Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/56516
Title: Decline in CD4 T lymphocytes with monotherapy bridging strategy for non-adherent adolescents living with HIV infection: Results of the IMPAACT P1094 randomized trial
Authors: Allison L. Agwu
Meredith G. Warshaw
Elizabeth J. McFarland
George K. Siberry
Ann J. Melvin
Andrew A. Wiznia
Lee Fairlie
Sandra Boyd
Paul Harding
Hans M.L. Spiegel
Elaine J. Abrams
Vincent J. Carey
Murli Purswani
Linda Aurpibul
Virat Sirisanthana
Chintana Khamrong
Joan Wilson
Margaret Donnelly
John Swetnam
Erica Stankievich
Silvina A. Ivalo
Irene Foradori
Ivete Martins Gomes
Jose Henrique Pilotto
Cintia Lopes Da Silva
Marinella Della Negra
Yu Ching Lian
Denise Peluso Pacola
Thuy C. Anderson
Todd C. Noletto
Keywords: Agricultural and Biological Sciences
Biochemistry, Genetics and Molecular Biology
Issue Date: 1-Jun-2017
Abstract: Introduction: Management of persistently non-adherent youth living with HIV (YLHIV) with virologic failure (VF) on combination antiretroviral therapy (cART) remains challenging. One strategy has been using 3TC/FTC monotherapy (3TC/FTC), which in the presence of the M184V resistance mutation, does not suppress viral replication nor select for additional drug resistance mutations, and reduces viral fitness with limited side effects. P1094 compared the immunologic outcome of continuing failing cART vs. switching to 3TC/FTC as a "bridging strategy" to subsequent suppressive cART for non-adherent YLHIV with pre-existing M184V resistance. Materials & methods: Participants with documented nonadherence, M184V mutation, CD4+T cell count ≥100 cells/mm3and VF (HIV-1 plasma RNA ≥400 copies/mL (2.6 log10HIV-1 RNA) were enrolled and randomized to continue failing cART vs. switch to 3TC/FTC. The primary endpoint (time to ≥30% CD4+T cell decline or development of CDC class C events) at 28-weeks were assessed by Kaplan-Meier (K-M) curves in an intent-to-treat analysis. Results: Thirty-three perinatally acquired YLHIV participants (16 continuing cART and 17 3TC/FTC) enrolled in the study. The median age, entry CD4+T cell count, and viral load were 15 years (Inter-quartile range (IQR) 14-20), 472 cells/mm3(IQR 384-651), and 4.0 log10HIV-1 RNA copies/ml (IQR 3.2-4.5), respectively. Five participants, all in the 3TC/FTC arm, reached the primary endpoint for absolute CD4+T cell decline (p = 0.02, exact log-rank test comparing monotherapy to cART). The Kaplan-Meier estimate of probability of primary endpoint on 3TC/FTC at 28 weeks was 0.41 (standard error 0.14). There were no CDC class C events or deaths and no statistically significant difference in frequencies of adverse events between the arms. Conclusions: Non-adherent participants randomized to 3TC/FTC were more likely than those maintained on failing cART to experience a confirmed decline in CD4+count of ≥30%. Although this study suffers from limitations of small sample size and premature discontinuation, the randomized comparison to continuing failing cART indicates that 3TC/FTC provides inferior protection from immunologic deterioration for non-adherent youth with M184V resistance. Better alternatives to 3TC/FTC such as ART with higher barriers to resistance and novel adherence and treatment strategies for nonadherent youth are urgently needed. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85020697190&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/56516
ISSN: 19326203
Appears in Collections:CMUL: Journal Articles

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