Liver transplantation for hepatocellular cancer: UCL experience in 137 adult cirrhotic patients. Alpha-foetoprotein level and locoregional treatment as refined selection criteria

Summary Liver transplantation (LT) is a validated treatment for selected cirrhotics with hepatocellular cancer (HCC). A retrospective single center study including 137 recipients having proven HCC was done to refine inclusion criteria for LT as well as to look at impact of locoregional treatment (LR...

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Veröffentlicht in:Transplant international 2012-08, Vol.25 (8), p.867-875
Hauptverfasser: Ciccarelli, Olga, Lai, Quirino, Goffette, Pierre, Finet, Patrice, De Reyck, Chantal, Roggen, Francine, Sempoux, Christine, Doffagne, Erik, Reding, Raymond, Lerut, Jan
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container_end_page 875
container_issue 8
container_start_page 867
container_title Transplant international
container_volume 25
creator Ciccarelli, Olga
Lai, Quirino
Goffette, Pierre
Finet, Patrice
De Reyck, Chantal
Roggen, Francine
Sempoux, Christine
Doffagne, Erik
Reding, Raymond
Lerut, Jan
description Summary Liver transplantation (LT) is a validated treatment for selected cirrhotics with hepatocellular cancer (HCC). A retrospective single center study including 137 recipients having proven HCC was done to refine inclusion criteria for LT as well as to look at impact of locoregional treatment (LRT) on outcome. At pre‐LT imaging, 42 (30.6%) patients were Milan criteria (MC)‐OUT; 28 (20.4%) were University of California San Francisco criteria (UCSFC)‐OUT. Pre‐LT LRT was performed in 109 (79.6%) patients. Multivariate analysis identified four factors to be independently predictive of recurrence: tumour number >3, AFP level ≥400 ng/ml, microvascular invasion and rejection needing anti‐lymphocytic antibodies. When considering pre‐transplant variables only, AFP level ≥400 ng/ml (HR = 5.13; P 
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Alpha-foetoprotein level and locoregional treatment as refined selection criteria</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>Ciccarelli, Olga ; Lai, Quirino ; Goffette, Pierre ; Finet, Patrice ; De Reyck, Chantal ; Roggen, Francine ; Sempoux, Christine ; Doffagne, Erik ; Reding, Raymond ; Lerut, Jan</creator><creatorcontrib>Ciccarelli, Olga ; Lai, Quirino ; Goffette, Pierre ; Finet, Patrice ; De Reyck, Chantal ; Roggen, Francine ; Sempoux, Christine ; Doffagne, Erik ; Reding, Raymond ; Lerut, Jan</creatorcontrib><description>Summary Liver transplantation (LT) is a validated treatment for selected cirrhotics with hepatocellular cancer (HCC). A retrospective single center study including 137 recipients having proven HCC was done to refine inclusion criteria for LT as well as to look at impact of locoregional treatment (LRT) on outcome. At pre‐LT imaging, 42 (30.6%) patients were Milan criteria (MC)‐OUT; 28 (20.4%) were University of California San Francisco criteria (UCSFC)‐OUT. Pre‐LT LRT was performed in 109 (79.6%) patients. Multivariate analysis identified four factors to be independently predictive of recurrence: tumour number &gt;3, AFP level ≥400 ng/ml, microvascular invasion and rejection needing anti‐lymphocytic antibodies. When considering pre‐transplant variables only, AFP level ≥400 ng/ml (HR = 5.13; P &lt; 0.0001) was the unique risk factor for recurrence; conversely, application of LRT was protective (HR = 0.42; P = 0.04). MC‐IN patients having LRT (n = 79) had the best 5‐year tumour‐free survival (TFS) (91.6%). MC‐IN patients without LRT (n = 16) and MC‐OUT patients with LRT (n = 30) had similar good TFS (72.7% vs.77.5%); finally MC‐OUT patients without LRT (n = 12) had the worst results (45.0%; vs. 1st group: P &lt; 0.0001). Immediate pre‐LT AFP and aggressive pre‐transplant LRT strategy, especially in MC‐OUT patients, are both important elements to further expand inclusion criteria without compromising long‐term results of HCC liver recipients.