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An expert review on the use of tenofovir alafenamide for the treatment of chronic hepatitis B virus infection in Asia

dc.contributor.authorMichael R. Charltonen_US
dc.contributor.authorAltaf Alamen_US
dc.contributor.authorAkash Shuklaen_US
dc.contributor.authorBekhbold Dashtserenen_US
dc.contributor.authorCosmas Rinaldi Adithya Lesmanaen_US
dc.contributor.authorDavadoorj Dugeren_US
dc.contributor.authorDiana Alcantara Payawalen_US
dc.contributor.authorDo Duy Cuongen_US
dc.contributor.authorGanbolor Jargalsaikhanen_US
dc.contributor.authorIan Homer Yee Cuaen_US
dc.contributor.authorJose Decena Sollanoen_US
dc.contributor.authorKaram Romeo Singhen_US
dc.contributor.authorKaushal Madanen_US
dc.contributor.authorKhin Maung Winen_US
dc.contributor.authorKhin Pyone Kyien_US
dc.contributor.authorKyaw Soe Tunen_US
dc.contributor.authorMohd Salihen_US
dc.contributor.authorMukul Rastogien_US
dc.contributor.authorNeeraj Sarafen_US
dc.contributor.authorPham Thi Thu Thuyen_US
dc.contributor.authorPham Tran Dieu Hienen_US
dc.contributor.authorRino Alvani Ganien_US
dc.contributor.authorRosmawati Mohameden_US
dc.contributor.authorTawesak Tanwandeeen_US
dc.contributor.authorTeerha Piratvisuthen_US
dc.contributor.authorWattana Sukeepaisarnjaroenen_US
dc.contributor.authorWin Naingen_US
dc.contributor.authorZahid Yasin Hashmien_US
dc.contributor.otherMedanta Institute of Digestive & Hepatobiliary Sciencesen_US
dc.contributor.otherFortis Healthcare Ltd.en_US
dc.contributor.otherYangon General Hospitalen_US
dc.contributor.otherMongolian National University of Medical Sciencesen_US
dc.contributor.otherUniversity of Santo Tomas Hospitalen_US
dc.contributor.otherBach Mai Hospitalen_US
dc.contributor.otherUniversity of Indonesia, RSUPN Dr. Cipto Mangunkusumoen_US
dc.contributor.otherThe University of Chicagoen_US
dc.contributor.otherTaipei Medical Universityen_US
dc.contributor.otherKhon Kaen Universityen_US
dc.contributor.otherUniversity of Malaya Medical Centreen_US
dc.contributor.otherFaculty of Medicine, Siriraj Hospital, Mahidol Universityen_US
dc.contributor.otherPrince of Songkla Universityen_US
dc.contributor.otherLokmanya Tilak Municipal Medical Collegeen_US
dc.contributor.otherGI Hepatologyen_US
dc.contributor.otherMyanmar GI and Liver Societyen_US
dc.contributor.otherLiver Foundationen_US
dc.contributor.otherLiver Centeren_US
dc.contributor.otherUniversity of Medicine 1en_US
dc.contributor.otherMax Smart Super Speciality Hospitalen_US
dc.contributor.otherCardinal Santos Medical Centeren_US
dc.contributor.otherSt. Luke's Medical Center-Global Cityen_US
dc.contributor.otherQuaid-e-Azam International Hospitalen_US
dc.contributor.otherDHQ Hospitalen_US
dc.contributor.otherPham Ngoc Thach University of Medicineen_US
dc.contributor.otherRegional Institute of Medical Scienceen_US
dc.date.accessioned2020-08-25T11:30:24Z
dc.date.available2020-08-25T11:30:24Z
dc.date.issued2020-01-01en_US
dc.description.abstract© 2020, The Author(s). Asia has intermediate-to-high prevalence and high morbidity of hepatitis B virus (HBV) infection. The use of guideline-recommended nucleos(t)ide analogs with high barrier to resistance, such as entecavir (ETV), tenofovir disoproxil fumarate (TDF), and tenofovir alafenamide (TAF), is one of the key interventions for curbing HBV infection and associated morbidity in Asia. However, there are some challenges to the use of ETV and TDF; while ETV is associated with high resistance in lamivudine (LAM)-exposed (especially LAM-refractory) patients; bone and renal safety issues are a major concern with TDF. Hence, a panel of twenty-eight expert hepatologists from Asia convened, reviewed the literature, and developed the current expert opinion-based review article for the use of TAF in the resource-constrained settings in Asia. This article provides a comprehensive review of two large, phase 3, double-blind, randomized controlled trials of TAF versus TDF in HBeAg-negative (study 0108) and HBeAg-positive (study 0110) chronic HBV patients (> 70% Asians). These studies revealed as follows: (1) non-inferiority for the proportion of patients who had HBV DNA < 29 IU/mL; (2) significantly high rate of normalization of alanine aminotransferase levels; (3) no incidence of resistance; and (4) significantly better bone and renal safety, with TAF vs. TDF up to 144 weeks. Considering the benefits of TAF, the expert panel proposed recommendations for optimizing the use of TAF in Asia, along with guidance on specific patient groups at risk of renal or bone disease suitable for TAF therapy. The guidance provided in this article may help clinicians optimize the use of TAF in Asia.en_US
dc.identifier.citationJournal of Gastroenterology. (2020)en_US
dc.identifier.doi10.1007/s00535-020-01698-4en_US
dc.identifier.issn14355922en_US
dc.identifier.issn09441174en_US
dc.identifier.other2-s2.0-85087857583en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/58344
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85087857583&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleAn expert review on the use of tenofovir alafenamide for the treatment of chronic hepatitis B virus infection in Asiaen_US
dc.typeReviewen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85087857583&origin=inwarden_US

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