Alpha‐fetoprotein level > 1000 ng/mL as an exclusion criterion for liver transplantation in patients with hepatocellular carcinoma meeting the Milan criteria
Serum alpha‐fetoprotein (AFP) has been increasingly recognized as a marker for a poor prognosis after liver transplantation (LT) for hepatocellular carcinoma (HCC). Many published reports, however, have included a large proportion of patients with HCC beyond the Milan criteria, and the effects of in...
Gespeichert in:
Veröffentlicht in: | Liver transplantation 2014-08, Vol.20 (8), p.945-951 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 951 |
---|---|
container_issue | 8 |
container_start_page | 945 |
container_title | Liver transplantation |
container_volume | 20 |
creator | Hameed, Bilal Mehta, Neil Sapisochin, Gonzalo Roberts, John P. Yao, Francis Y. |
description | Serum alpha‐fetoprotein (AFP) has been increasingly recognized as a marker for a poor prognosis after liver transplantation (LT) for hepatocellular carcinoma (HCC). Many published reports, however, have included a large proportion of patients with HCC beyond the Milan criteria, and the effects of incorporating AFP as an exclusion criterion for LT remain unclear. We studied 211 consecutive patients undergoing LT for HCC within the Milan criteria according to imaging under the Model for End‐Stage Liver Disease organ allocation system between June 2002 and January 2009. The majority (93.4%) had locoregional therapy before LT. The median follow‐up was 4.5 years (minimum = 2 years). The Kaplan‐Meier 1‐ and 5‐year patient survival rates were 94.3% and 83.4%, respectively. In a univariate analysis, significant predictors of HCC recurrence included vascular invasion [hazard ratio (HR) = 10, 95% confidence interval (CI) = 3.9‐26, P 1000 ng/mL (HR = 4.5, 95% CI = 1.3‐15.3, P = 0.02), and an AFP level > 500 ng/mL (HR = 3.1, 95% CI = 1.04‐9.4, P = 0.04). In a multivariate analysis, vascular invasion was the only significant predictor of tumor recurrence (HR = 5.6, 95% CI = 1.9‐19, P = 0.02). An AFP level > 1000 ng/mL was the strongest pretransplant variable predicting vascular invasion (odds ratio = 6.8, 95% CI = 1.6‐19.1, P = 0.006). The 1‐ and 5‐year rates of survival without recurrence were 90% and 52.7%, respectively, for patients with an AFP level > 1000 ng/mL and 95% and 80.3%, respectively, for patients with an AFP level ≤ 1000 ng/mL (P = 0.026). Applying an AFP level > 1000 ng/mL as a cutoff would have resulted in the exclusion of 4.7% of the patients from LT and a 20% reduction in HCC recurrence. In conclusion, an AFP level > 1000 ng/mL may be a surrogate for vascular invasion and may be used to predict posttransplant HCC recurrence. Incorporating an AFP level > 1000 ng/mL as an exclusion criterion for LT within the Milan criteria may further improve posttransplant outcomes. Liver Transpl 20:945‐951, 2014. © 2014 AASLD. |
doi_str_mv | 10.1002/lt.23904 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4807739</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1550078590</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4384-44aab2bd9ab3896ba8678f1b7a58e45bef1f9d6cdbef3d8a74d0a64b8de0596f3</originalsourceid><addsrcrecordid>eNpdks1u1TAQhSNERUtB4gmQJTZs0tqJEzubSlUFBelWbMramiSTG1eOHWznlu66Zcc79M36JPj25wpYWHOs-XR0RjNZ9o7RI0ZpcWziUVE2lL_IDlhViLzmony503W1n70O4YpSxqqGvsr2Cy4aUUh2kN2dmnmE-9vfA0Y3exdRW2Jwg-b-9tdJesmfErs-nlYEAgFL8GdnlqCdJZ3XEf1WDc4TozfoSfRgw2zARojbTnKbk0IbA7nWcSQjpr_r0JjFgCcd-E5bNwGZEKO2axJHJBc6OTz7w5tsbwAT8O1TPcy-f_50efYlX307_3p2uso7Xkqecw7QFm3fQFvKpm5B1kIOrBVQSeRViwMbmr7u-qTKXoLgPYWat7JHWjX1UB5mJ4--89JO2HcptAejZq8n8DfKgVb_dqwe1dptFJdUiLJJBh-fDLz7sWCIatJhOypYdEtQrKooFTLtIKEf_kOv3OJtGi9RXMoysSJR7_9OtIvyvL8E5I_AtTZ4s-szqrZ3oUxUD3ehVpcPtfwDq0yxfA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1548831557</pqid></control><display><type>article</type><title>Alpha‐fetoprotein level > 1000 ng/mL as an exclusion criterion for liver transplantation in patients with hepatocellular carcinoma meeting the Milan criteria</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><source>Alma/SFX Local Collection</source><creator>Hameed, Bilal ; Mehta, Neil ; Sapisochin, Gonzalo ; Roberts, John P. ; Yao, Francis Y.