</description><identifier>ISSN: 0934-0874</identifier><identifier>EISSN: 1432-2277</identifier><identifier>DOI: 10.1111/j.1432-2277.2012.01512.x</identifier><identifier>PMID: 22716073</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adult ; Aged ; alpha-Fetoproteins - metabolism ; alpha-foetoprotein ; Combined Modality Therapy ; downstaging ; Female ; hepatocellular cancer ; Humans ; Liver cancer ; Liver cirrhosis ; Liver Cirrhosis - complications ; Liver Neoplasms - etiology ; Liver Neoplasms - surgery ; Liver Neoplasms - therapy ; liver transplantation ; Liver Transplantation - mortality ; locoregional treatment ; Male ; Middle Aged ; Multivariate analysis ; Patient Selection ; Pulsed Radiofrequency Treatment ; Retrospective Studies ; Transplants &amp; implants</subject><ispartof>Transplant international, 2012-08, Vol.25 (8), p.867-875</ispartof><rights>2012 The Authors. Transplant International © 2012 European Society for Organ Transplantation</rights><rights>2012 The Authors. Transplant International © 2012 European Society for Organ Transplantation.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4522-76f3dbef0c0d1c71bcc26d902ee185c038dbc4121d66de70f609a0e097253923</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1432-2277.2012.01512.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1432-2277.2012.01512.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,778,782,1414,27911,27912,45561,45562</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22716073$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ciccarelli, Olga</creatorcontrib><creatorcontrib>Lai, Quirino</creatorcontrib><creatorcontrib>Goffette, Pierre</creatorcontrib><creatorcontrib>Finet, Patrice</creatorcontrib><creatorcontrib>De Reyck, Chantal</creatorcontrib><creatorcontrib>Roggen, Francine</creatorcontrib><creatorcontrib>Sempoux, Christine</creatorcontrib><creatorcontrib>Doffagne, Erik</creatorcontrib><creatorcontrib>Reding, Raymond</creatorcontrib><creatorcontrib>Lerut, Jan</creatorcontrib><title>Liver transplantation for hepatocellular cancer: UCL experience in 137 adult cirrhotic patients. Alpha-foetoprotein level and locoregional treatment as refined selection criteria</title><title>Transplant international</title><addtitle>Transpl Int</addtitle><description>Summary Liver transplantation (LT) is a validated treatment for selected cirrhotics with hepatocellular cancer (HCC). A retrospective single center study including 137 recipients having proven HCC was done to refine inclusion criteria for LT as well as to look at impact of locoregional treatment (LRT) on outcome. At pre‐LT imaging, 42 (30.6%) patients were Milan criteria (MC)‐OUT; 28 (20.4%) were University of California San Francisco criteria (UCSFC)‐OUT. Pre‐LT LRT was performed in 109 (79.6%) patients. Multivariate analysis identified four factors to be independently predictive of recurrence: tumour number &gt;3, AFP level ≥400 ng/ml, microvascular invasion and rejection needing anti‐lymphocytic antibodies. When considering pre‐transplant variables only, AFP level ≥400 ng/ml (HR = 5.13; P &lt; 0.0001) was the unique risk factor for recurrence; conversely, application of LRT was protective (HR = 0.42; P = 0.04). MC‐IN patients having LRT (n = 79) had the best 5‐year tumour‐free survival (TFS) (91.6%). MC‐IN patients without LRT (n = 16) and MC‐OUT patients with LRT (n = 30) had similar good TFS (72.7% vs.77.5%); finally MC‐OUT patients without LRT (n = 12) had the worst results (45.0%; vs. 1st group: P &lt; 0.0001). Immediate pre‐LT AFP and aggressive pre‐transplant LRT strategy, especially in MC‐OUT patients, are both important elements to further expand inclusion criteria without compromising long‐term results of HCC liver recipients.</description><subject>Adult</subject><subject>Aged</subject><subject>alpha-Fetoproteins - metabolism</subject><subject>alpha-foetoprotein</subject><subject>Combined Modality Therapy</subject><subject>downstaging</subject><subject>Female</subject><subject>hepatocellular cancer</subject><subject>Humans</subject><subject>Liver cancer</subject><subject>Liver cirrhosis</subject><subject>Liver Cirrhosis - complications</subject><subject>Liver Neoplasms - etiology</subject><subject>Liver Neoplasms - surgery</subject><subject>Liver Neoplasms - therapy</subject><subject>liver transplantation</subject><subject>Liver Transplantation - mortality</subject><subject>locoregional treatment</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Multivariate