Twelve-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

被引:1
|
作者
Tseng, Yu-Ting [1 ]
Yang, Chia-Jui [2 ,3 ]
Kim, Yeon-Sook [4 ]
Choi, Jun Yong [5 ]
Wong, Chen Seong [6 ]
Lee, Kuan-Yeh [7 ]
Lee, Jeong-a [8 ]
Chang, Jack [7 ]
Harrison, Rebecca [9 ]
Marongiu, Andrea [9 ]
Lee, Sun Hee [10 ,11 ]
Hung, Chien-Ching [12 ,13 ,14 ,15 ]
机构
[1] Kaohsiung Vet Gen Hosp, Dept Med, Div Infect Dis, Kaohsiung, Taiwan
[2] Far Eastern Mem Hosp, Dept Internal Med, New Taipei, Taiwan
[3] Natl Yang Ming Chiao Tung Univ, Sch Med, Taipei, Taiwan
[4] Chungnam Natl Univ, Sch Med, Dept Internal Med, Div Infect Dis, Daejeon, South Korea
[5] Yonsei Univ, Coll Med, Dept Internal Med, Div Infect Dis, Seoul, South Korea
[6] Natl Ctr Infect Dis, Dept Infect Dis, Singapore, Singapore
[7] Gilead Sci, Med Affairs, Taipei, Taiwan
[8] Gilead Sci Korea Ltd, Med Affairs, Seoul, South Korea
[9] Gilead Sci Europe Ltd, Real World Evidence, Uxbridge, England
[10] Pusan Natl Univ, Sch Med, Dept Internal Med, Busan, South Korea
[11] Pusan Natl Univ Hosp, Busan, South Korea
[12] Natl Taiwan Univ Hosp, Dept Internal Med, Yunlin Branch, Yunlin, South Korea
[13] Natl Taiwan Univ, Dept Trop Med & Parasitol, Coll Med, Taipei, Taiwan
[14] Natl Taiwan Univ Hosp, Dept Internal Med, Taipei, Taiwan
[15] Natl Taiwan Univ, Coll Med, Taipei, Taiwan
关键词
Antiretroviral therapy; Integrase strand transfer inhibitor; Nucleoside reverse transcriptase inhibitor; Real-world evidence; INFECTION; REGIMENS;
D O I
10.1016/j.jmii.2024.07.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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 <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/).
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页码:760 / 770
页数:11
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