Quantitation of alpha-fetoprotein messenger RNA for early detection of recurrent hepatocellular carcinoma: A prospective pilot study
Background: Alpha-fetoprotein (AFP) messenger RNA (mRNA) may be a potential marker of the dissemination of hepatocellular carcinoma (HCC) cells into the circulation. The aim of this prospective pilot study was to assess the prognostic value of quantitative levels of AFP mRNA in patients undergoing a...
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description | Background: Alpha-fetoprotein (AFP) messenger RNA (mRNA) may be a potential marker of the dissemination of hepatocellular carcinoma (HCC) cells into the circulation. The aim of this prospective pilot study was to assess the prognostic value of quantitative levels of AFP mRNA in patients undergoing ablative treatment for HCC.
Methods: Peripheral blood samples were taken from seven patients before and after treatment for measurement of AFP mRNA levels by reverse-transcriptase polymerase chain reaction (RT-PCR). Patients were treated with percutaneous radiofrequency thermal ablation (
n
=
3) or transarterial chemoembolization (
n
=
4). The level of AFP mRNA in blood was serially determined, and the time course was related to the clinical course and disease outcome. The median duration of follow-up was 14 months (range, 9–16 months).
Results: HCC recurred locally in four patients, and lung metastases developed in two of them. Patients were divided into three groups on the basis of the pre- and post-treatment AFP mRNA status. Group 1 included four patients with consistently high serum AFP and AFP mRNA levels (pre- and post-treatment). These patients developed distant and local recurrence. Group 2 included a patient with serum-negative AFP mRNA and normal AFP levels at entry. Although serum AFP remained within normal range, mean AFP mRNA increased from 10 to 95
copies/μg RNA. This patient had no distant metastases, but his tumor markedly increased in size. In Group 3, AFP mRNA and serum AFP remained within normal range before and after treatment. These two patients did not develop either local or distant metastases during the follow-up period.
Conclusions: Although this is a small sample size pilot study these findings imply that quantitative measurement of AFP-expressing cells in peripheral blood may serve as a marker of HCC recurrence. |
doi_str_mv | 10.1016/j.cdp.2005.12.003 |
format | Article |
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Methods: Peripheral blood samples were taken from seven patients before and after treatment for measurement of AFP mRNA levels by reverse-transcriptase polymerase chain reaction (RT-PCR). Patients were treated with percutaneous radiofrequency thermal ablation (
n
=
3) or transarterial chemoembolization (
n
=
4). The level of AFP mRNA in blood was serially determined, and the time course was related to the clinical course and disease outcome. The median duration of follow-up was 14 months (range, 9–16 months).
Results: HCC recurred locally in four patients, and lung metastases developed in two of them. Patients were divided into three groups on the basis of the pre- and post-treatment AFP mRNA status. Group 1 included four patients with consistently high serum AFP and AFP mRNA levels (pre- and post-treatment). These patients developed distant and local recurrence. Group 2 included a patient with serum-negative AFP mRNA and normal AFP levels at entry. Although serum AFP remained within normal range, mean AFP mRNA increased from 10 to 95
copies/μg RNA. This patient had no distant metastases, but his tumor markedly increased in size. In Group 3, AFP mRNA and serum AFP remained within normal range before and after treatment. These two patients did not develop either local or distant metastases during the follow-up period.
