Abstract
In the ASPIRE trial, antiretroviral therapy (ART) switch to dolutegravir plus lamivudine (DTG+3TC) was comparable to 3-drug ART in maintaining viral suppression by standard viral load assays. We used an ultrasensitive assay to assess whether this switch led to increased residual viremia. At entry, levels of residual viremia did not differ significantly between arms (DTG+3TC vs 3-drug ART: mean, 5.0 vs 4.2 HIV-1 RNA copies/mL; P = .64). After randomization, no significant between-group differences were found at either week 24 or 48. These results show no evidence for increased viral replication on DTG+3TC and support its further investigation as a dual ART strategy.
Original language | English (US) |
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Article number | 56 |
Journal | Open Forum Infectious Diseases |
Volume | 6 |
Issue number | 3 |
DOIs | |
State | Published - Mar 2019 |
Funding
This work was supported by an investigator-sponsored study grant from ViiV HealthCare to Northwestern University (NU). V.C.M., C.J.F., C.A.B., T.W., S.L.K., J.C., J.Z.L., and P.E.S. have received grant funding for this study to their institutions through NU from ViiV/GSK. V.C.M. has received funding from the Emory CFAR (P30AI050409).
Keywords
- ART simplification
- ART switch
- Dolutegravir
- Lamivudine
- Residual viremia
ASJC Scopus subject areas
- Infectious Diseases
- Oncology