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Safety and effectiveness of switching to Abacavir/Lamivudine plus rilpivirine for maintenance therapy in virologically suppressed HIV-1 individuals in Singapore (SEALS).
Lim, Z C; Hoo, G S; Ang, J H; Teng, C B; Ang, L W; Lee, C C; Leo, Y S; Law, H L; Ng, O T; Wong, C S.
Afiliación
  • Lim ZC; Department of Pharmacy, Ng Teng Fong General Hospital, Singapore, Singapore.
  • Hoo GS; Department of Pharmacy, National Centre of Infectious Diseases, Singapore, Singapore. grace_sr_hoo@ttsh.com.sg.
  • Ang JH; Department of Pharmacy, Tan Tock Seng Hospital, Singapore, Singapore. grace_sr_hoo@ttsh.com.sg.
  • Teng CB; Department of Pharmacy, Tan Tock Seng Hospital, Singapore, Singapore.
  • Ang LW; Department of Pharmacy, Tan Tock Seng Hospital, Singapore, Singapore.
  • Lee CC; Department of Pharmacy, National University of Singapore, Singapore, Singapore.
  • Leo YS; National Public Health and Epidemiology Unit, National Centre for Infectious Diseases, Singapore, Singapore.
  • Law HL; National Centre for Infectious Diseases, Singapore, Singapore.
  • Ng OT; Department of Infectious Diseases, Tan Tock Seng Hospital, Singapore, Singapore.
  • Wong CS; Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
AIDS Res Ther ; 18(1): 80, 2021 11 01.
Article en En | MEDLINE | ID: mdl-34724931
ABSTRACT

BACKGROUND:

The efficacy and tolerability of an antiretroviral regimen are important considerations for selection of HIV-1 infection maintenance therapy. Abacavir/lamivudine plus rilpivirine (ABC/3TC + RPV) has been shown in international studies to be effective and well-tolerated in virologically suppressed individuals. This study evaluated the effectiveness and safety of switching to ABC/3TC + RPV as maintenance therapy in virologically suppressed HIV-1 infected individuals in Singapore.

METHODS:

In this retrospective, single-centre study, we included individuals who were prescribed ABC/3TC + RPV, had HIV-1 viral load (VL) < 50 copies/ml immediately pre-switch, and had no documented history of resistance mutations or virologic failure to any of the components. The follow-up period was 48 ± 12 weeks. The primary outcome was the proportion of individuals who maintained virologic suppression of HIV-1 VL < 50 copies/ml at the end of follow-up period based on on-treatment analysis. The secondary outcomes were the resistance profiles associated with virologic failure, changes in immunologic and metabolic parameters, and the safety profile of ABC/3TC + RPV.

RESULTS:

A total of 222 individuals were included in the study. The primary outcome was achieved in 197 individuals [88.8%, 95% confidence interval 83.7-92.4%]. There were 21 individuals (9.5%) who discontinued treatment for non-virologic reasons. The remaining 4 individuals experienced virologic failure, of whom, 3 of these individuals had developed emergent antiretroviral resistance and had HIV-1 VL > 500 copies/ml at the end of the 48 ± 12 weeks follow-up period. The remaining individual experienced sustained low level viremia and subsequently achieved viral suppression without undergoing resistance testing. A total of 49 adverse events were observed in 31 out of 222 individuals (14.0%), which led to 13 individuals discontinuing therapy. Neuropsychiatric adverse events were most commonly observed (53.1%). A statistically significant increase in CD4 was observed (p < 0.01), with a median absolute change of 31 cells/uL (interquartile range - 31.50 to 140.75). No significant changes in lipid profiles were detected.

CONCLUSION:

ABC/3TC + RPV is a safe and effective switch option for maintenance therapy in virologically suppressed HIV-1 individuals with in Singapore.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Infecciones por VIH / VIH-1 / Lamivudine / Fármacos Anti-VIH Tipo de estudio: Observational_studies Límite: Humans País/Región como asunto: Asia Idioma: En Revista: AIDS Res Ther Año: 2021 Tipo del documento: Article País de afiliación: Singapur

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Infecciones por VIH / VIH-1 / Lamivudine / Fármacos Anti-VIH Tipo de estudio: Observational_studies Límite: Humans País/Región como asunto: Asia Idioma: En Revista: AIDS Res Ther Año: 2021 Tipo del documento: Article País de afiliación: Singapur