High serum interleukin‐6 level predicts future hepatocellular carcinoma development in patients with chronic hepatitis B
Increased interleukin‐6 (IL‐6) production is implicated in the pathogenesis of hepatocellular carcinoma (HCC) in animal models. Although previous studies showed that HCC patients had higher serum IL‐6 level at the time of diagnosis, it is unclear if the cytokine contributes to the development of HCC...
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creator | Wong, Vincent Wai‐Sun Yu, Jun Cheng, Alfred Sze‐Lok Wong, Grace Lai‐Hung Chan, Hoi‐Yun Chu, Eagle Siu‐Hong Ng, Enders Kai‐On Chan, Francis Ka‐Leung Sung, Joseph Jao‐Yao Chan, Henry Lik‐Yuen |
description | Increased interleukin‐6 (IL‐6) production is implicated in the pathogenesis of hepatocellular carcinoma (HCC) in animal models. Although previous studies showed that HCC patients had higher serum IL‐6 level at the time of diagnosis, it is unclear if the cytokine contributes to the development of HCC or is just a reaction to cancer. To address this question, we performed a nested case‐control study. Consecutive chronic hepatitis B patients were recruited from 1997 to 2000 and followed till 2008. Profiling of 27 cytokines, chemokines and growth factors was performed at baseline, date of peak alanine aminotransferase (ALT) level and the last visit. Thirty‐seven patients developed HCC at a median follow‐up of 62 months (interquartile range: 41–110). Serum IL‐6 was higher in patients with HCC than controls both during peak ALT and at the last visit (both p = 0.02). Patients with IL‐6 above 7 pg/ml during peak ALT had increased risk of HCC or death (adjusted hazard ratio 3.0; 95% confidence interval 1.2, 7.8; p = 0.02). The sensitivity, specificity, positive and negative predictive values of this cutoff to predict future HCC development were 70%, 73%, 72% and 71%, respectively. Combination of IL‐6 and AFP improved the sensitivity in diagnosing HCC or predicting future HCC development. In conclusion, high serum IL‐6 level predates the development of HCC in chronic hepatitis B patients, and has moderate accuracy in predicting future cancer. This may assist clinicians in selecting high‐risk patients for HCC surveillance program. © 2009 UICC |
doi_str_mv | 10.1002/ijc.24281 |
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Although previous studies showed that HCC patients had higher serum IL‐6 level at the time of diagnosis, it is unclear if the cytokine contributes to the development of HCC or is just a reaction to cancer. To address this question, we performed a nested case‐control study. Consecutive chronic hepatitis B patients were recruited from 1997 to 2000 and followed till 2008. Profiling of 27 cytokines, chemokines and growth factors was performed at baseline, date of peak alanine aminotransferase (ALT) level and the last visit. Thirty‐seven patients developed HCC at a median follow‐up of 62 months (interquartile range: 41–110). Serum IL‐6 was higher in patients with HCC than controls both during peak ALT and at the last visit (both p = 0.02). Patients with IL‐6 above 7 pg/ml during peak ALT had increased risk of HCC or death (adjusted hazard ratio 3.0; 95% confidence interval 1.2, 7.8; p = 0.02). The sensitivity, specificity, positive and negative predictive values of this cutoff to predict future HCC development were 70%, 73%, 72% and 71%, respectively. Combination of IL‐6 and AFP improved the sensitivity in diagnosing HCC or predicting future HCC development. In conclusion, high serum IL‐6 level predates the development of HCC in chronic hepatitis B patients, and has moderate accuracy in predicting future cancer. This may assist clinicians in selecting high‐risk patients for HCC surveillance program. © 2009 