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Prevention of hepatocellular carcinoma: beyond hepatitis B vaccination

DC Field Value Language
dc.contributor.author김미나-
dc.contributor.author안상훈-
dc.contributor.author한광협-
dc.date.accessioned2018-03-26T16:48:31Z-
dc.date.available2018-03-26T16:48:31Z-
dc.date.issued2015-
dc.identifier.issn0093-7754-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/156837-
dc.description.abstractChronic hepatitis B (CHB) infection is the major cause of hepatocellular carcinoma (HCC), accounting for approximately 50% of the underlying etiologies. We reviewed the primary, secondary, and tertiary measures for the prevention of hepatitis B virus (HBV)-related HCC. The most effective method for preventing HBV-related HCC is vaccination. Universal hepatitis B vaccination has been shown to reduce the rates of HBV infection and HCC significantly. Once chronic HBV infection is established, antiviral treatment using interferon or nucleos(t)ide analogs is used to prevent disease progression to cirrhosis, HCC, or both. Studies have found viral replication indicated by HBV DNA level to be a strong risk factor for development of HCC. Additionally, periodic surveillance using ultrasonography and serum α-fetoprotein for earlier detection of HCC is also important so that curative treatments with survival benefit can be possible. Finally, adjuvant antiviral treatment using interferon or nucleos(t)ide analogs is used to prevent tumor recurrence after curative resection. Adjuvant interferon treatment prevented early recurrence, not late recurrence, probably due to its antiangiogenetic and antiproliferative effects. Adjuvant nucleos(t)ide analogs demonstrated promising results for preventing late recurrence, probably due to effective suppression of viral replication. Further investigations are required to establish the optimal preventive plans for HBV-related HCC.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherW.B. Saunders-
dc.relation.isPartOfSEMINARS IN ONCOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAntiviral Agents/therapeutic use-
dc.subject.MESHCarcinoma, Hepatocellular/prevention & control*-
dc.subject.MESHCarcinoma, Hepatocellular/virology*-
dc.subject.MESHHepatitis B, Chronic/complications*-
dc.subject.MESHHumans-
dc.subject.MESHLiver Neoplasms/prevention & control*-
dc.subject.MESHLiver Neoplasms/virology*-
dc.subject.MESHMass Screening-
dc.subject.MESHViral Hepatitis Vaccines/therapeutic use*-
dc.titlePrevention of hepatocellular carcinoma: beyond hepatitis B vaccination-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Internal Medicine-
dc.contributor.googleauthorMi Na Kim-
dc.contributor.googleauthorKwang-Hyub Han-
dc.contributor.googleauthorSang Hoon Ahn-
dc.identifier.doi10.1053/j.seminoncol.2014.12.018-
dc.contributor.localIdA00440-
dc.contributor.localIdA02226-
dc.contributor.localIdA04268-
dc.relation.journalcodeJ02938-
dc.identifier.eissn1532-8708-
dc.identifier.pmid25843736-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S0093775414002899-
dc.contributor.alternativeNameKim, Mi Na-
dc.contributor.alternativeNameAhn, Sang Hoon-
dc.contributor.alternativeNameHan, Kwang Hyup-
dc.contributor.affiliatedAuthorKim, Mi Na-
dc.contributor.affiliatedAuthorAhn, Sang Hoon-
dc.contributor.affiliatedAuthorHan, Kwang Hyup-
dc.citation.volume42-
dc.citation.number2-
dc.citation.startPage316-
dc.citation.endPage328-
dc.identifier.bibliographicCitationSEMINARS IN ONCOLOGY, Vol.42(2) : 316-328, 2015-
dc.identifier.rimsid39965-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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