Effectiveness and Tolerability of DOR/3TC/TDF in Experienced People with HIV Switching from RPV/FTC/TDF: A Retrospective, Single Center Cohort Study
2024

Effectiveness of Switching HIV Treatment to DOR/3TC/TDF

Sample size: 426 publication 10 minutes Evidence: moderate

Author Information

Author(s): Cicalini Stefania, Lanini Simone, Gagliardini Roberta, Bellagamba Rita, Vergori Alessandra, Mastrorosa Ilaria, Mazzotta Valentina, Esvan Rozenn, Plazzi Maria Maddalena, Ottou Sandrine, Grilli Elisabetta, De Zottis Federico, Fusto Marisa, Paulicelli Jessica, Antinori Andrea, Berzal-Herranz Alfredo, Resino Salvador, Sepúlveda-Crespo Daniel

Primary Institution: National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS

Hypothesis

Is switching to a regimen of doravirine (DOR), tenofovir disoproxil fumarate (TDF), and lamivudine (3TC) effective for people living with HIV who are experienced with other treatments?

Conclusion

Switching to DOR/3TC/TDF from RPV/TDF/FTC is effective and well-tolerated for people living with HIV.

Supporting Evidence

  • The treatment failure rate was only 2.34%.
  • CD4 counts improved significantly by about 50 cells/µL.
  • The regimen did not cause adverse metabolic effects.
  • Most participants maintained viral suppression.
  • Switching to DOR/3TC/TDF was well-tolerated.
  • Participants had been virologically suppressed for a median of 6 years.
  • Significant improvements were observed in immunological parameters.
  • The study supports ongoing research for ART regimens.

Takeaway

This study shows that changing HIV treatment to a new combination of drugs can help people stay healthy without causing bad side effects.

Methodology

This was a retrospective cohort study analyzing 426 people living with HIV who switched from RPV/FTC/TDF to DOR/3TC/TDF.

Potential Biases

Potential biases associated with retrospective data collection and lack of a control group.

Limitations

The study's retrospective design and single-center setting may limit the generalizability of the findings.

Participant Demographics

Median age was 47 years, with 69.48% males and 14.79% non-Caucasian individuals.

Statistical Information

P-Value

p < 0.001

Confidence Interval

95% CI, 1.28–4.50%

Statistical Significance

p < 0.001

Digital Object Identifier (DOI)

10.3390/ph17121706

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