Roberta Gagliardini , Marta Camici , Simone Lanini , Rita Bellagamba , Sandrine Ottou , Maria Maddalena Plazzi , Alessandra Vergori , Valentina Mazzotta , Annalisa Mondi , Marisa Fusto , Jessica Paulicelli , Massimo Tempestilli , Carmela Pinnetti , Elisabetta Grilli , Ilaria Mastrorosa , Federico De Zottis , Giulia Del Duca , Andrea Antinori
{"title":"病毒学抑制的HIV感染者从依非韦伦/恩曲他滨/替诺福韦二氧吡酯(EFV/FTC/TDF)改用比替格拉韦/恩曲他滨/替诺福韦丙烯胺(B/F/TAF):来自一项非随机临床试验(EBONY研究)的结果。","authors":"Roberta Gagliardini , Marta Camici , Simone Lanini , Rita Bellagamba , Sandrine Ottou , Maria Maddalena Plazzi , Alessandra Vergori , Valentina Mazzotta , Annalisa Mondi , Marisa Fusto , Jessica Paulicelli , Massimo Tempestilli , Carmela Pinnetti , Elisabetta Grilli , Ilaria Mastrorosa , Federico De Zottis , Giulia Del Duca , Andrea Antinori","doi":"10.1016/j.ijid.2025.107961","DOIUrl":null,"url":null,"abstract":"<div><h3>Objectives</h3><div>No previous studies specifically explored the switch from efavirenz to bictegravir (BIC)-containing three-drug antiretroviral regimens. This study aimed to evaluate the efficacy and safety outcomes of a treatment switch from efavirenz/emtricitabine/tenofovir disoproxil fumarate (EFV/FTC/TDF) given once daily (OD) or on alternate days (ATAD) to BIC/emtricitabine/tenofovir alafenamide (BIC/FTC/TAF) in virologically suppressed people with HIV (PWH).</div></div><div><h3>Methods</h3><div>A pilot, single-arm, prospective study was conducted.</div></div><div><h3>Results</h3><div>Overall, 234 PWH were enrolled. 217 of 234 (92.7%, 95% confidence interval [CI], 88.6-95.7%) participants had HIV-RNA <40 cp/ml at 48 weeks. Virological failure occurred in three participants, none with documented resistance, and all resuppressed without antiretroviral therapy change. After 48 weeks, a slight increase in cluster of differentiation (CD)4 cell count was observed from the baseline (+ 59 cells/mmc, 95% CI, 31; 86, <em>P</em> <0.001), but not in CD4/CD8 ratio. A slight increase in creatinine (mean change +0.11 mg/dl, 95% CI 0.10; 0.13, <em>P</em> <0.001) and a decrease in total cholesterol (mean change −8 mg/dl, 95% CI −14; −3, <em>P</em> = 0.001) were also observed.</div></div><div><h3>Conclusions</h3><div>Our data showed that BIC/FTC/TAF demonstrated high virologic and immunologic efficacy and an excellent safety profile.</div></div>","PeriodicalId":14006,"journal":{"name":"International Journal of Infectious Diseases","volume":"158 ","pages":"Article 107961"},"PeriodicalIF":4.3000,"publicationDate":"2025-06-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Switching to bictegravir/emtricitabine/tenofovir alafenamide from efavirenz/emtricitabine/tenofovir disoproxil in virologically suppressed people with HIV: findings from a non-randomized clinical trial (EBONY study)\",\"authors\":\"Roberta Gagliardini , Marta Camici , Simone Lanini , Rita Bellagamba , Sandrine Ottou , Maria Maddalena Plazzi , Alessandra Vergori , Valentina Mazzotta , Annalisa Mondi , Marisa Fusto , Jessica Paulicelli , Massimo Tempestilli , Carmela Pinnetti , Elisabetta Grilli , Ilaria Mastrorosa , Federico De Zottis , Giulia Del Duca , Andrea Antinori\",\"doi\":\"10.1016/j.ijid.2025.107961\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objectives</h3><div>No previous studies specifically explored the switch from efavirenz to bictegravir (BIC)-containing three-drug antiretroviral regimens. This study aimed to evaluate the efficacy and safety outcomes of a treatment switch from efavirenz/emtricitabine/tenofovir disoproxil fumarate (EFV/FTC/TDF) given once daily (OD) or on alternate days (ATAD) to BIC/emtricitabine/tenofovir alafenamide (BIC/FTC/TAF) in virologically suppressed people with HIV (PWH).