cutoff of 195.23 ng/mL. The combination of two markers had a sensitivity and specificity of 91.1% and 41.0%, respectively. The area under the receiving operating curve (AUROC) for PIVKA-II (0.756, 95% confidence interval, CI: 0.695 - 0.816) was less than the AUROC for AFP (0.823, 95% CI: 0.780 - 0.865), and in combination, the AUROC increased to 0.843 (95% CI: 0.801 - 0.885).
PIVKA-II was as efficient as AFP when used as a single marker for HCC screening and the combination of two biomarkers gave a better performance.</description><identifier>ISSN: 1735-143X</identifier><identifier>EISSN: 1735-3408</identifier><identifier>DOI: 10.5812/hepatmon.28806v2</identifier><identifier>PMID: 26300931</identifier><language>eng</language><publisher>Iran: Tehran Hepatitis Center</publisher><ispartof>Hepatitis monthly, 2015-07, Vol.15 (7), p.e28806-e28806</ispartof><rights>Copyright Tehran Hepatitis Center Jul 2015</rights><rights>Copyright © 2015, Kowsar Corp. 2015</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c424t-59a495a1174c97c3e952bbd507e3038be06c0f0ca6ba83150fcffbaae52bc7343</citedby><cites>FETCH-LOGICAL-c424t-59a495a1174c97c3e952bbd507e3038be06c0f0ca6ba83150fcffbaae52bc7343</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4539732/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4539732/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26300931$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yu, Rentao</creatorcontrib><creatorcontrib>Ding, Shitao</creatorcontrib><creatorcontrib>Tan, Wenting</creatorcontrib><creatorcontrib>Tan, Shun</creatorcontrib><creatorcontrib>Tan, Zhaoxia</creatorcontrib><creatorcontrib>Xiang, Shiqing</creatorcontrib><creatorcontrib>Zhou, Yi</creatorcontrib><creatorcontrib>Mao, Qing</creatorcontrib><creatorcontrib>Deng, Guohong</creatorcontrib><title>Performance of Protein Induced by Vitamin K Absence or Antagonist-II (PIVKA-II) for Hepatocellular Carcinoma Screening in Chinese Population</title><title>Hepatitis monthly</title><addtitle>Hepat Mon</addtitle><description>Alpha-fetoprotein (AFP) has long been used as an effective biomarker for hepatocellular carcinoma (HCC) screening; however, not all HCC patients can be detected with an elevated AFP level, especially in early HCC patients. Protein Induced by vitamin K absence or antagonist-II (PIVKA-II) is another serum biomarker linked to HCC; however, sensitivity and specificity remain controversial and data in Chinese groups is even rarer.
To evaluate the performance of PIVKA-II alone and combined with AFP in HCC screening in Chinese population.
This retrospective study enrolled 150 HCC patients in Southwest Hospital, of which 16 patients were excluded due to lack of basic information. A total of 347 patients with hepatitis B, 105 with non-HCC cancers and 53 healthy people were enrolled as controls. Levels of AFP and PIVKA-II were measured by chemiluminescence enzyme immunoassay (CLEIA) and chemiluminescent microparticle Immunoassay (CMIA), respectively.
The sensitivity and specificity of PIVKA-II were 74.6% and 67.8% at a cutoff of 40 mAU/mL and 64.2% and 89.7% at a cutoff of 200 mAU/mL. The sensitivity and specificity of AFP were 76.7% and 65.0% at a cutoff of 20 ng/mL and 60.4% and 88.9% at a cutoff of 195.23 ng/mL. The combination of two markers had a sensitivity and specificity of 91.1% and 41.0%, respectively. The area under the receiving operating curve (AUROC) for PIVKA-II (0.756, 95% confidence interval, CI: 0.695 - 0.816) was less than the AUROC for AFP (0.823, 95% CI: 0.780 - 0.865), and in combination, the AUROC increased to 0.843 (95% CI: 0.801 - 0.885).
