Should AFP (or Any Biomarkers) Be Used for HCC Surveillance?
Purpose of Review The aim of this review is to address the controversy around the use of biomarkers for hepatocellular carcinoma (HCC) surveillance in individuals with cirrhosis or chronic hepatitis B who are at risk for development of liver cancer. Recent Findings Recent studies suggest that survei...
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Veröffentlicht in: | Current hepatology reports 2017-06, Vol.16 (2), p.137-145 |
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description | Purpose of Review
The aim of this review is to address the controversy around the use of biomarkers for hepatocellular carcinoma (HCC) surveillance in individuals with cirrhosis or chronic hepatitis B who are at risk for development of liver cancer.
Recent Findings
Recent studies suggest that surveillance for hepatocellular carcinoma is beneficial, even after adjustment for lead time and other biases. Alpha fetoprotein (AFP) is complementary to ultrasound (US) in surveillance, particularly in obese patients and patients with infiltrative tumors. US and AFP are both associated with harms to patients from false-positive overdiagnosis, with US appearing to cause greater harms. Including patient demographic characteristics and additional biomarkers into diagnostic models is beneficial. Recent studies emphasize the advantage of time trends in biomarkers over single cross-sectional measurements.
Summary
AFP and other biomarkers are complementary to US in surveillance for HCC, especially when applied in models including patient variables and incorporating time trends in biomarker levels. With advances in genetic and molecular analysis of tumors, we may be poised at the cusp of a revolution in HCC surveillance. |
doi_str_mv | 10.1007/s11901-017-0349-7 |
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The aim of this review is to address the controversy around the use of biomarkers for hepatocellular carcinoma (HCC) surveillance in individuals with cirrhosis or chronic hepatitis B who are at risk for development of liver cancer.
Recent Findings
Recent studies suggest that surveillance for hepatocellular carcinoma is beneficial, even after adjustment for lead time and other biases. Alpha fetoprotein (AFP) is complementary to ultrasound (US) in surveillance, particularly in obese patients and patients with infiltrative tumors. US and AFP are both associated with harms to patients from false-positive overdiagnosis, with US appearing to cause greater harms. Including patient demographic characteristics and additional biomarkers into diagnostic models is beneficial. Recent studies emphasize the advantage of time trends in biomarkers over single cross-sectional measurements.
Summary
AFP and other biomarkers are complementary to US in surveillance for HCC, especially when applied in models including patient variables and incorporating time trends in biomarker levels. With advances in genetic and molecular analysis of tumors, we may be poised at the cusp of a revolution in HCC surveillance.</description><identifier>ISSN: 2195-9595</identifier><identifier>EISSN: 2195-9595</identifier><identifier>DOI: 10.1007/s11901-017-0349-7</identifier><identifier>PMID: 29085770</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Hepatic Cancer (A Singal and A Mufti ; Hepatology ; Medicine ; Medicine & Public Health ; Section Editors ; Topical Collection on Hepatic Cancer</subject><ispartof>Current hepatology reports, 2017-06, Vol.16 (2), p.137-145</ispartof><rights>Springer Science+Business Media New York 2017</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2877-9c0f852efe40e8daa3da2988f6c4b0a185c0b9a7cacaf1261ced45ac8a269db83</citedby><cites>FETCH-LOGICAL-c2877-9c0f852efe40e8daa3da2988f6c4b0a185c0b9a7cacaf1261ced45ac8a269db83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11901-017-0349-7$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11901-017-0349-7$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,780,784,885,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29085770$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ahmed Mohammed, Hager F.</creatorcontrib><creatorcontrib>Roberts, Lewis R.</creatorcontrib><title>Should AFP (or Any Biomarkers) Be Used for HCC Surveillance?</title><title>Current hepatology reports</title><addtitle>Curr Hepatology Rep</addtitle><addtitle>Curr Hepatol Rep</addtitle><description>Purpose of Review
The aim of this review is to address the controversy around the use of biomarkers for hepatocellular carcinoma (HCC) surveillance in individuals with cirrhosis or chronic hepatitis B who are at risk for development of liver cancer.
Recent Findings
Recent studies suggest that surveillance for hepatocellular carcinoma is beneficial, even after adjustment for lead time and other biases. Alpha fetoprotein (AFP) is complementary to ultrasound (US) in surveillance, particularly in obese patients and patients with infiltrative tumors. US and AFP are both associated with harms to patients from false-positive overdiagnosis, with US appearing to cause greater harms. Including patient demographic characteristics and additional biomarkers into diagnostic models is beneficial. Recent studies emphasize the advantage of time trends in biomarkers over single cross-sectional measurements.
