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https://doi.org/10.1186/s12981-021-00402-7
Title: | Safety and effectiveness of switching to Abacavir/Lamivudine plus rilpivirine for maintenance therapy in virologically suppressed HIV-1 individuals in Singapore (SEALS) | Authors: | 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. |
Keywords: | Abacavir HIV Maintenance Rilpivirine Switch therapy Virologically suppressed |
Issue Date: | 1-Nov-2021 | Publisher: | BioMed Central Ltd | Citation: | 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. (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 | Rights: | Attribution 4.0 International | 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. © 2021, The Author(s). | Source Title: | AIDS Research and Therapy | URI: | https://scholarbank.nus.edu.sg/handle/10635/232699 | ISSN: | 1742-6405 | DOI: | 10.1186/s12981-021-00402-7 | Rights: | Attribution 4.0 International |
Appears in Collections: | Elements Staff Publications |
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