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dc.contributor.author문영철*
dc.date.accessioned2023-11-20T16:34:42Z-
dc.date.available2023-11-20T16:34:42Z-
dc.date.issued2023*
dc.identifier.issn2927-9270*
dc.identifier.otherOAK-33929*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/266511-
dc.description.abstractINTRODUCTION:This prospective study aimed to investigate the efficacy and safety of preemptive antiviral therapy with tenofovir disoproxil fumarate (TDF) for HBsAg-positive patients with newly diagnosed diffuse large B-cell lymphoma receiving rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) chemotherapy.METHODS:We enrolled 73 patients from 20 institutions. The primary end point was the absolute risk of hepatitis B virus (HBV)-related hepatitis during preemptive TDF therapy and for 24 weeks after withdrawal from TDF. Hepatitis was defined as a more than 3-fold increase in serum alanine aminotransferase from baseline or an alanine aminotransferase level of ≥100 U/L. HBV-related hepatitis was defined as hepatitis with an increase in serum HBV-DNA to >10 times that of the pre-exacerbation baseline or an absolute increase of ≥20,000 IU/mL compared with the baseline.RESULTS:No patient developed HBV reactivation or HBV-related hepatitis during preemptive antiviral therapy (until 48 weeks after completion of R-CHOP chemotherapy) with TDF. All adverse events were grade 1 or 2. HBV reactivation was reported in 17 (23.3%) patients. All HBV reactivation was developed at a median of 90 days after withdrawal from TDF (range, 37-214 days). Six (8.2%) patients developed HBV-related hepatitis at a median of 88 days after withdrawal from TDF (range, 37-183 days).DISCUSSION:Preemptive TDF therapy in HBsAg-positive patients with diffuse large B-cell lymphoma receiving R-CHOP chemotherapy was safe and effective for preventing HBV-related hepatitis. However, a long-term maintenance strategy of preemptive TDF therapy should be recommended because of the relatively high rate of HBV-related hepatitis after withdrawal from TDF (ClinicalTrials.gov ID: NCT02354846). © 2023 Wolters Kluwer Health. All rights reserved.*
dc.languageEnglish*
dc.publisherWolters Kluwer Health*
dc.subjectantiviral therapy*
dc.subjectdiffuse large B-cell lymphoma*
dc.subjecthepatitis B virus*
dc.subjecttenofovir disoproxil fumarate*
dc.titleA Prospective Study of Preemptive Tenofovir Disoproxil Fumarate Therapy in HBsAg-Positive Patients with Diffuse Large B-Cell Lymphoma Receiving Rituximab Plus Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone*
dc.typeArticle*
dc.relation.issue8*
dc.relation.volume118*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage1373*
dc.relation.lastpage1380*
dc.relation.journaltitleAmerican Journal of Gastroenterology*
dc.identifier.doi10.14309/ajg.0000000000002185*
dc.identifier.wosidWOS:001048672500017*
dc.identifier.scopusid2-s2.0-85166442279*
dc.author.googleKim D.Y.*
dc.author.googleKim Y.R.*
dc.author.googleSuh C.*
dc.author.googleYoon D.H.*
dc.author.googleYang D.-H.*
dc.author.googlePark Y.*
dc.author.googleEom H.S.*
dc.author.googleLee J.-O.*
dc.author.googleKwak J.-Y.*
dc.author.googleKang H.J.*
dc.author.googleHyun S.Y.*
dc.author.googleJo J.-C.*
dc.author.googleChang M.H.*
dc.author.googleYoo K.H.*
dc.author.googleLim S.-N.*
dc.author.googleShin H.-J.*
dc.author.googleKim W.S.*
dc.author.googleKim I.-H.*
dc.author.googleKim M.K.*
dc.author.googleKim H.J.*
dc.author.googleLee W.-S.*
dc.author.googleMun Y.-C.*
dc.author.googleKim J.S.*
dc.contributor.scopusid문영철(7003363716)*
dc.date.modifydate20240422115947*
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