Summary
AFP and other biomarkers are complementary to US in surveillance for HCC, especially when applied in models including patient variables and incorporating time trends in biomarker levels. With advances in genetic and molecular analysis of tumors, we may be poised at the cusp of a revolution in HCC surveillance.</description><subject>Hepatic Cancer (A Singal and A Mufti</subject><subject>Hepatology</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Section Editors</subject><subject>Topical Collection on Hepatic Cancer</subject><issn>2195-9595</issn><issn>2195-9595</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp9kEFLAzEQhYMoKuoP8CJ7rIfVSbZpEhClXawVBAXtOaTZWd263dSkW-i_N6VV6sXTDLw3b2Y-Qs4pXFEAcR0oVUBToCKFrKtSsUeOGVU8VVzx_Z3-iJyFMAUAyrgQjB6SI6ZAxh6Oyc3rh2vrIukPX5KO80m_WSWDys2M_0QfLpMBJuOARVJGbZTnyWvrl1jVtWks3p2Sg9LUAc-29YSMh_dv-Sh9en54zPtPqWVSiFRZKCVnWGIXUBbGZIVhSsqyZ7sTMFRyCxNlhDXWlJT1qMWiy42VhvVUMZHZCbnd5M7byQwLi83Cm1rPfRXvXGlnKv1XaaoP_e6Wmve4YkBjQGcb4N1Xi2GhZ1WwuH4DXRt0RCV5prKMRyvdWK13IXgsf9dQ0GvwegNeR_B6DV6LOHOxe9_vxA_maGAbQ4hS845eT13rm8jsn9RvASCNPA</recordid><startdate>201706</startdate><enddate>201706</enddate><creator>Ahmed Mohammed, Hager F.</creator><creator>Roberts, Lewis R.</creator><general>Springer US</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201706</creationdate><title>Should AFP (or Any Biomarkers) Be Used for HCC Surveillance?</title><author>Ahmed Mohammed, Hager F. ; Roberts, Lewis R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2877-9c0f852efe40e8daa3da2988f6c4b0a185c0b9a7cacaf1261ced45ac8a269db83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Hepatic Cancer (A Singal and A Mufti</topic><topic>Hepatology</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Section Editors</topic><topic>Topical Collection on Hepatic Cancer</topic><toplevel>online_resources</toplevel><creatorcontrib>Ahmed Mohammed, Hager F.</creatorcontrib><creatorcontrib>Roberts, Lewis R.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Current hepatology reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ahmed Mohammed, Hager F.</au><au>Roberts, Lewis R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Should AFP (or Any Biomarkers) Be Used for HCC Surveillance?</atitle><jtitle>Current hepatology reports</jtitle><stitle>Curr Hepatology Rep</stitle><addtitle>Curr Hepatol Rep</addtitle><date>2017-06</date><risdate>2017</risdate><volume>16</volume><issue>2</issue><spage>137</spage><epage>145</epage><pages>137-145</pages><issn>2195-9595</issn><eissn>2195-9595</eissn><abstract>Purpose of Review
The aim of this review is to address the controversy around the use of biomarkers for hepatocellular carcinoma (HCC) surveillance in individuals with cirrhosis or chronic hepatitis B who are at risk for development of liver cancer.
Recent Findings
Recent studies suggest that surveillance for hepatocellular carcinoma is beneficial, even after adjustment for lead time and other biases. Alpha fetoprotein (AFP) is complementary to ultrasound (US) in surveillance, particularly in obese patients and patients with infiltrative tumors. US and AFP are both associated with harms to patients from false-positive overdiagnosis, with US appearing to cause greater harms. Including patient demographic characteristics and additional biomarkers into diagnostic models is beneficial. Recent studies emphasize the advantage of time trends in biomarkers over single cross-sectional measurements.
Summary
AFP and other biomarkers are complementary to US in surveillance for HCC, especially when applied in models including patient variables and incorporating time trends in biomarker levels. With advances in genetic and molecular analysis of tumors, we may be poised at the cusp of a revolution in HCC surveillance.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>29085770</pmid><doi>10.1007/s11901-017-0349-7</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Hepatic Cancer (A Singal and A Mufti Hepatology Medicine Medicine & Public Health Section Editors Topical Collection on Hepatic Cancer |
title | Should AFP (or Any Biomarkers) Be Used for HCC Surveillance? |
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