Please use this identifier to cite or link to this item: https://doi.org/10.1186/s12981-021-00402-7
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dc.titleSafety and effectiveness of switching to Abacavir/Lamivudine plus rilpivirine for maintenance therapy in virologically suppressed HIV-1 individuals in Singapore (SEALS)
dc.contributor.authorLim, Z. C.
dc.contributor.authorHoo, G. S.
dc.contributor.authorAng, J. H.
dc.contributor.authorTeng, C. B.
dc.contributor.authorAng, L. W.
dc.contributor.authorLee, C. C.
dc.contributor.authorLeo, Y. S.
dc.contributor.authorLaw, H. L.
dc.contributor.authorNg, O. T.
dc.contributor.authorWong, C. S.
dc.date.accessioned2022-10-13T01:05:14Z
dc.date.available2022-10-13T01:05:14Z
dc.date.issued2021-11-01
dc.identifier.citationLim, 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. (2021-11-01). Safety and effectiveness of switching to Abacavir/Lamivudine plus rilpivirine for maintenance therapy in virologically suppressed HIV-1 individuals in Singapore (SEALS). AIDS Research and Therapy 18 (1) : 80. ScholarBank@NUS Repository. https://doi.org/10.1186/s12981-021-00402-7
dc.identifier.issn1742-6405
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/232699
dc.description.abstractBackground: 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. © 2021, The Author(s).
dc.publisherBioMed Central Ltd
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2021
dc.subjectAbacavir
dc.subjectHIV
dc.subjectMaintenance
dc.subjectRilpivirine
dc.subjectSwitch therapy
dc.subjectVirologically suppressed
dc.typeArticle
dc.contributor.departmentPHARMACY
dc.contributor.departmentMEDICINE
dc.contributor.departmentSAW SWEE HOCK SCHOOL OF PUBLIC HEALTH
dc.description.doi10.1186/s12981-021-00402-7
dc.description.sourcetitleAIDS Research and Therapy
dc.description.volume18
dc.description.issue1
dc.description.page80
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