analysis</subject><subject>Patient Selection</subject><subject>Pulsed Radiofrequency Treatment</subject><subject>Retrospective Studies</subject><subject>Transplants &amp; implants</subject><issn>0934-0874</issn><issn>1432-2277</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkd9u0zAUxiMEYmXwCsgSN9wkHDuJ3SBxMVXbmBaBhIq4tFznhLq4cbCd0b0WT4izbr3Akv8o3-_zOc6XZYRCQdP4sCtoVbKcMSEKBpQVQOu0Hp5li5PwPFtAU1Y5LEV1lr0KYQcAbFnDy-ws6ZSDKBfZ39bcoSfRqyGMVg1RReMG0jtPtjiq6DRaO1nliVaDRv-RfF-1BA8jeoPpAzEDoaUgqptsJNp4v3XRaJKsSY-hIBd23Kq8dxjd6F3EZLB4h5aooSPWaefxZyqpbGoCVdwnF1GBeOzNgB0JaFE_9KS9iamqep296JUN-OZxP8_WV5fr1ee8_Xp9s7poc13VjOWC92W3wR40dFQLutGa8a4BhkiXtYZy2W10RRntOO9QQM-hUYDQCFaXDSvPs_fHa1PXvycMUe5NmP-GGtBNQVJgFa9qCjyh7_5Dd27y6UmJEpw3qRaDRL19pKbNHjs5erNX_l4-hZGAT0fgj7F4f9IpyDl0uZNztjMu5By6fAhdHuT62818Sv786Dch4uHkV_6X5KIUtfzx5TrNdlWLq7W8Lf8Bnwqx2w</recordid><startdate>201208</startdate><enddate>201208</enddate><creator>Ciccarelli, Olga</creator><creator>Lai, Quirino</creator><creator>Goffette, Pierre</creator><creator>Finet, Patrice</creator><creator>De Reyck, Chantal</creator><creator>Roggen, Francine</creator><creator>Sempoux, Christine</creator><creator>Doffagne, Erik</creator><creator>Reding, Raymond</creator><creator>Lerut, Jan</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QO</scope><scope>7T5</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201208</creationdate><title>Liver transplantation for hepatocellular cancer: UCL experience in 137 adult cirrhotic patients. 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Alpha-foetoprotein level and locoregional treatment as refined selection criteria</atitle><jtitle>Transplant international</jtitle><addtitle>Transpl Int</addtitle><date>2012-08</date><risdate>2012</risdate><volume>25</volume><issue>8</issue><spage>867</spage><epage>875</epage><pages>867-875</pages><issn>0934-0874</issn><eissn>1432-2277</eissn><abstract>Summary Liver transplantation (LT) is a validated treatment for selected cirrhotics with hepatocellular cancer (HCC). A retrospective single center study including 137 recipients having proven HCC was done to refine inclusion criteria for LT as well as to look at impact of locoregional treatment (LRT) on outcome. At pre‐LT imaging, 42 (30.6%) patients were Milan criteria (MC)‐OUT; 28 (20.4%) were University of California San Francisco criteria (UCSFC)‐OUT. Pre‐LT LRT was performed in 109 (79.6%) patients. Multivariate analysis identified four factors to be independently predictive of recurrence: tumour number &gt;3, AFP level ≥400 ng/ml, microvascular invasion and rejection needing anti‐lymphocytic antibodies. When considering pre‐transplant variables only, AFP level ≥400 ng/ml (HR = 5.13; P &lt; 0.0001) was the unique risk factor for recurrence; conversely, application of LRT was protective (HR = 0.42; P = 0.04). MC‐IN patients having LRT (n = 79) had the best 5‐year tumour‐free survival (TFS) (91.6%). MC‐IN patients without LRT (n = 16) and MC‐OUT patients with LRT (n = 30) had similar good TFS (72.7% vs.77.5%); finally MC‐OUT patients without LRT (n = 12) had the worst results (45.0%; vs. 1st group: P &lt; 0.0001). Immediate pre‐LT AFP and aggressive pre‐transplant LRT strategy, especially in MC‐OUT patients, are both important elements to further expand inclusion criteria without compromising long‐term results of HCC liver recipients.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>22716073</pmid><doi>10.1111/j.1432-2277.2012.01512.x</doi><tpages>9</tpages></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Adult
Aged
alpha-Fetoproteins - metabolism
alpha-foetoprotein
Combined Modality Therapy
downstaging
Female
hepatocellular cancer
Humans
Liver cancer
Liver cirrhosis
Liver Cirrhosis - complications
Liver Neoplasms - etiology
Liver Neoplasms - surgery
Liver Neoplasms - therapy
liver transplantation
Liver Transplantation - mortality
locoregional treatment
Male
Middle Aged
Multivariate analysis
Patient Selection
Pulsed Radiofrequency Treatment
Retrospective Studies
Transplants & implants
title Liver transplantation for hepatocellular cancer: UCL experience in 137 adult cirrhotic patients. Alpha-foetoprotein level and locoregional treatment as refined selection criteria
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