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Twelve-month effectiveness and safety of bictegravir/emtricitabine/tenofovir alafenamide in treatment-naıve and treatment-experienced people with HIV: Findings from the Asia cohort of the BICSTaR study

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dc.contributor.authorTseng, Yu-Ting-
dc.contributor.authorYang, Chia-Jui-
dc.contributor.authorKim, Yeon-Sook-
dc.contributor.authorChoi, Jun Yong-
dc.contributor.authorWong, Chen Seong-
dc.contributor.authorLee, Kuan-Yeh-
dc.contributor.authorLee, Jeong-a-
dc.contributor.authorChang, Jack-
dc.contributor.authorHarrison, Rebecca-
dc.contributor.authorMarongiu, Andrea-
dc.contributor.authorLee, Sun Hee-
dc.contributor.authorHung, Chien-Ching-
dc.date.accessioned2024-12-06T03:04:51Z-
dc.date.available2024-12-06T03:04:51Z-
dc.date.created2025-06-25-
dc.date.issued2024-10-
dc.identifier.issn1684-1182-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/200979-
dc.description.abstractBackground: The ongoing, observational BICSTaR (BICtegravir Single Tablet Regimen) cohort study is evaluating real-world effectiveness and safety of bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF) in people with HIV across 14 countries over 24 months. We present 12-month data from the BICSTaR Asia cohort. Methods: Data were pooled from retrospective and prospective cohorts of antiretroviral therapy (ART)-na & imath;ve (hereafter, TN) and ART-experienced (hereafter, TE) people with HIV (aged >= 21 years) receiving B/F/TAF in routine clinical care in the Republic of Korea, Singapore, and Taiwan. Analyses included effectiveness (primary endpoint: HIV-1 RNA <50 copies/ml, missing Z excluded analysis), CD4 count, CD4/CD8 ratio, safety, treatment persistence, and patient-reported outcomes (prospective group). Results: The analysis population included 328 participants (80 retrospective, 248 prospective; 65 TN, 263 TE). Participants were predominantly male (96.9% TN, 93.2% TE) with >= 1 comorbidity (52.3% TN, 57.8% TE); median age (years) was 31 (TN) and 42 (TE). Following 12 months of B/F/TAF, HIV-1 RNA was <50 copies/ml in 98.2% (54/55) of TN and 97.0% (227/234) of TE participants. Median (Q1, Q3) CD4 cell count increased by +187 (119, 291) cells/ml in the TN group (p < 0.001) and remained stable (+8 [-91, 110] cells/ml) in the TE group. B/F/TAF persistence was high in the prospective group, with 1/34 (2.9%) TN and 5/214 (2.3%) TE participants discontinuing treatment within 12 months. Drug-related adverse events occurred in 5.8% (19/328) of participants, leading to treatment discontinuation in 0.6% (2/328). Conclusions: Real-world evidence from BICSTaR supports the effectiveness, safety and tolerability of B/F/TAF in people with HIV in Asia. Copyright <feminine ordinal indicator> 2024, Taiwan Society of Microbiology. Published by Elsevier Taiwan LLC. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/bync-nd/4.0/).-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish, Chinese-
dc.publisherElsevier for the Taiwan Society of Microbiology-
dc.relation.isPartOfJOURNAL OF MICROBIOLOGY IMMUNOLOGY AND INFECTION-
dc.relation.isPartOfJOURNAL OF MICROBIOLOGY IMMUNOLOGY AND INFECTION-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleTwelve-month effectiveness and safety of bictegravir/emtricitabine/tenofovir alafenamide in treatment-naı<spacing diaeresis>ve and treatment-experienced people with HIV: Findings from the Asia cohort of the BICSTaR study-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorTseng, Yu-Ting-
dc.contributor.googleauthorYang, Chia-Jui-
dc.contributor.googleauthorKim, Yeon-Sook-
dc.contributor.googleauthorChoi, Jun Yong-
dc.contributor.googleauthorWong, Chen Seong-
dc.contributor.googleauthorLee, Kuan-Yeh-
dc.contributor.googleauthorLee, Jeong-a-
dc.contributor.googleauthorChang, Jack-
dc.contributor.googleauthorHarrison, Rebecca-
dc.contributor.googleauthorMarongiu, Andrea-
dc.contributor.googleauthorLee, Sun Hee-
dc.contributor.googleauthorHung, Chien-Ching-
dc.identifier.doi10.1016/j.jmii.2024.07.003-
dc.relation.journalcodeJ01595-
dc.identifier.eissn1995-9133-
dc.identifier.pmid39079772-
dc.subject.keywordAntiretroviral therapy-
dc.subject.keywordIntegrase strand transfer inhibitor-
dc.subject.keywordNucleoside reverse transcriptase inhibitor-
dc.subject.keywordReal-world evidence-
dc.contributor.alternativeNameChoi, Jun Yong-
dc.contributor.affiliatedAuthorChoi, Jun Yong-
dc.identifier.scopusid2-s2.0-85199986014-
dc.identifier.wosid001320666400001-
dc.citation.volume57-
dc.citation.number5-
dc.citation.startPage760-
dc.citation.endPage770-
dc.identifier.bibliographicCitationJOURNAL OF MICROBIOLOGY IMMUNOLOGY AND INFECTION, Vol.57(5) : 760-770, 2024-10-
dc.identifier.rimsid87002-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordAuthorAntiretroviral therapy-
dc.subject.keywordAuthorIntegrase strand transfer inhibitor-
dc.subject.keywordAuthorNucleoside reverse transcriptase inhibitor-
dc.subject.keywordAuthorReal-world evidence-
dc.subject.keywordPlusINFECTION-
dc.subject.keywordPlusREGIMENS-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.relation.journalWebOfScienceCategoryInfectious Diseases-
dc.relation.journalWebOfScienceCategoryMicrobiology-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalResearchAreaInfectious Diseases-
dc.relation.journalResearchAreaMicrobiology-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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