UICC</description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/ijc.24281</identifier><identifier>PMID: 19267406</identifier><identifier>CODEN: IJCNAW</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Biological and medical sciences ; Biomarkers, Tumor - blood ; Carcinoma, Hepatocellular - blood ; Carcinoma, Hepatocellular - virology ; Case-Control Studies ; cytokines ; False Positive Reactions ; Female ; fibrosis ; Gastroenterology. Liver. Pancreas. Abdomen ; hepatitis B ; Hepatitis B virus - isolation & purification ; Hepatitis B, Chronic - blood ; Hepatitis B, Chronic - virology ; Humans ; Interleukin-6 - blood ; interleukin‐6 ; liver neoplasms ; Liver Neoplasms - blood ; Liver Neoplasms - virology ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Male ; Medical sciences ; Middle Aged ; Neoplasm Staging ; Predictive Value of Tests ; Prognosis ; Risk Factors ; Sensitivity and Specificity ; Tumors</subject><ispartof>International journal of cancer, 2009-06, Vol.124 (12), p.2766-2770</ispartof><rights>Copyright © 2009 UICC</rights><rights>2009 INIST-CNRS</rights><rights>Copyright 2008 UICC.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4191-8c60523717e1c8cc3c6e49278df14271389028aef52becb9d8af34f34760d8ea3</citedby><cites>FETCH-LOGICAL-c4191-8c60523717e1c8cc3c6e49278df14271389028aef52becb9d8af34f34760d8ea3</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%2Fijc.24281$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fijc.24281$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21370907$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19267406$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wong, Vincent Wai‐Sun</creatorcontrib><creatorcontrib>Yu, Jun</creatorcontrib><creatorcontrib>Cheng, Alfred Sze‐Lok</creatorcontrib><creatorcontrib>Wong, Grace Lai‐Hung</creatorcontrib><creatorcontrib>Chan, Hoi‐Yun</creatorcontrib><creatorcontrib>Chu, Eagle Siu‐Hong</creatorcontrib><creatorcontrib>Ng, Enders Kai‐On</creatorcontrib><creatorcontrib>Chan, Francis Ka‐Leung</creatorcontrib><creatorcontrib>Sung, Joseph Jao‐Yao</creatorcontrib><creatorcontrib>Chan, Henry Lik‐Yuen</creatorcontrib><title>High serum interleukin‐6 level predicts future hepatocellular carcinoma development in patients with chronic hepatitis B</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><description>Increased interleukin‐6 (IL‐6) production is implicated in the pathogenesis of hepatocellular carcinoma (HCC) in animal models. Although previous studies showed that HCC patients had higher serum IL‐6 level at the time of diagnosis, it is unclear if the cytokine contributes to the development of HCC or is just a reaction to cancer. To address this question, we performed a nested case‐control study. Consecutive chronic hepatitis B patients were recruited from 1997 to 2000 and followed till 2008. Profiling of 27 cytokines, chemokines and growth factors was performed at baseline, date of peak alanine aminotransferase (ALT) level and the last visit. Thirty‐seven patients developed HCC at a median follow‐up of 62 months (interquartile range: 41–110). Serum IL‐6 was higher in patients with HCC than controls both during peak ALT and at the last visit (both p = 0.02). Patients with IL‐6 above 7 pg/ml during peak ALT had increased risk of HCC or death (adjusted hazard ratio 3.0; 95% confidence interval 1.2, 7.8; p = 0.02). The sensitivity, specificity, positive and negative predictive values of this cutoff to predict future HCC development were 70%, 73%, 72% and 71%, respectively. Combination of IL‐6 and AFP improved the sensitivity in diagnosing HCC or predicting future HCC development. In conclusion, high serum IL‐6 level predates the development of HCC in chronic hepatitis B patients, and has moderate accuracy in predicting future cancer. This may assist clinicians in