PIVKA-II was as efficient as AFP when used as a single marker for HCC screening and the combination of two biomarkers gave a better performance.</description><issn>1735-143X</issn><issn>1735-3408</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkU9v1DAQxS0Eon_gzglZ4tIeUsZ2HCcXpNUKaNRKrARU3CzHO9l1ldiLnVTqd-BD46XbCjjNaOY3T_P0CHnD4ELWjL_f4s5MY_AXvK6huuPPyDFTQhaihPr5oWel-HFETlK6BZA1KP6SHPFKADSCHZNfK4x9iKPxFmno6SqGCZ2nrV_PFte0u6c3bjJjHl3RRZfwDxfpwk9mE7xLU9G29GzV3lwtcndOsxi93L8VLA7DPJhIlyZa58No6FcbEb3zG5r1llvnMSFdhV3GJhf8K_KiN0PC14d6Sr5_-vhteVlcf_ncLhfXhS15ORWyMWUjDWOqtI2yAhvJu24tQaEAUXcIlYUerKk6Uwsmobd93xmDGbNKlOKUfHjQ3c3diGuLfopm0LvoRhPvdTBO_7vxbqs34U6XUjRK8CxwdhCI4eeMadKjS3u_xmOYk2YKKqkqYDKj7_5Db8Mcfba3p1StgJcqU_BA2RhSitg_PcNA76PWj1HrQ9T55O3fJp4OHrMVvwEgw6jL</recordid><startdate>20150701</startdate><enddate>20150701</enddate><creator>Yu, Rentao</creator><creator>Ding, Shitao</creator><creator>Tan, Wenting</creator><creator>Tan, Shun</creator><creator>Tan, Zhaoxia</creator><creator>Xiang, Shiqing</creator><creator>Zhou, Yi</creator><creator>Mao, Qing</creator><creator>Deng, Guohong</creator><general>Tehran Hepatitis Center</general><general>Kowsar</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>CWDGH</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20150701</creationdate><title>Performance of Protein Induced by Vitamin K Absence or Antagonist-II (PIVKA-II) for Hepatocellular Carcinoma Screening in Chinese Population</title><author>Yu, Rentao ; Ding, Shitao ; Tan, Wenting ; Tan, Shun ; Tan, Zhaoxia ; Xiang, Shiqing ; Zhou, Yi ; Mao, Qing ; Deng, Guohong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c424t-59a495a1174c97c3e952bbd507e3038be06c0f0ca6ba83150fcffbaae52bc7343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Yu, Rentao</creatorcontrib><creatorcontrib>Ding, Shitao</creatorcontrib><creatorcontrib>Tan, Wenting</creatorcontrib><creatorcontrib>Tan, Shun</creatorcontrib><creatorcontrib>Tan, Zhaoxia</creatorcontrib><creatorcontrib>Xiang, Shiqing</creatorcontrib><creatorcontrib>Zhou, Yi</creatorcontrib><creatorcontrib>Mao, Qing</creatorcontrib><creatorcontrib>Deng, Guohong</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Middle East & Africa Database</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Hepatitis monthly</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yu, Rentao</au><au>Ding, Shitao</au><au>Tan, Wenting</au><au>Tan, Shun</au><au>Tan, Zhaoxia</au><au>Xiang, Shiqing</au><au>Zhou, Yi</au><au>Mao, Qing</au><au>Deng, Guohong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Performance of Protein Induced by Vitamin K Absence or Antagonist-II (PIVKA-II) for Hepatocellular Carcinoma Screening in Chinese Population</atitle><jtitle>Hepatitis monthly</jtitle><addtitle>Hepat Mon</addtitle><date>2015-07-01</date><risdate>2015</risdate><volume>15</volume><issue>7</issue><spage>e28806</spage><epage>e28806</epage><pages>e28806-e28806</pages><issn>1735-143X</issn><eissn>1735-3408</eissn><abstract>Alpha-fetoprotein (AFP) has long been used as an effective biomarker for hepatocellular carcinoma (HCC) screening; however, not all HCC patients can be detected with an elevated AFP level, especially in early HCC patients. Protein Induced by vitamin K absence or antagonist-II (PIVKA-II) is another serum biomarker linked to HCC; however, sensitivity and specificity remain controversial and data in Chinese groups is even rarer.
To evaluate the performance of PIVKA-II alone and combined with AFP in HCC screening in Chinese population.
This retrospective study enrolled 150 HCC patients in Southwest Hospital, of which 16 patients were excluded due to lack of basic information. A total of 347 patients with hepatitis B, 105 with non-HCC cancers and 53 healthy people were enrolled as controls. Levels of AFP and PIVKA-II were measured by chemiluminescence enzyme immunoassay (CLEIA) and chemiluminescent microparticle Immunoassay (CMIA), respectively.
The sensitivity and specificity of PIVKA-II were 74.6% and 67.8% at a cutoff of 40 mAU/mL and 64.2% and 89.7% at a cutoff of 200 mAU/mL. The sensitivity and specificity of AFP were 76.7% and 65.0% at a cutoff of 20 ng/mL and 60.4% and 88.9% at a cutoff of 195.23 ng/mL. The combination of two markers had a sensitivity and specificity of 91.1% and 41.0%, respectively. The area under the receiving operating curve (AUROC) for PIVKA-II (0.756, 95% confidence interval, CI: 0.695 - 0.816) was less than the AUROC for AFP (0.823, 95% CI: 0.780 - 0.865), and in combination, the AUROC increased to 0.843 (95% CI: 0.801 - 0.885).
PIVKA-II was as efficient as AFP when used as a single marker for HCC screening and the combination of two biomarkers gave a better performance.</abstract><cop>Iran</cop><pub>Tehran Hepatitis Center</pub><pmid>26300931</pmid><doi>10.5812/hepatmon.28806v2</doi><oa>free_for_read</oa></addata></record> |
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title | Performance of Protein Induced by Vitamin K Absence or Antagonist-II (PIVKA-II) for Hepatocellular Carcinoma Screening in Chinese Population |
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