</creator><creatorcontrib>Hameed, Bilal ; Mehta, Neil ; Sapisochin, Gonzalo ; Roberts, John P. ; Yao, Francis Y.</creatorcontrib><description>Serum alpha‐fetoprotein (AFP) has been increasingly recognized as a marker for a poor prognosis after liver transplantation (LT) for hepatocellular carcinoma (HCC). Many published reports, however, have included a large proportion of patients with HCC beyond the Milan criteria, and the effects of incorporating AFP as an exclusion criterion for LT remain unclear. We studied 211 consecutive patients undergoing LT for HCC within the Milan criteria according to imaging under the Model for End‐Stage Liver Disease organ allocation system between June 2002 and January 2009. The majority (93.4%) had locoregional therapy before LT. The median follow‐up was 4.5 years (minimum = 2 years). The Kaplan‐Meier 1‐ and 5‐year patient survival rates were 94.3% and 83.4%, respectively. In a univariate analysis, significant predictors of HCC recurrence included vascular invasion [hazard ratio (HR) = 10, 95% confidence interval (CI) = 3.9‐26, P < 0.001], a pathological tumor stage beyond the University of California San Francisco criteria (HR = 4.1, 95% CI = 1.36‐12.6, P = 0.01), an AFP level > 1000 ng/mL (HR = 4.5, 95% CI = 1.3‐15.3, P = 0.02), and an AFP level > 500 ng/mL (HR = 3.1, 95% CI = 1.04‐9.4, P = 0.04). In a multivariate analysis, vascular invasion was the only significant predictor of tumor recurrence (HR = 5.6, 95% CI = 1.9‐19, P = 0.02). An AFP level > 1000 ng/mL was the strongest pretransplant variable predicting vascular invasion (odds ratio = 6.8, 95% CI = 1.6‐19.1, P = 0.006). The 1‐ and 5‐year rates of survival without recurrence were 90% and 52.7%, respectively, for patients with an AFP level > 1000 ng/mL and 95% and 80.3%, respectively, for patients with an AFP level ≤ 1000 ng/mL (P = 0.026). Applying an AFP level > 1000 ng/mL as a cutoff would have resulted in the exclusion of 4.7% of the patients from LT and a 20% reduction in HCC recurrence. In conclusion, an AFP level > 1000 ng/mL may be a surrogate for vascular invasion and may be used to predict posttransplant HCC recurrence. Incorporating an AFP level > 1000 ng/mL as an exclusion criterion for LT within the Milan criteria may further improve posttransplant outcomes. Liver Transpl 20:945‐951, 2014. © 2014 AASLD.</description><identifier>ISSN: 1527-6465</identifier><identifier>EISSN: 1527-6473</identifier><identifier>DOI: 10.1002/lt.23904</identifier><identifier>PMID: 24797281</identifier><identifier>CODEN: LITRFO</identifier><language>eng</language><publisher>United States: Wolters Kluwer Health, Inc</publisher><subject>Adult ; Aged ; alpha-Fetoproteins - metabolism ; Carcinoma, Hepatocellular - blood ; Carcinoma, Hepatocellular - mortality ; Carcinoma, Hepatocellular - surgery ; Confidence intervals ; End Stage Liver Disease - diagnosis ; Female ; Humans ; Kaplan-Meier Estimate ; Liver cancer ; Liver cirrhosis ; Liver Neoplasms - blood ; Liver Neoplasms - mortality ; Liver Neoplasms - surgery ; Liver Transplantation - standards ; Male ; Medical prognosis ; Middle Aged ; Multivariate Analysis ; Neoplasm Recurrence, Local - diagnosis ; Odds Ratio ; Prognosis ; Proportional Hazards Models ; Risk Factors ; Transplants & implants ; Treatment Outcome ; Young Adult</subject><ispartof>Liver transplantation, 2014-08, Vol.20 (8), p.945-951</ispartof><rights>2014 American Association for the Study of Liver Diseases</rights><rights>2014 American Association for the Study of Liver Diseases.