selecting high‐risk patients for HCC surveillance program. © 2009 UICC</description><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor - blood</subject><subject>Carcinoma, Hepatocellular - blood</subject><subject>Carcinoma, Hepatocellular - virology</subject><subject>Case-Control Studies</subject><subject>cytokines</subject><subject>False Positive Reactions</subject><subject>Female</subject><subject>fibrosis</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>hepatitis B</subject><subject>Hepatitis B virus - isolation & purification</subject><subject>Hepatitis B, Chronic - blood</subject><subject>Hepatitis B, Chronic - virology</subject><subject>Humans</subject><subject>Interleukin-6 - blood</subject><subject>interleukin‐6</subject><subject>liver neoplasms</subject><subject>Liver Neoplasms - blood</subject><subject>Liver Neoplasms - virology</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neoplasm Staging</subject><subject>Predictive Value of Tests</subject><subject>Prognosis</subject><subject>Risk Factors</subject><subject>Sensitivity and Specificity</subject><subject>Tumors</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0c1u1DAQB3ALUdGlcOAFkC8gcUg742Tt5EhXhbaqxAXOkXcyYV2cD-yEqj3xCDwjT4KXrOCEkCzZkn_-j-0R4gXCKQKoM3dLp6pQJT4SK4TKZKBw_Vis0h5kBnN9LJ7GeAuAuIbiiTjGSmlTgF6Jh0v3eScjh7mTrp84eJ6_uP7n9x9aev7GXo6BG0dTlO08zYHljkc7DcTez94GSTaQ64fOymbPh7HjfkpRMimXllHeuWknaReG3tFy2k0uyvNn4qi1PvLzw3wiPr27-Li5zG4-vL_avL3JqMAKs5I0rFVu0DBSSZST5qJSpmxaLFR6XVmBKi23a7Vl2lZNadu8SMNoaEq2-Yl4veSOYfg6c5zqzsX9_W3PwxxrnTKK9C__hQp0rlCpBN8skMIQY-C2HoPrbLivEep9R-rUkfp3R5J9eQidtx03f-WhBQm8OgAbyfo22J5c_OMU5gYqMMmdLe7Oeb7_d8X66nqzlP4FWeikjg</recordid><startdate>20090615</startdate><enddate>20090615</enddate><creator>Wong, Vincent Wai‐Sun</creator><creator>Yu, Jun</creator><creator>Cheng, Alfred Sze‐Lok</creator><creator>Wong, Grace Lai‐Hung</creator><creator>Chan, Hoi‐Yun</creator><creator>Chu, Eagle Siu‐Hong</creator><creator>Ng, Enders Kai‐On</creator><creator>Chan, Francis Ka‐Leung</creator><creator>Sung, Joseph Jao‐Yao</creator><creator>Chan, Henry Lik‐Yuen</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Blackwell</general><scope>IQODW</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>7T5</scope><scope>7U7</scope><scope>7U9</scope><scope>C1K</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20090615</creationdate><title>High serum interleukin‐6 level predicts future hepatocellular carcinoma development in patients with chronic hepatitis B</title><author>Wong, Vincent Wai‐Sun ; Yu, Jun ; Cheng, Alfred Sze‐Lok ; Wong, Grace Lai‐Hung ; Chan, Hoi‐Yun ; Chu, Eagle Siu‐Hong ; Ng, Enders Kai‐On ; Chan, Francis Ka‐Leung ; Sung, Joseph Jao‐Yao ; Chan, Henry Lik‐Yuen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4191-8c60523717e1c8cc3c6e49278df14271389028aef52becb9d8af34f34760d8ea3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor - blood</topic><topic>Carcinoma, Hepatocellular - blood</topic><topic>Carcinoma, Hepatocellular - virology</topic><topic>Case-Control Studies</topic><topic>cytokines</topic><topic>False Positive Reactions</topic><topic>Female</topic><topic>fibrosis</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>hepatitis B</topic><topic>Hepatitis B virus - isolation & purification</topic><topic>Hepatitis B, Chronic - blood</topic><topic>Hepatitis B, Chronic - virology</topic><topic>Humans</topic><topic>Interleukin-6 - blood</topic><topic>interleukin‐6</topic><topic>liver neoplasms</topic><topic>Liver Neoplasms - blood</topic><topic>Liver Neoplasms - virology</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neoplasm Staging</topic><topic>Predictive Value of Tests</topic><topic>Prognosis</topic><topic>Risk Factors</topic><topic>Sensitivity and Specificity</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wong, Vincent