» Articles » PMID: 34115650

Dolutegravir/lamivudine As a First-line Regimen in a Test-and-treat Setting for Newly Diagnosed People Living with HIV

Abstract

Objectives: Dolutegravir/lamivudine (DTG/3TC) is indicated for treatment-naive and experienced people with HIV; however, questions remain about its utility in a test-and-treat setting because of potential transmitted resistance and baseline hepatitis B virus (HBV) co-infection. We present feasibility and efficacy of DTG/3TC in newly diagnosed individuals in a test-and-treat setting.

Design: The single-arm STAT study evaluated DTG/3TC in a US test-and-treat setting.

Methods: Eligible adults initiated DTG/3TC 14 days or less after HIV-1 diagnosis without availability of baseline laboratory results. If baseline testing indicated DTG or 3TC resistance, HBV co-infection, or creatinine clearance less than 30 ml/min per 1.73 m2, participants remained on study with treatment modification. Efficacy endpoints included proportions of participants with HIV-1 RNA less than 50 copies/ml at Week 24, regardless of antiretroviral regimen, among all participants (intention-to-treat exposed) and those with available HIV-1 RNA data (observed).

Results: Of 131 participants enrolled, 8% were female and 50% were non-white. Through Week 24, treatment was modified in eight participants [five with HBV co-infection, one with baseline M184V, one for adverse event (rash), one participant decision]. At Week 24, 78% (102/131) of all participants and 92% (102/111) of those with available data achieved HIV-1 RNA less than 50 copies/ml. Incidence of drug-related adverse events was low (7%); no drug-related serious adverse events occurred.

Conclusion: These data demonstrate the feasibility, efficacy, and safety of using DTG/3TC as a first-line regimen in a test-and-treat setting, with therapy adjustments for baseline resistance or HBV co-infection occurring safely via routine clinical care as needed [ClinicalTrials.gov, NCT03945981; see Supplemental Digital Content 1, video abstract (Video abstract summarizing the STAT study design and results), http://links.lww.com/QAD/C189].

Citing Articles

24-month outcomes after switching to Dolutegravir/Lamivudine in people living with HIV and HBcAb positivity at the Beijing Ditan Hospital in China.

Fu J, Biao R, Liu Y, Chen J, Zhao H Ann Med. 2025; 57(1):2470957.

PMID: 39992020 PMC: 11852214. DOI: 10.1080/07853890.2025.2470957.


Long-term effectiveness and tolerability of dolutegravir/lamivudine in treatment-naive people with HIV: an analysis of a multicentre cohort at 96 weeks.

Suarez-Garcia I, Alejos B, Moreno C, Martin Torres J, Masia M, Garcia-Fraile L J Antimicrob Chemother. 2024; 80(3):682-691.

PMID: 39710424 PMC: 11879157. DOI: 10.1093/jac/dkae456.


Role of the pharmacist caring for people at risk of or living with HIV in Canada.

Tkachuk S, Ready E, Chan S, Hawkes J, Janzen Cheney T, Kapler J Can Pharm J (Ott). 2024; 157(5):218-239.

PMID: 39310805 PMC: 11412478. DOI: 10.1177/17151635241267350.


Viral load suppression and HIV-1 drug resistance mutations in persons with HIV on TLD/TAFED in Zambia.

Luwaya E, Mwape L, Bwalya K, Siakabanze C, Hamooya B, Masenga S PLoS One. 2024; 19(9):e0308869.

PMID: 39241081 PMC: 11379217. DOI: 10.1371/journal.pone.0308869.


DTG + 3TC dual therapy for the treatment Naïve patients with viral load exceeding 500,000 copies/mL: a retrospective study.

Dou Y, Liao G, Lu R, Su L, Lan K, Meng Z BMC Infect Dis. 2024; 24(1):720.

PMID: 39039487 PMC: 11265357. DOI: 10.1186/s12879-024-09624-2.