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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

Authors
 Tseng, Yu-Ting  ;  Yang, Chia-Jui  ;  Kim, Yeon-Sook  ;  Choi, Jun Yong  ;  Wong, Chen Seong  ;  Lee, Kuan-Yeh  ;  Lee, Jeong-a  ;  Chang, Jack  ;  Harrison, Rebecca  ;  Marongiu, Andrea  ;  Lee, Sun Hee  ;  Hung, Chien-Ching 
Citation
 JOURNAL OF MICROBIOLOGY IMMUNOLOGY AND INFECTION, Vol.57(5) : 760-770, 2024-10 
Journal Title
JOURNAL OF MICROBIOLOGY IMMUNOLOGY AND INFECTION
ISSN
 1684-1182 
Issue Date
2024-10
Keywords
Antiretroviral therapy ; Integrase strand transfer inhibitor ; Nucleoside reverse transcriptase inhibitor ; Real-world evidence
Abstract
Background: 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 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/).
DOI
10.1016/j.jmii.2024.07.003
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Choi, Jun Yong(최준용) ORCID logo https://orcid.org/0000-0002-2775-3315
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/200979
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