Switching to coformulated bictegravir, emtricitabine, and tenofovir alafenamide maintained viral suppression in adults with historical virological failures and K65N/R mutation

Bibliographic Details
Title: Switching to coformulated bictegravir, emtricitabine, and tenofovir alafenamide maintained viral suppression in adults with historical virological failures and K65N/R mutation
Authors: Mao-Song Tsai, Hsin-Yun Sun, Cheng-Pin Chen, Chen-Hsiang Lee, Chun-Yuan Lee, Chun-Eng Liu, Hung-Jen Tang, Tung-Che Hung, Chia-Wen Li, Yuan-Ti Lee, Bo-Huang Liou, Chia-Jui Yang, Chien-Ching Hung
Source: International Journal of Infectious Diseases, Vol 126, Iss , Pp 39-47 (2023)
Publisher Information: Elsevier, 2023.
Publication Year: 2023
Collection: LCC:Infectious and parasitic diseases
Subject Terms: Viral rebound, Low-level viremia, Integrase strand-transfer inhibitor, Nucleoside reverse-transcriptase inhibitor, Resistance-associated mutation, Genetic barrier, Infectious and parasitic diseases, RC109-216
More Details: Objectives: Real-world experience with coformulated bictegravir, emtricitabine, and tenofovir alafenamide (BIC/FTC/TAF) is sparse as a switch regimen among people living with HIV (PLWH) having achieved viral suppression after previous virologic failures with the emergence of K65N/R. Methods: In this retrospective study, PLWH aged ≥20 years who had previous virologic failures with emergent K65N/R were included for switching to BIC/FTC/TAF after having achieved plasma HIV RNA load (PVL) 50 copies/ml) at week 48 using a modified US Food and Drug Administration snapshot algorithm. Results: A total of 72 PLWH with K65N/R who switched to BIC/FTC/TAF were identified. A total of 42 (59.7%) had concurrent M184V/I, and 9 (12.5%) had ≥1 thymidine analog mutations. The median duration of viral suppression was 4.7 years (interquartile range 2.3-5.8), and 97.2% (n = 70) had PVL
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1201-9712
Relation: http://www.sciencedirect.com/science/article/pii/S1201971222005975; https://doaj.org/toc/1201-9712
DOI: 10.1016/j.ijid.2022.11.012
Access URL: https://doaj.org/article/74974abe7a07487f88a22c95815bc8ae
Accession Number: edsdoj.74974abe7a07487f88a22c95815bc8ae
Database: Directory of Open Access Journals
More Details
ISSN:12019712
DOI:10.1016/j.ijid.2022.11.012
Published in:International Journal of Infectious Diseases
Language:English