{"title":"Long-acting Injectable Antiretroviral Therapy in South African Adolescents and Young Adults - Week 48 results from the AFINAty Study.","authors":"Chantel Schreuder, Nyiko Mashele, Rufaro Mvududu, Millicent Atujuna, Linda-Gail Bekker, Catherine Orrell, Lauren Jennings","doi":"10.1097/QAI.0000000000003973","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Long-acting injectable antiretroviral therapy (LAI-ART) with cabotegravir and rilpivirine offers a promising alternative to daily oral ART, particularly for young people living with HIV (YLHIV). However, there are limited data on the feasibility, acceptability and efficacy of LAI-ART delivery in lower- and middle-income countries.</p><p><strong>Methods: </strong>We conducted a 48-week, community-based study of cabotegravir and rilpivirine LAI-ART among YLHIV aged 12-24 years in Cape Town, South Africa. Participants (virally suppressed, struggling with adherence or ART naïve) were required to be virally suppressed (<50 copies/ml) on first-line ART at the end of the screening phase before switching to cabotegravir and rilpivirine LAI-ART every 8 weeks for 48 weeks. Feasibility, retention, adherence to injection schedules, viral suppression and safety were assessed. Virological failure was defined as two consecutive viral loads ≥200 copies/ml.</p><p><strong>Results: </strong>Between December 2022 and December 2023, 172 participants were screened and 134 (77·9%) switched to LAI-ART. The median age was 20 years and 62·7% were assigned female at birth. Nearly one quarter (23·1%) were under 18 years of age. Overall, 47% had prior NNRTI exposure. Retention at week 48 was 98·5% with 97·5% of all injections given on schedule. Viral suppression, as indicated by VL <50 copies/ml, at week 48 was achieved by 95·5% with no confirmed virological failures. All participants who completed week 48 opted to remain on LAI-ART.</p><p><strong>Interpretation: </strong>LAI-ART was safe, highly acceptable and effective among YLHIV. These findings support the feasibility of implementing LAI-ART through community-based models in sub-Saharan Africa.</p>","PeriodicalId":520658,"journal":{"name":"Journal of acquired immune deficiency syndromes (1999)","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2026-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of acquired immune deficiency syndromes (1999)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1097/QAI.0000000000003973","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Long-acting injectable antiretroviral therapy (LAI-ART) with cabotegravir and rilpivirine offers a promising alternative to daily oral ART, particularly for young people living with HIV (YLHIV). However, there are limited data on the feasibility, acceptability and efficacy of LAI-ART delivery in lower- and middle-income countries.
Methods: We conducted a 48-week, community-based study of cabotegravir and rilpivirine LAI-ART among YLHIV aged 12-24 years in Cape Town, South Africa. Participants (virally suppressed, struggling with adherence or ART naïve) were required to be virally suppressed (<50 copies/ml) on first-line ART at the end of the screening phase before switching to cabotegravir and rilpivirine LAI-ART every 8 weeks for 48 weeks. Feasibility, retention, adherence to injection schedules, viral suppression and safety were assessed. Virological failure was defined as two consecutive viral loads ≥200 copies/ml.
Results: Between December 2022 and December 2023, 172 participants were screened and 134 (77·9%) switched to LAI-ART. The median age was 20 years and 62·7% were assigned female at birth. Nearly one quarter (23·1%) were under 18 years of age. Overall, 47% had prior NNRTI exposure. Retention at week 48 was 98·5% with 97·5% of all injections given on schedule. Viral suppression, as indicated by VL <50 copies/ml, at week 48 was achieved by 95·5% with no confirmed virological failures. All participants who completed week 48 opted to remain on LAI-ART.
Interpretation: LAI-ART was safe, highly acceptable and effective among YLHIV. These findings support the feasibility of implementing LAI-ART through community-based models in sub-Saharan Africa.