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Reduced Risk of Hepatocellular Carcinoma in Patients with Chronic Hepatitis B Receiving Long-Term Besifovir Therapy

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dc.contributor.author안상훈-
dc.date.accessioned2025-02-03T08:52:00Z-
dc.date.available2025-02-03T08:52:00Z-
dc.date.issued2024-02-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/201943-
dc.description.abstractNo information is available regarding the influence of besifovir (BSV), a new nucleotide analogue, on the occurrence of hepatocellular carcinoma (HCC) in patients with chronic hepatitis B (CHB). This study evaluated the reduced risk of HCC in patients undergoing BSV treatment. A total of 188 patients with CHB were treated with BSV for up to 8 years. We prospectively assessed the incidence of HCC compared with the risk from prediction models. During the follow-up, 5 patients developed HCC: 1 of 139 patients with non-cirrhotic CHB, and 4 of 49 patients with liver cirrhosis. We compared the HCC incidence in non-cirrhotic and cirrhotic patients with the predicted number derived from the REACH-B (risk estimation for HCC in CHB) model and GAG-HCC (guide with age, gender, HBV DNA, core promotor mutation, and cirrhosis) model, respectively. The standardized incidence ratio (SIR) was 0.128 (p = 0.039) at 7 years in non-cirrhotic CHB patients, and the SIR was 0.371 (p = 0.047) at 7.5 years in cirrhotic patients, suggesting a significantly decreased HCC incidence in both groups. HCC prediction was available for BSV-treated patients using existing models. In conclusion, BSV decreased the risk of HCC in patients with CHB, and prediction models were applicable. Clinical trial registry website and trial number: ClinicalTrials.gov no: NCT01937806.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherMDPI-
dc.relation.isPartOfCANCERS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleReduced Risk of Hepatocellular Carcinoma in Patients with Chronic Hepatitis B Receiving Long-Term Besifovir Therapy-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorHyung Joon Yim-
dc.contributor.googleauthorSeong Hee Kang-
dc.contributor.googleauthorYoung Kul Jung-
dc.contributor.googleauthorSang Hoon Ahn-
dc.contributor.googleauthorWon Kim-
dc.contributor.googleauthorJin Mo Yang-
dc.contributor.googleauthorJae Young Jang-
dc.contributor.googleauthorYong Oh Kweon-
dc.contributor.googleauthorYong Kyun Cho-
dc.contributor.googleauthorYoon Jun Kim-
dc.contributor.googleauthorGun Young Hong-
dc.contributor.googleauthorDong Joon Kim-
dc.contributor.googleauthorJoo Hyun Sohn-
dc.contributor.googleauthorJin Woo Lee-
dc.contributor.googleauthorSung Jae Park-
dc.contributor.googleauthorSun Young Yim-
dc.contributor.googleauthorJin Kyung Park-
dc.contributor.googleauthorSoon Ho Um-
dc.identifier.doi10.3390/cancers16050887-
dc.contributor.localIdA02226-
dc.relation.journalcodeJ03449-
dc.identifier.eissn2072-6694-
dc.identifier.pmid38473248-
dc.subject.keywordantivirals-
dc.subject.keywordcancer-
dc.subject.keywordcarcinogenesis-
dc.subject.keywordcomplications-
dc.subject.keywordhepatitis B virus-
dc.subject.keywordliver tumor-
dc.subject.keywordnucleotide analogues-
dc.subject.keywordperformance-
dc.subject.keywordprediction model-
dc.subject.keywordrisk reduction-
dc.contributor.alternativeNameAhn, Sang Hoon-
dc.contributor.affiliatedAuthor안상훈-
dc.citation.volume16-
dc.citation.number5-
dc.citation.startPage887-
dc.identifier.bibliographicCitationCANCERS, Vol.16(5) : 887, 2024-02-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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