Conclusions: Although this is a small sample size pilot study these findings imply that quantitative measurement of AFP-expressing cells in peripheral blood may serve as a marker of HCC recurrence.</description><identifier>ISSN: 0361-090X</identifier><identifier>ISSN: 1877-7821</identifier><identifier>EISSN: 1873-443X</identifier><identifier>EISSN: 1877-783X</identifier><identifier>DOI: 10.1016/j.cdp.2005.12.003</identifier><identifier>PMID: 16638626</identifier><identifier>CODEN: CDPRD4</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Ablative treatment ; Aged ; Alanine aminotransferase ; Alpha-fetoprotein ; alpha-Fetoproteins - analysis ; Aspartate aminotransferase ; Cancer ; Carcinoma, Hepatocellular - blood ; Carcinoma, Hepatocellular - diagnosis ; Carcinoma, Hepatocellular - secondary ; Carcinoma, Hepatocellular - therapy ; Catheter Ablation ; Cirrhosis ; Embolization, Therapeutic ; Epidemiology ; Female ; Hepatitis B surface antigen ; Hepatitis C virus ; Hepatocellular carcinoma ; Humans ; Liver cancer ; Liver Neoplasms - blood ; Liver Neoplasms - diagnosis ; Liver Neoplasms - therapy ; Male ; Medical imaging ; Messenger RNA ; Neoplasm Recurrence, Local - blood ; Neoplasm Recurrence, Local - diagnosis ; Patients ; Pilot Projects ; Prognosis ; Prospective Studies ; Quantitative PCR ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Messenger - blood ; Tumor differentiation ; Tumor size ; Tumor-node metastasis ; Tumors</subject><ispartof>Cancer detection and prevention, 2006-01, Vol.30 (2), p.204-209</ispartof><rights>2006 International Society for Preventive Oncology</rights><rights>Copyright Elsevier Limited 2006</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c379t-4473414ec36679f2c4d100a9f6a6d284ea16907bac27aeed66861d899c06be1d3</citedby><cites>FETCH-LOGICAL-c379t-4473414ec36679f2c4d100a9f6a6d284ea16907bac27aeed66861d899c06be1d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16638626$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schmilovitz-Weiss, H.</creatorcontrib><creatorcontrib>Stemmer, S.M.</creatorcontrib><creatorcontrib>Liberzon, E.</creatorcontrib><creatorcontrib>Avigad, S.</creatorcontrib><creatorcontrib>Sulkes, J.</creatorcontrib><creatorcontrib>Belinki, A.</creatorcontrib><creatorcontrib>Kazatsker, A.</creatorcontrib><creatorcontrib>Ben-Ari, Z.</creatorcontrib><title>Quantitation of alpha-fetoprotein messenger RNA for early detection of recurrent hepatocellular carcinoma: A prospective pilot study</title><title>Cancer detection and prevention</title><addtitle>Cancer Detect Prev</addtitle><description>Background: Alpha-fetoprotein (AFP) messenger RNA (mRNA) may be a potential marker of the dissemination of hepatocellular carcinoma (HCC) cells into the circulation. The aim of this prospective pilot study was to assess the prognostic value of quantitative levels of AFP mRNA in patients undergoing ablative treatment for HCC.
Methods: Peripheral blood samples were taken from seven patients before and after treatment for measurement of AFP mRNA levels by reverse-transcriptase polymerase chain reaction (RT-PCR). Patients were treated with percutaneous radiofrequency thermal ablation (
n
=
3) or transarterial chemoembolization (
n
=
4). The level of AFP mRNA in blood was serially determined, and the time course was related to the clinical course and disease outcome. The median duration of follow-up was 14 months (range, 9–16 months).
Results: HCC recurred locally in four patients, and lung metastases developed in two of them. Patients were divided into three groups on the basis of the pre- and post-treatment AFP mRNA status. Group 1 included four patients with consistently high serum AFP and AFP mRNA levels (pre- and post-treatment). These patients developed distant and local recurrence. Group 2 included a patient with serum-negative AFP mRNA and normal AFP levels at entry. Although serum AFP remained within normal range, mean AFP mRNA increased from 10 to 95
copies/μg RNA. This patient had no distant metastases, but his tumor markedly increased in size. In Group 3, AFP mRNA and serum AFP remained within normal range before and after treatment. These two patients did not develop either local or distant metastases during the follow-up period.
