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  4. Three-year durable efficacy of dolutegravir plus lamivudine in antiretroviral therapy - naive adults with hiv-1 infection
 
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Three-year durable efficacy of dolutegravir plus lamivudine in antiretroviral therapy - naive adults with hiv-1 infection

Journal
AIDS
Journal Volume
36
Journal Issue
1
Pages
39-48
Date Issued
2022
Author(s)
Cahn P.
Sierra Madero J.
Arribas J.R.
Antinori A.
Ortiz R.
Clarke A.E.
CHIEN-CHING HUNG  
Rockstroh J.K.
Girard P.-M.
Sievers J.
Man C.Y.
Urbaityte R.
Brandon D.J.
Underwood M.
Pappa K.A.
Curtis L.
Smith K.Y.
Gartland M.
Aboud M.
Van Wyk J.
Wynne B.
DOI
10.1097/QAD.0000000000003070
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85120899525&doi=10.1097%2fQAD.0000000000003070&partnerID=40&md5=d4ac9bb9fc792d70a401991c599198ec
https://scholars.lib.ntu.edu.tw/handle/123456789/620516
Abstract
OBJECTIVE: To assess efficacy and safety of dolutegravir (DTG) + lamivudine (3TC) vs. DTG + tenofovir disoproxil fumarate/emtricitabine (TDF/FTC) in treatment-naive adults with HIV-1 in the prespecified 144-week secondary analyses of GEMINI-1 and GEMINI-2. DESIGN: Identical, multicenter, phase III, randomized, non-inferiority studies (double-blind through 96 weeks). METHODS: Participants with HIV-1 RNA ≤500 000 copies/ml and no major viral resistance mutations to nucleoside reverse transcriptase inhibitors, nonnucleoside reverse transcriptase inhibitors, or protease inhibitors were randomized 1:1 to once-daily DTG + 3TC or DTG + TDF/FTC. RESULTS: At week 144, DTG + 3TC (N = 716) was noninferior to DTG + TDF/FTC (N = 717) in proportion of participants achieving HIV-1 RNA <50 copies/ml (Snapshot algorithm) in the pooled analysis (82% vs. 84%, respectively; adjusted treatment difference [95% confidence interval (CI)], -1.8% [-5.8, 2.1]), GEMINI-1 (-3.6% [-9.4, 2.1]), and GEMINI-2 (0.0% [-5.3, 5.3]). Twelve DTG + 3TC participants and nine DTG + TDF/FTC participants met protocol-defined confirmed virologic withdrawal (CVW) criteria; none developed treatment-emergent resistance. One DTG + 3TC participant who did not meet CVW criteria developed M184V at week 132 and R263R/K at week 144, conferring a 1.8-fold change in susceptibility to DTG; non-adherence to therapy was reported. Significantly fewer drug-related adverse events occurred with DTG + 3TC vs. DTG + TDF/FTC (20% vs. 27%; relative risk [95% CI], 0.76 [0.63-0.92]). Renal and bone biomarker changes favored DTG + 3TC. CONCLUSIONS: Three-year durable efficacy, long-term tolerability, and high barrier to resistance support first-line use of DTG + 3TC for HIV-1 treatment (see Supplemental Digital Content 1, http://links.lww.com/QAD/C297; video abstract).
SDGs

[SDGs]SDG3

Publisher
Lippincott Williams and Wilkins
Type
journal article

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