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4384-44aab2bd9ab3896ba8678f1b7a58e45bef1f9d6cdbef3d8a74d0a64b8de0596f3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Flt.23904$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Flt.23904$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24797281$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hameed, Bilal</creatorcontrib><creatorcontrib>Mehta, Neil</creatorcontrib><creatorcontrib>Sapisochin, Gonzalo</creatorcontrib><creatorcontrib>Roberts, John P.</creatorcontrib><creatorcontrib>Yao, Francis Y.</creatorcontrib><title>Alpha‐fetoprotein level > 1000 ng/mL as an exclusion criterion for liver transplantation in patients with hepatocellular carcinoma meeting the Milan criteria</title><title>Liver transplantation</title><addtitle>Liver Transpl</addtitle><description>Serum alpha‐fetoprotein (AFP) has been increasingly recognized as a marker for a poor prognosis after liver transplantation (LT) for hepatocellular carcinoma (HCC). Many published reports, however, have included a large proportion of patients with HCC beyond the Milan criteria, and the effects of incorporating AFP as an exclusion criterion for LT remain unclear. We studied 211 consecutive patients undergoing LT for HCC within the Milan criteria according to imaging under the Model for End‐Stage Liver Disease organ allocation system between June 2002 and January 2009. The majority (93.4%) had locoregional therapy before LT. The median follow‐up was 4.5 years (minimum = 2 years). The Kaplan‐Meier 1‐ and 5‐year patient survival rates were 94.3% and 83.4%, respectively. In a univariate analysis, significant predictors of HCC recurrence included vascular invasion [hazard ratio (HR) = 10, 95% confidence interval (CI) = 3.9‐26, P < 0.001], a pathological tumor stage beyond the University of California San Francisco criteria (HR = 4.1, 95% CI = 1.36‐12.6, P = 0.01), an AFP level > 1000 ng/mL (HR = 4.5, 95% CI = 1.3‐15.3, P = 0.02), and an AFP level > 500 ng/mL (HR = 3.1, 95% CI = 1.04‐9.4, P = 0.04). In a multivariate analysis, vascular invasion was the only significant predictor of tumor recurrence (HR = 5.6, 95% CI = 1.9‐19, P = 0.02). An AFP level > 1000 ng/mL was the strongest pretransplant variable predicting vascular invasion (odds ratio = 6.8, 95% CI = 1.6‐19.1, P = 0.006). The 1‐ and 5‐year rates of survival without recurrence were 90% and 52.7%, respectively, for patients with an AFP level > 1000 ng/mL and 95% and 80.3%, respectively, for patients with an AFP level ≤ 1000 ng/mL (P = 0.026). Applying an AFP level > 1000 ng/mL as a cutoff would have resulted in the exclusion of 4.7% of the patients from LT and a 20% reduction in HCC recurrence. In conclusion, an AFP level > 1000 ng/mL may be a surrogate for vascular invasion and may be used to predict posttransplant HCC recurrence. Incorporating an AFP level > 1000 ng/mL as an exclusion criterion for LT within the Milan criteria may further improve posttransplant outcomes. Liver Transpl 20:945‐951, 2014. © 2014 AASLD.</description><subject>Adult</subject><subject>Aged</subject><subject>alpha-Fetoproteins - metabolism</subject><subject>Carcinoma, Hepatocellular - blood</subject><subject>Carcinoma, Hepatocellular - mortality</subject><subject>Carcinoma, Hepatocellular - surgery</subject><subject>Confidence intervals</subject><subject>End Stage Liver Disease - diagnosis</subject><subject>Female</subject><subject>Humans</subject><subject>Kaplan-Meier Estimate</subject><subject>Liver cancer</subject><subject>Liver cirrhosis</subject><subject>Liver Neoplasms - blood</subject><subject>Liver Neoplasms - mortality</subject><subject>Liver Neoplasms - surgery</subject><subject>Liver Transplantation - standards</subject><subject>Male</subject><subject>Medical prognosis</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>Neoplasm Recurrence, Local - diagnosis</subject><subject>Odds Ratio</subject><subject>Prognosis</subject><subject>Proportional Hazards Models</subject><subject>Risk Factors</subject><subject>Transplants & implants</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>1527-6465</issn><issn>1527-6473</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdks1u1TAQhSNERUtB4gmQJTZs0tqJEzubSlUFBelWbMramiSTG1eOHWznlu66Zcc79M36JPj25wpYWHOs-XR0RjNZ9o7RI0ZpcWziUVE2lL_IDlhViLzmony503W1n70O4YpSxqqGvsr2Cy4aUUh2kN2dmnmE-9vfA0Y3exdRW2Jwg-b-9tdJesmfErs-nlYEAgFL8GdnlqCdJZ3XEf1WDc4TozfoSfRgw2zARojbTnKbk0IbA7nWcSQjpr_r0JjFgCcd-E5bNwGZEKO2axJHJBc6OTz7w5tsbwAT8O1TPcy-f_50efYlX307_3p2uso7Xkqecw7QFm3fQFvKpm5B1kIOrBVQSeRViwMbmr7u-qTKXoLgPYWat7JHWjX1UB5mJ4--89JO2HcptAejZq8n8DfKgVb_dqwe1dptFJdUiLJJBh-fDLz7sWCIatJhOypYdEtQrKooFTLtIKEf_kOv3OJtGi9RXMoysSJR7_9OtIvyvL8E5I_AtTZ4s-szqrZ3oUxUD3ehVpcPtfwDq0yxfA</recordid><startdate>201408</startdate><enddate>201408</enddate><creator>Hameed, Bilal</creator><creator>Mehta, Neil</creator><creator>Sapisochin, Gonzalo</creator><creator>Roberts, John P.</creator><creator>Yao, Francis Y.</creator><general>Wolters Kluwer Health, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>K9.</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201408</creationdate><title>Alpha‐fetoprotein level > 1000 ng/mL as an exclusion criterion for liver transplantation in patients with hepatocellular carcinoma meeting the Milan criteria</title><author>Hameed, Bilal ; Mehta, Neil ; Sapisochin, Gonzalo ; Roberts, John P. ; Yao, Francis Y.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4384-44aab2bd9ab3896ba8678f1b7a58e45bef1f9d6cdbef3d8a74d0a64b8de0596f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>Aged</topic><topic>alpha-Fetoproteins - metabolism</topic><topic>Carcinoma, Hepatocellular - blood</topic><topic>Carcinoma, Hepatocellular - mortality</topic><topic>Carcinoma, Hepatocellular - surgery</topic><topic>Confidence intervals</topic><topic>End Stage Liver Disease - diagnosis</topic><topic>Female</topic><topic>Humans</topic><topic>Kaplan-Meier Estimate</topic><topic>Liver cancer</topic><topic>Liver cirrhosis</topic><topic>Liver Neoplasms - blood</topic><topic>Liver Neoplasms - mortality</topic><topic>Liver Neoplasms - surgery</topic><topic>Liver Transplantation - standards</topic><topic>Male</topic><topic>Medical prognosis</topic><topic>Middle Aged</topic><topic>Multivariate Analysis</topic><topic>Neoplasm Recurrence, Local - diagnosis</topic><topic>Odds Ratio</topic><topic>Prognosis</topic><topic>Proportional Hazards Models</topic><topic>Risk Factors</topic><topic>Transplants & implants</topic><topic>Treatment Outcome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hameed, Bilal</creatorcontrib><creatorcontrib>Mehta, Neil</creatorcontrib><creatorcontrib>Sapisochin, Gonzalo</creatorcontrib><creatorcontrib>Roberts, John P.</creatorcontrib><creatorcontrib>Yao, Francis Y.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Liver transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hameed, Bilal</au><au>Mehta, Neil</au><au>Sapisochin, Gonzalo</au><au>Roberts, John P.</au><au>Yao, Francis Y.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Alpha‐fetoprotein level > 1000 ng/mL as an exclusion criterion for liver transplantation in patients with hepatocellular carcinoma meeting the Milan criteria</atitle><jtitle>Liver transplantation</jtitle><addtitle>Liver Transpl</addtitle><date>2014-08</date><risdate>2014</risdate><volume>20</volume><issue>8</issue><spage>945</spage><epage>951</epage><pages>945-951</pages><issn>1527-6465</issn><eissn>1527-6473</eissn><coden>LITRFO</coden><abstract>Serum alpha‐fetoprotein (AFP) has been increasingly recognized as a marker for a poor prognosis after liver transplantation (LT) for hepatocellular carcinoma (HCC). Many published reports, however, have included a large proportion of patients with HCC beyond