No Significant Changes to Residual Viremia After Switch to Dolutegravir and Lamivudine in a Randomized Trial

Author:

Li Jonathan Z1ORCID,Sax Paul E1,Marconi Vincent C2,Fajnzylber Jesse1,Berzins Baiba3,Nyaku Amesika N4ORCID,Fichtenbaum Carl J5,Wilkin Timothy6,Benson Constance A7,Koletar Susan L8,Lorenzo-Redondo Ramon3,Taiwo Babafemi O3

Affiliation:

1. Division of Infectious Diseases, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachussetts

2. Division of Infectious Diseases, Emory University School of Medicine and Rollins School of Public Health, Atlanta, Georgia

3. Division of Infectious Diseases, Northwestern University, Chicago, Illinois

4. Division of Infectious Diseases, Rutgers University, Newark, New Jersey

5. Division of Infectious Diseases, University of Cincinnati, Cincinnati, Ohio

6. Division of Infectious Diseases, Weill Cornell Medicine, New York, New York

7. Division of Infectious Diseases, University of California, San Diego, California

8. Division of Infectious Diseases, Ohio State University, Columbus, Ohio

Abstract

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.

Funder

Emory CFAR

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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