Viral Suppression, Viral Failure, and Safety Outcomes in Children and Adolescents With HIV on Dolutegravir in Europe and Thailand

Karen Scott*, John O'Rourke, Charlotte Jackson, Luminita Ene, Luisa Galli, Tessa Goetghebuer, Cassidy Henegar, Christoph Königs, Magdalena Marczyńska, Lars Naver, Antoni Noguera-Julian, Paolo Paioni, Jose T Ramos, Birgitte Smith, Wipaporn Natalie Songtaweesin, Vana Spoulou, Nattakarn Tantawarak, Anna Turkova, Vani Vannappagari, Alla VolokhaAlastair Bamford, Hannah Castro, Elizabeth Chappell, Giorgia Dalla Valle, Caroline Foster, Sara Guillén Martín, Luis Manuel Prieto Tato, Thanyawee Puthanakit, Halyna Sherstiuk, Irina Shkurka, Sandra Soeria-Atmadja, Ali Judd, Siobhan Crichton, Intira Jeannie Collins

*Corresponding author af dette arbejde

Abstract

BACKGROUND: Dolutegravir (DTG) is a preferred anchor antiretroviral therapy (ART) for children and adolescents with HIV (CAWH).

METHODS: We assessed the effectiveness and safety of DTG in CAWH aged 0-18 years at DTG start in routine care in Europe and Thailand, evaluating viral suppression (viral load [VL] <50 copies/mL), cumulative incidence and associated factors of viral failure (VF; confirmed VL ≥400 copies/mL) and safety outcomes.

RESULTS: Of 1230 CAWH on DTG, 49% were female. At DTG start, median (IQR) age was 14 (11-16) years, 10% were ART-naive, 49% ART-experienced/suppressed (VL <200 copies/mL), 13% ART-experienced/viremic (VL ≥200 copies/mL), and 28% ART-experienced/unknown VL. Median duration on DTG was 93 (49-163) weeks. Virall suppression was 88%-91% throughout follow-up. Cumulative incidence (95% CI) of VF at weeks 96 and 144 was 4.3% (3.1%-6.1%) and 8.3% (6.2%-11.1%). Increased risk of VF was associated with female sex, ART-experienced/viremic, advanced/severe immunosuppression, previous treatment failure, and region (P < .05, adjusting for age, sex and ART/VL status). The risk of VF was lower on DTG than CAWH on protease-inhibitor-based regimens (P < .001). Among 1146 with clinical data, 26 (2%) experienced 52 DTG-related adverse events, including 5 serious adverse events. Of 849 with laboratory data, 44 (5%) had 54 grade ≥3 events (<1 per 100 person-years). DTG discontinuation by weeks 96 and 144 was 5.0% (3.8%-6.7%) and 9.5% (7.5%-12.0%).

CONCLUSIONS: DTG was well tolerated, with ∼90% virally suppressed <50 copies/mL. VF was low overall but was significantly higher in children/adolescents ART-experienced and viraemic at DTG start, requiring close monitoring.

OriginalsprogEngelsk
TidsskriftClinical infectious diseases : an official publication of the Infectious Diseases Society of America
Vol/bind81
Udgave nummer4
Sider (fra-til)e115-e127
ISSN1058-4838
DOI
StatusUdgivet - 6 nov. 2025

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