Viro-Immunological Efficacy and Safety of Bictegravir/Emtricitabine/Tenofovir Alafenamide among Women Living with HIV: A 96-Week Post-Switch Analysis from the Real-Life SHiNe-SHiC Cohort

<b>Background/Objectives</b>: Out of 39.9 million adults living with HIV in 2022, 20 million were women. Despite bearing a significant burden, women remain underrepresented in clinical trials, including those for antiretroviral treatments (ART). This study evaluates the safety and efficacy of the bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF) regimen in a real-life cohort of 99 women with HIV (females with HIV, FWH) over 48 and 96 weeks. <b>Methods</b>: A retrospective cohort study utilized data from the Sardinian HIV Network and Sicilian HIV Cohort (SHiNe-SHiC) research group. The study included FWH, who started B/F/TAF as a treatment switch. The primary objectives were achieving and maintaining an HIV RNA level of <50 copies/mL at 48 and 96 weeks. Secondary objectives included treatment safety, durability, and reasons for discontinuation. Data on demographics, viro-immunological markers, lipid profiles, and treatment interruptions were extracted for analysis. <b>Results</b>: Among the 99 FWH, the median age was 51.9 years, and the median duration of HIV was 15.1 years. At baseline, 80.8% had undetectable HIV-RNA, which increased to 93.8% at 96 weeks. There was a statistically significant increase in CD4 cells/mL (48w <i>p</i> < 0.001, 96w <i>p</i> < 0.001) and CD4/CD8 ratio (48w <i>p</i> < 0.009, 96w <i>p</i> < 0.048), and reductions in total cholesterol (48w <i>p</i> < 0.003, 96w <i>p</i> < 0.006) and LDL (48w <i>p</i> < 0.004, 96w <i>p</i> < 0.009) levels at 48 and 96 weeks. Nine treatment interruptions were noted, with one due to adverse events. The regimen was well-tolerated overall. <b>Conclusions</b>: B/F/TAF demonstrated high efficacy and safety in this real-world cohort of FWH, highlighting the critical need for gender-focused research in HIV treatment. Ensuring equitable access to effective treatment options for women is imperative for the global health community's efforts to eliminate HIV.

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Publication Details

Journal
Biomedicines
Published
2024-10-11
DOI
https://doi.org/10.3390/biomedicines12102311
Citations
3
Primary Topic
HIV/AIDS drug development and treatment
Type
article
Field-Weighted Citation Impact
1.17
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article

Viro-Immunological Efficacy and Safety of Bictegravir/Emtricitabine/Tenofovir Alafenamide among Women Living with HIV: A 96-Week Post-Switch Analysis from the Real-Life SHiNe-SHiC Cohort

Manuela Ceccarelli, Andrea De Vito, Giulia Moi, Goffredo Angioni et al.
3 citations
Biomedicines
HIV/AIDS drug development and treatment
1.17
article

Viro-Immunological Efficacy and Safety of Bictegravir/Emtricitabine/Tenofovir Alafenamide among Women Living with HIV: A 96-Week Post-Switch Analysis from the Real-Life SHiNe-SHiC Cohort

Manuela Ceccarelli, Andrea De Vito, Giulia Moi, Goffredo Angioni, Emmanuele Venanzi Rullo, Benedetto Maurizio Celesia, Agnese Colpani, Antonio Albanese, Arturo Montineri, Grazia Pantò, Giuseppe Nunnari, Carmelo Iacobello, Giordano Madeddu, Andrea Marıno, Bruno Cacopardo, G. Conti, Giovanni Francesco Pellicanò, Serena Spampinato, C. Frascà, Sonia Sofia
article en
3 citations

Abstract

<b>Background/Objectives</b>: Out of 39.9 million adults living with HIV in 2022, 20 million were women. Despite bearing a significant burden, women remain underrepresented in clinical trials, including those for antiretroviral treatments (ART). This study evaluates the safety and efficacy of the bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF) regimen in a real-life cohort of 99 women with HIV (females with HIV, FWH) over 48 and 96 weeks. <b>Methods</b>: A retrospective cohort study utilized data from the Sardinian HIV Network and Sicilian HIV Cohort (SHiNe-SHiC) research group. The study included FWH, who started B/F/TAF as a treatment switch. The primary objectives were achieving and maintaining an HIV RNA level of <50 copies/mL at 48 and 96 weeks. Secondary objectives included treatment safety, durability, and reasons for discontinuation. Data on demographics, viro-immunological markers, lipid profiles, and treatment interruptions were extracted for analysis. <b>Results</b>: Among the 99 FWH, the median age was 51.9 years, and the median duration of HIV was 15.1 years. At baseline, 80.8% had undetectable HIV-RNA, which increased to 93.8% at 96 weeks. There was a statistically significant increase in CD4 cells/mL (48w <i>p</i> < 0.001, 96w <i>p</i> < 0.001) and CD4/CD8 ratio (48w <i>p</i> < 0.009, 96w <i>p</i> < 0.048), and reductions in total cholesterol (48w <i>p</i> < 0.003, 96w <i>p</i> < 0.006) and LDL (48w <i>p</i> < 0.004, 96w <i>p</i> < 0.009) levels at 48 and 96 weeks. Nine treatment interruptions were noted, with one due to adverse events. The regimen was well-tolerated overall. <b>Conclusions</b>: B/F/TAF demonstrated high efficacy and safety in this real-world cohort of FWH, highlighting the critical need for gender-focused research in HIV treatment. Ensuring equitable access to effective treatment options for women is imperative for the global health community's efforts to eliminate HIV.

BiomedicinesVol. 12(10)
University of Messina (IT), University of Sassari (IT), Università degli Studi di Enna Kore (IT), University of Catania (IT), Ospedale Garibaldi (IT), Santissima Trinità (IT), Ospedale Cannizzaro (IT), Azienda Ospedaliera Ospedali Riuniti Papardo Piemonte (IT)
Openalex Percentile: Top 21%
HIV/AIDS drug development and treatment
1.17
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