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...

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Veröffentlicht in:Liver transplantation 2014-08, Vol.20 (8), p.945-951
Hauptverfasser: Hameed, Bilal, Mehta, Neil, Sapisochin, Gonzalo, Roberts, John P., Yao, Francis Y.
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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.
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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 &lt; 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 &gt; 1000 ng/mL (HR = 4.5, 95% CI = 1.3‐15.3, P = 0.02), and an AFP level &gt; 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 &gt; 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 &gt; 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 &gt; 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 &gt; 1000 ng/mL may be a surrogate for vascular invasion and may be used to predict posttransplant HCC recurrence. Incorporating an AFP level &gt; 1000 ng/mL as an exclusion criterion for LT within the Milan criteria may further improve posttransplant outcomes. 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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 &lt; 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 &gt; 1000 ng/mL (HR = 4.5, 95% CI = 1.3‐15.3, P = 0.02), and an AFP level &gt; 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 &gt; 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 &gt; 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 &gt; 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 &gt; 1000 ng/mL may be a surrogate for vascular invasion and may be used to predict posttransplant HCC recurrence. Incorporating an AFP level &gt; 1000 ng/mL as an exclusion criterion for LT within the Milan criteria may further improve posttransplant outcomes. 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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 &gt; 1000 ng/mL as an exclusion criterion for liver transplantation in patients with hepatocellular carcinoma meeting the Milan criteria</title><author>Hameed, Bilal ; 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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 &amp; 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 &gt; 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 &lt; 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 &gt; 1000 ng/mL (HR = 4.5, 95% CI = 1.3‐15.3, P = 0.02), and an AFP level &gt; 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 &gt; 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 &gt; 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 &gt; 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 &gt; 1000 ng/mL may be a surrogate for vascular invasion and may be used to predict posttransplant HCC recurrence. Incorporating an AFP level &gt; 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>
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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
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