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Durable Efficacy of Switching From a 3- or 4-Drug Tenofovir Alafenamide-Based Regimen to the 2-Drug Regimen Dolutegravir/Lamivudine in the TANGO Study Through Week 196.
De Wit, Stéphane; Bonnet, Fabrice; Osiyemi, Olayemi; Bisshop, Fiona; Olalla, Julian; Routy, Jean-Pierre; Wyen, Christoph; Moodley, Riya; Pappa, Keith; Wang, Ruolan; Oyee, James; Saggu, Parminder; Letang, Emilio; Wynne, Brian; Jones, Bryn; Smith, Kimberly Y; Ait-Khaled, Mounir.
Affiliation
  • De Wit S; CHU Saint-Pierre, Université Libre de Bruxelles, Brussels, Belgium.
  • Bonnet F; CHU de Bordeaux, Service de Médecine Interne et Maladies Infectieuses, and Bordeaux University, INSERM U1219, Bordeaux Population Health, Bordeaux, France.
  • Osiyemi O; Triple O Research Institute PA, West Palm Beach, FL, USA.
  • Bisshop F; Holdsworth House Medical Brisbane, Queensland, Australia.
  • Olalla J; Unidad de Medicina Interna, Hospital Costa del Sol, Marbella, Spain.
  • Routy JP; McGill University Health Centre, Montréal, QC, Canada.
  • Wyen C; Praxis am Ebertplatz, Cologne, Germany.
  • Moodley R; ViiV Healthcare, Brentford, UK.
  • Pappa K; ViiV Healthcare, Durham, NC, USA.
  • Wang R; ViiV Healthcare, Durham, NC, USA.
  • Oyee J; GSK, Brentford, UK.
  • Saggu P; GSK, Brentford, UK.
  • Letang E; ViiV Healthcare, Madrid, Spain.
  • Wynne B; ViiV Healthcare, Durham, NC, USA.
  • Jones B; ViiV Healthcare, Brentford, UK.
  • Smith KY; ViiV Healthcare, Durham, NC, USA.
  • Ait-Khaled M; ViiV Healthcare, Brentford, UK.
Article in En | MEDLINE | ID: mdl-38346427
ABSTRACT

BACKGROUND:

Switching to the 2-drug regimen dolutegravir/lamivudine demonstrated durable non-inferior efficacy vs continuing 3- or 4-drug tenofovir alafenamide-based regimens for maintaining virologic suppression in people with HIV-1 through Week 144 in TANGO.

SETTING:

134 centers, 10 countries.

METHODS:

Adults with HIV-1 RNA <50 copies/mL for >6 months and no history of virologic failure were randomized to switch from stable tenofovir alafenamide-based regimens to dolutegravir/lamivudine on Day 1 (early-switch group) for 196 weeks. Those randomized to continue tenofovir alafenamide-based regimens on Day 1 who maintained virologic suppression at Week 144 switched to dolutegravir/lamivudine at Week 148 (late-switch group). Efficacy, safety, and tolerability (including weight and biomarker changes) of dolutegravir/lamivudine in early-switch and late-switch groups were assessed through Week 196.

RESULTS:

Overall, 369 participants switched to dolutegravir/lamivudine on Day 1 (early-switch) and 298 switched at Week 148 (late-switch). In the early-switch group, 83% (306/369) maintained virologic suppression through Year 4, and 3% (11/369) reported new adverse events between Weeks 144 and 196. The late-switch group at Week 196 and early-switch group at Week 48 had comparable proportions with virologic suppression (93% each) and similar safety profiles. No late-switch participants and 1 early-switch participant met confirmed virologic withdrawal criteria through Week 196, with no resistance-associated mutations observed. Treatment continued to be well tolerated long-term.

CONCLUSION:

Switching from tenofovir alafenamide-based regimens to dolutegravir/lamivudine showed durable efficacy, high barrier to resistance, and good tolerability through 4 years. These results support dolutegravir/lamivudine as a robust treatment for maintaining virologic suppression.

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials Language: En Journal: J Acquir Immune Defic Syndr Journal subject: SINDROME DA IMUNODEFICIENCIA ADQUIRIDA (AIDS) Year: 2024 Type: Article Affiliation country: Belgium

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials Language: En Journal: J Acquir Immune Defic Syndr Journal subject: SINDROME DA IMUNODEFICIENCIA ADQUIRIDA (AIDS) Year: 2024 Type: Article Affiliation country: Belgium