Conclusions: Although this is a small sample size pilot study these findings imply that quantitative measurement of AFP-expressing cells in peripheral blood may serve as a marker of HCC recurrence.</description><subject>Ablative treatment</subject><subject>Aged</subject><subject>Alanine aminotransferase</subject><subject>Alpha-fetoprotein</subject><subject>alpha-Fetoproteins - analysis</subject><subject>Aspartate aminotransferase</subject><subject>Cancer</subject><subject>Carcinoma, Hepatocellular - blood</subject><subject>Carcinoma, Hepatocellular - diagnosis</subject><subject>Carcinoma, Hepatocellular - secondary</subject><subject>Carcinoma, Hepatocellular - therapy</subject><subject>Catheter Ablation</subject><subject>Cirrhosis</subject><subject>Embolization, Therapeutic</subject><subject>Epidemiology</subject><subject>Female</subject><subject>Hepatitis B surface antigen</subject><subject>Hepatitis C virus</subject><subject>Hepatocellular carcinoma</subject><subject>Humans</subject><subject>Liver cancer</subject><subject>Liver Neoplasms - blood</subject><subject>Liver Neoplasms - diagnosis</subject><subject>Liver Neoplasms - therapy</subject><subject>Male</subject><subject>Medical imaging</subject><subject>Messenger RNA</subject><subject>Neoplasm Recurrence, Local - blood</subject><subject>Neoplasm Recurrence, Local - diagnosis</subject><subject>Patients</subject><subject>Pilot Projects</subject><subject>Prognosis</subject><subject>Prospective Studies</subject><subject>Quantitative PCR</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Messenger - blood</subject><subject>Tumor differentiation</subject><subject>Tumor size</subject><subject>Tumor-node metastasis</subject><subject>Tumors</subject><issn>0361-090X</issn><issn>1877-7821</issn><issn>1873-443X</issn><issn>1877-783X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9kU9r3DAUxEVoSTZpP0AvRVDIzY5kOc92e1pC8wdCQ0ILuQmt9NxosSVXkgN7zwevlt1SyCGnd_nNMPOGkE-clZxxOFuX2kxlxdh5yauSMXFAFrxtRFHX4vEdWTABvGAdezwixzGuWdZ0Ag7JEQcQLVSwIC_3s3LJJpWsd9T3VA3Tkyp6TH4KPqF1dMQY0f3GQB9-LGnvA0UVhg01mFD_kwXUcwjoEn3CSSWvcRjmQQWqVdDW-VF9pUuaLeO0FT0jnezgE41pNpsP5H2vhogf9_eE_Lr8_vPiuri9u7q5WN4WWjRdyq0aUfMatQBour7SteGMqa4HBaZqa1S5H2tWSleNQjQALXDTdp1msEJuxAk53fnmHH9mjEmONm6TKod-jhJaxhs47zL45RW49nNwOZvkNW8BKtZApviO0rlWDNjLKdhRhY3kTG4HkmuZB5LbgSSvZB4oaz7vnefViOa_Yr9IBr7tAMyPeLYYZNQWnUZj84-TNN6-Yf8X3LejHA</recordid><startdate>20060101</startdate><enddate>20060101</enddate><creator>Schmilovitz-Weiss, H.</creator><creator>Stemmer, S.M.</creator><creator>Liberzon, E.</creator><creator>Avigad, S.</creator><creator>Sulkes, J.</creator><creator>Belinki, A.</creator><creator>Kazatsker, A.</creator><creator>Ben-Ari, Z.</creator><general>Elsevier Ltd</general><general>Elsevier Limited</general><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>3V.</scope><scope>7RV</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88C</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20060101</creationdate><title>Quantitation of alpha-fetoprotein messenger RNA for early detection of recurrent hepatocellular carcinoma: A prospective pilot study</title><author>Schmilovitz-Weiss, H. ; Stemmer, S.M. ; Liberzon, E. ; Avigad, S. ; Sulkes, J. ; Belinki, A. ; Kazatsker, A. ; Ben-Ari, Z.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c379t-4473414ec36679f2c4d100a9f6a6d284ea16907bac27aeed66861d899c06be1d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Ablative treatment</topic><topic>Aged</topic><topic>Alanine aminotransferase</topic><topic>Alpha-fetoprotein</topic><topic>alpha-Fetoproteins - analysis</topic><topic>Aspartate aminotransferase</topic><topic>Cancer</topic><topic>Carcinoma, Hepatocellular - blood</topic><topic>Carcinoma, Hepatocellular - diagnosis</topic><topic>Carcinoma, Hepatocellular - secondary</topic><topic>Carcinoma, Hepatocellular - therapy</topic><topic>Catheter Ablation</topic><topic>Cirrhosis</topic><topic>Embolization, Therapeutic</topic><topic>Epidemiology</topic><topic>Female</topic><topic>Hepatitis B surface antigen</topic><topic>Hepatitis C virus</topic><topic>Hepatocellular carcinoma</topic><topic>Humans</topic><topic>Liver cancer</topic><topic>Liver Neoplasms - blood</topic><topic>Liver Neoplasms - diagnosis</topic><topic>Liver Neoplasms - therapy</topic><topic>Male</topic><topic>Medical imaging</topic><topic>Messenger RNA</topic><topic>Neoplasm Recurrence, Local - blood</topic><topic>Neoplasm Recurrence, Local - diagnosis</topic><topic>Patients</topic><topic>Pilot Projects</topic><topic>Prognosis</topic><topic>Prospective Studies</topic><topic>Quantitative PCR</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Messenger - blood</topic><topic>Tumor differentiation</topic><topic>Tumor size</topic><topic>Tumor-node metastasis</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schmilovitz-Weiss, H.