the Milan criteria, and the effects of incorporating AFP as an exclusion criterion for LT remain unclear. We studied 211 consecutive patients undergoing LT for HCC within the Milan criteria according to imaging under the Model for End‐Stage Liver Disease organ allocation system between June 2002 and January 2009. The majority (93.4%) had locoregional therapy before LT. The median follow‐up was 4.5 years (minimum = 2 years). The Kaplan‐Meier 1‐ and 5‐year patient survival rates were 94.3% and 83.4%, respectively. In a univariate analysis, significant predictors of HCC recurrence included vascular invasion [hazard ratio (HR) = 10, 95% confidence interval (CI) = 3.9‐26, P < 0.001], a pathological tumor stage beyond the University of California San Francisco criteria (HR = 4.1, 95% CI = 1.36‐12.6, P = 0.01), an AFP level > 1000 ng/mL (HR = 4.5, 95% CI = 1.3‐15.3, P = 0.02), and an AFP level > 500 ng/mL (HR = 3.1, 95% CI = 1.04‐9.4, P = 0.04). In a multivariate analysis, vascular invasion was the only significant predictor of tumor recurrence (HR = 5.6, 95% CI = 1.9‐19, P = 0.02). An AFP level > 1000 ng/mL was the strongest pretransplant variable predicting vascular invasion (odds ratio = 6.8, 95% CI = 1.6‐19.1, P = 0.006). The 1‐ and 5‐year rates of survival without recurrence were 90% and 52.7%, respectively, for patients with an AFP level > 1000 ng/mL and 95% and 80.3%, respectively, for patients with an AFP level ≤ 1000 ng/mL (P = 0.026). Applying an AFP level > 1000 ng/mL as a cutoff would have resulted in the exclusion of 4.7% of the patients from LT and a 20% reduction in HCC recurrence. In conclusion, an AFP level > 1000 ng/mL may be a surrogate for vascular invasion and may be used to predict posttransplant HCC recurrence. Incorporating an AFP level > 1000 ng/mL as an exclusion criterion for LT within the Milan criteria may further improve posttransplant outcomes. Liver Transpl 20:945‐951, 2014. © 2014 AASLD.</abstract><cop>United States</cop><pub>Wolters Kluwer Health, Inc</pub><pmid>24797281</pmid><doi>10.1002/lt.23904</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1527-6465 |
ispartof | Liver transplantation, 2014-08, Vol.20 (8), p.945-951 |
issn | 1527-6465 1527-6473 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4807739 |
source | MEDLINE; Wiley Online Library Journals Frontfile Complete; Alma/SFX Local Collection |
subjects | Adult Aged alpha-Fetoproteins - metabolism Carcinoma, Hepatocellular - blood Carcinoma, Hepatocellular - mortality Carcinoma, Hepatocellular - surgery Confidence intervals End Stage Liver Disease - diagnosis Female Humans Kaplan-Meier Estimate Liver cancer Liver cirrhosis Liver Neoplasms - blood Liver Neoplasms - mortality Liver Neoplasms - surgery Liver Transplantation - standards Male Medical prognosis Middle Aged Multivariate Analysis Neoplasm Recurrence, Local - diagnosis Odds Ratio Prognosis Proportional Hazards Models Risk Factors Transplants & implants Treatment Outcome Young Adult |
title | Alpha‐fetoprotein level > 1000 ng/mL as an exclusion criterion for liver transplantation in patients with hepatocellular carcinoma meeting the Milan criteria |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-30T17%3A13%3A40IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Alpha%E2%80%90fetoprotein%20level%E2%80%89%3E%E2%80%891000%20ng/mL%20as%20an%20exclusion%20criterion%20for%20liver%20transplantation%20in%20patients%20with%20hepatocellular%20carcinoma%20meeting%20the%20Milan%20criteria&rft.jtitle=Liver%20transplantation&rft.au=Hameed,%20Bilal&rft.date=2014-08&rft.volume=20&rft.issue=8&rft.spage=945&rft.epage=951&rft.pages=945-951&rft.issn=1527-6465&rft.eissn=1527-6473&rft.coden=LITRFO&rft_id=info:doi/10.1002/lt.23904&rft_dat=%3Cproquest_pubme%3E1550078590%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1548831557&rft_id=info:pmid/24797281&rfr_iscdi=true |