Wai‐Sun</creatorcontrib><creatorcontrib>Yu, Jun</creatorcontrib><creatorcontrib>Cheng, Alfred Sze‐Lok</creatorcontrib><creatorcontrib>Wong, Grace Lai‐Hung</creatorcontrib><creatorcontrib>Chan, Hoi‐Yun</creatorcontrib><creatorcontrib>Chu, Eagle Siu‐Hong</creatorcontrib><creatorcontrib>Ng, Enders Kai‐On</creatorcontrib><creatorcontrib>Chan, Francis Ka‐Leung</creatorcontrib><creatorcontrib>Sung, Joseph Jao‐Yao</creatorcontrib><creatorcontrib>Chan, Henry Lik‐Yuen</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wong, Vincent Wai‐Sun</au><au>Yu, Jun</au><au>Cheng, Alfred Sze‐Lok</au><au>Wong, Grace Lai‐Hung</au><au>Chan, Hoi‐Yun</au><au>Chu, Eagle Siu‐Hong</au><au>Ng, Enders Kai‐On</au><au>Chan, Francis Ka‐Leung</au><au>Sung, Joseph Jao‐Yao</au><au>Chan, Henry Lik‐Yuen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High serum interleukin‐6 level predicts future hepatocellular carcinoma development in patients with chronic hepatitis B</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>2009-06-15</date><risdate>2009</risdate><volume>124</volume><issue>12</issue><spage>2766</spage><epage>2770</epage><pages>2766-2770</pages><issn>0020-7136</issn><eissn>1097-0215</eissn><coden>IJCNAW</coden><abstract>Increased interleukin‐6 (IL‐6) production is implicated in the pathogenesis of hepatocellular carcinoma (HCC) in animal models. Although previous studies showed that HCC patients had higher serum IL‐6 level at the time of diagnosis, it is unclear if the cytokine contributes to the development of HCC or is just a reaction to cancer. To address this question, we performed a nested case‐control study. Consecutive chronic hepatitis B patients were recruited from 1997 to 2000 and followed till 2008. Profiling of 27 cytokines, chemokines and growth factors was performed at baseline, date of peak alanine aminotransferase (ALT) level and the last visit. Thirty‐seven patients developed HCC at a median follow‐up of 62 months (interquartile range: 41–110). Serum IL‐6 was higher in patients with HCC than controls both during peak ALT and at the last visit (both p = 0.02). Patients with IL‐6 above 7 pg/ml during peak ALT had increased risk of HCC or death (adjusted hazard ratio 3.0; 95% confidence interval 1.2, 7.8; p = 0.02). The sensitivity, specificity, positive and negative predictive values of this cutoff to predict future HCC development were 70%, 73%, 72% and 71%, respectively. Combination of IL‐6 and AFP improved the sensitivity in diagnosing HCC or predicting future HCC development. In conclusion, high serum IL‐6 level predates the development of HCC in chronic hepatitis B patients, and has moderate accuracy in predicting future cancer. This may assist clinicians in selecting high‐risk patients for HCC surveillance program. © 2009 UICC</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>19267406</pmid><doi>10.1002/ijc.24281</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biological and medical sciences Biomarkers, Tumor - blood Carcinoma, Hepatocellular - blood Carcinoma, Hepatocellular - virology Case-Control Studies cytokines False Positive Reactions Female fibrosis Gastroenterology. Liver. Pancreas. Abdomen hepatitis B Hepatitis B virus - isolation & purification Hepatitis B, Chronic - blood Hepatitis B, Chronic - virology Humans Interleukin-6 - blood interleukin‐6 liver neoplasms Liver Neoplasms - blood Liver Neoplasms - virology Liver. Biliary tract. Portal circulation. Exocrine pancreas Male Medical sciences Middle Aged Neoplasm Staging Predictive Value of Tests Prognosis Risk Factors Sensitivity and Specificity Tumors |
title | High serum interleukin‐6 level predicts future hepatocellular carcinoma development in patients with chronic hepatitis B |
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