</div></div><div><h3>Methods</h3><div>A pilot, single-arm, prospective study was conducted.</div></div><div><h3>Results</h3><div>Overall, 234 PWH were enrolled. 217 of 234 (92.7%, 95% confidence interval [CI], 88.6-95.7%) participants had HIV-RNA <40 cp/ml at 48 weeks. Virological failure occurred in three participants, none with documented resistance, and all resuppressed without antiretroviral therapy change. After 48 weeks, a slight increase in cluster of differentiation (CD)4 cell count was observed from the baseline (+ 59 cells/mmc, 95% CI, 31; 86, <em>P</em> <0.001), but not in CD4/CD8 ratio. A slight increase in creatinine (mean change +0.11 mg/dl, 95% CI 0.10; 0.13, <em>P</em> <0.001) and a decrease in total cholesterol (mean change −8 mg/dl, 95% CI −14; −3, <em>P</em> = 0.001) were also observed.</div></div><div><h3>Conclusions</h3><div>Our data showed that BIC/FTC/TAF demonstrated high virologic and immunologic efficacy and an excellent safety profile.</div></div>\",\"PeriodicalId\":14006,\"journal\":{\"name\":\"International Journal of Infectious Diseases\",\"volume\":\"158 \",\"pages\":\"Article 107961\"},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2025-06-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Infectious Diseases\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1201971225001857\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"INFECTIOUS DISEASES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Infectious Diseases","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1201971225001857","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
Switching to bictegravir/emtricitabine/tenofovir alafenamide from efavirenz/emtricitabine/tenofovir disoproxil in virologically suppressed people with HIV: findings from a non-randomized clinical trial (EBONY study)
Objectives
No previous studies specifically explored the switch from efavirenz to bictegravir (BIC)-containing three-drug antiretroviral regimens. This study aimed to evaluate the efficacy and safety outcomes of a treatment switch from efavirenz/emtricitabine/tenofovir disoproxil fumarate (EFV/FTC/TDF) given once daily (OD) or on alternate days (ATAD) to BIC/emtricitabine/tenofovir alafenamide (BIC/FTC/TAF) in virologically suppressed people with HIV (PWH).
Methods
A pilot, single-arm, prospective study was conducted.
Results
Overall, 234 PWH were enrolled. 217 of 234 (92.7%, 95% confidence interval [CI], 88.6-95.7%) participants had HIV-RNA <40 cp/ml at 48 weeks. Virological failure occurred in three participants, none with documented resistance, and all resuppressed without antiretroviral therapy change. After 48 weeks, a slight increase in cluster of differentiation (CD)4 cell count was observed from the baseline (+ 59 cells/mmc, 95% CI, 31; 86, P <0.001), but not in CD4/CD8 ratio. A slight increase in creatinine (mean change +0.11 mg/dl, 95% CI 0.10; 0.13, P <0.001) and a decrease in total cholesterol (mean change −8 mg/dl, 95% CI −14; −3, P = 0.001) were also observed.
Conclusions
Our data showed that BIC/FTC/TAF demonstrated high virologic and immunologic efficacy and an excellent safety profile.
期刊介绍:
International Journal of Infectious Diseases (IJID)
Publisher: International Society for Infectious Diseases
Publication Frequency: Monthly
Type: Peer-reviewed, Open Access
Scope:
Publishes original clinical and laboratory-based research.
Reports clinical trials, reviews, and some case reports.
Focuses on epidemiology, clinical diagnosis, treatment, and control of infectious diseases.
Emphasizes diseases common in under-resourced countries.