</creatorcontrib><creatorcontrib>Stemmer, S.M.</creatorcontrib><creatorcontrib>Liberzon, E.</creatorcontrib><creatorcontrib>Avigad, S.</creatorcontrib><creatorcontrib>Sulkes, J.</creatorcontrib><creatorcontrib>Belinki, A.</creatorcontrib><creatorcontrib>Kazatsker, A.</creatorcontrib><creatorcontrib>Ben-Ari, Z.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer detection and prevention</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schmilovitz-Weiss, H.</au><au>Stemmer, S.M.</au><au>Liberzon, E.</au><au>Avigad, S.</au><au>Sulkes, J.</au><au>Belinki, A.</au><au>Kazatsker, A.</au><au>Ben-Ari, Z.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantitation of alpha-fetoprotein messenger RNA for early detection of recurrent hepatocellular carcinoma: A prospective pilot study</atitle><jtitle>Cancer detection and prevention</jtitle><addtitle>Cancer Detect Prev</addtitle><date>2006-01-01</date><risdate>2006</risdate><volume>30</volume><issue>2</issue><spage>204</spage><epage>209</epage><pages>204-209</pages><issn>0361-090X</issn><issn>1877-7821</issn><eissn>1873-443X</eissn><eissn>1877-783X</eissn><coden>CDPRD4</coden><abstract>Background: Alpha-fetoprotein (AFP) messenger RNA (mRNA) may be a potential marker of the dissemination of hepatocellular carcinoma (HCC) cells into the circulation. The aim of this prospective pilot study was to assess the prognostic value of quantitative levels of AFP mRNA in patients undergoing ablative treatment for HCC.
Methods: Peripheral blood samples were taken from seven patients before and after treatment for measurement of AFP mRNA levels by reverse-transcriptase polymerase chain reaction (RT-PCR). Patients were treated with percutaneous radiofrequency thermal ablation (
n
=
3) or transarterial chemoembolization (
n
=
4). The level of AFP mRNA in blood was serially determined, and the time course was related to the clinical course and disease outcome. The median duration of follow-up was 14 months (range, 9–16 months).
Results: HCC recurred locally in four patients, and lung metastases developed in two of them. Patients were divided into three groups on the basis of the pre- and post-treatment AFP mRNA status. Group 1 included four patients with consistently high serum AFP and AFP mRNA levels (pre- and post-treatment). These patients developed distant and local recurrence. Group 2 included a patient with serum-negative AFP mRNA and normal AFP levels at entry. Although serum AFP remained within normal range, mean AFP mRNA increased from 10 to 95
copies/μg RNA. This patient had no distant metastases, but his tumor markedly increased in size. In Group 3, AFP mRNA and serum AFP remained within normal range before and after treatment. These two patients did not develop either local or distant metastases during the follow-up period.
Conclusions: Although this is a small sample size pilot study these findings imply that quantitative measurement of AFP-expressing cells in peripheral blood may serve as a marker of HCC recurrence.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>16638626</pmid><doi>10.1016/j.cdp.2005.12.003</doi><tpages>6</tpages></addata></record> |
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subjects | Ablative treatment Aged Alanine aminotransferase Alpha-fetoprotein alpha-Fetoproteins - analysis Aspartate aminotransferase Cancer Carcinoma, Hepatocellular - blood Carcinoma, Hepatocellular - diagnosis Carcinoma, Hepatocellular - secondary Carcinoma, Hepatocellular - therapy Catheter Ablation Cirrhosis Embolization, Therapeutic Epidemiology Female Hepatitis B surface antigen Hepatitis C virus Hepatocellular carcinoma Humans Liver cancer Liver Neoplasms - blood Liver Neoplasms - diagnosis Liver Neoplasms - therapy Male Medical imaging Messenger RNA Neoplasm Recurrence, Local - blood Neoplasm Recurrence, Local - diagnosis Patients Pilot Projects Prognosis Prospective Studies Quantitative PCR Reverse Transcriptase Polymerase Chain Reaction RNA, Messenger - blood Tumor differentiation Tumor size Tumor-node metastasis Tumors |
title | Quantitation of alpha-fetoprotein messenger RNA for early detection of recurrent hepatocellular carcinoma: A prospective pilot study |
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