Realizing the Promise of Dolutegravir in Effectively Treating Children and Adolescents Living With HIV in Real-world Settings in 6 Countries in Eastern and Southern Africa

Author:

Bacha Jason Michael123ORCID,Dlamini Sandile24,Anabwani Florence4,Gwimile Judith5,Kanywa Jacqueline Balungi6,Farirai John7,Bvumbwe Menard8,Tsotako Mabene9,Steffy Teresa129,Nguyen Diane1210,Mendez-Reyes Jose Euberto111,Elyanu Peter6,Haq Heather12

Affiliation:

1. Department of Pediatrics, Baylor College of Medicine, Houston, Texas

2. Baylor College of Medicine International Pediatric AIDS Initiative (BIPAI) at Texas Children’s Hospital, Baylor College of Medicine, Houston, Texas

3. Baylor College of Medicine Children’s Foundation - Tanzania, Mbeya, Tanzania

4. Baylor College of Medicine Children’s Foundation - Eswatini, Mbabane, Eswatini

5. Baylor College of Medicine Children’s Foundation - Tanzania, Mwanza, Tanzania

6. Baylor College of Medicine Children’s Foundation - Uganda, Kampala, Uganda

7. Botswana-Baylor Children’s Clinical Centre of Excellence Trust, Gaborone, Botswana

8. Baylor College of Medicine Children’s Foundation - Malawi, Lilongwe, Malawi

9. Baylor College of Medicine Children’s Foundation – Lesotho, Maseru, Lesotho

10. Department of Education, Innovation, and Technology, Baylor College of Medicine, Houston, Texas

11. Texas Children’s Hospital, Houston, Texas.

Abstract

Background: Despite encouraging results from clinical trials and in high-income countries, large-scale data on the effectiveness and safety of dolutegravir (DTG) in children and adolescents living with HIV (CALHIV) are lacking in low- and middle-income countries (LMICs). Methods: Retrospective analysis was performed among CALHIV 0–19 years old and weighing greater than or equal to 20 kg who received DTG from 2017 to 2020 at sites in Botswana, Eswatini, Lesotho, Malawi, Tanzania and Uganda to determine effectiveness, safety and predictors of viral load suppression (VLS) among CALHIV using DTG, including through single drug substitutions (SDS). Results: Among 9419 CALHIV using DTG, 7898 had a documented post-DTG VL, and VLS post-DTG was 93.4% (7378/7898). VLS for antiretroviral therapy (ART) initiations was 92.4% (246/263), and VLS was maintained for the ART-experienced [92.9% (7026/7560) pre- vs. 93.5% (7071/7560) post-DTG; P = 0.14). Among previously unsuppressed, 79.8% (426/534) achieved VLS with DTG. Only 5 patients reported a Grade 3 or 4 adverse event (0.057 per 100 patient-years) requiring DTG discontinuation. History of protease inhibitor-based ART [odds ratio (OR) = 1.53; 95% confidence interval (CI): 1.16–2.03], care in Tanzania (OR = 5.45; 95% CI: 3.41–8.70), and being 15–19 years old (OR = 1.31; 95% CI: 1.03–1.65) were associated with gain of VLS post-DTG. Predictors of VLS on DTG included VLS before DTG (OR = 3.87; 95% CI: 3.03–4.95) and using the once-daily, single tab tenofovir-lamivudine-DTG regimen (OR = 1.78; 95% CI: 1.43–2.22). SDS maintained VLS [95.9% (2032/2120) pre- vs. 95.0% (2014/2120) post-SDS with DTG; P = 0.19], and 83.0% (73/88) of unsuppressed gained VLS using SDS with DTG. Conclusions: We found DTG to be highly effective and safe within our cohort of CALHIV in LMICs. These findings can empower clinicians to prescribe DTG confidently to eligible CALHIV.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Infectious Diseases,Microbiology (medical),Pediatrics, Perinatology and Child Health

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