Durability of doravirine with dolutegravir dual regimen compared with other dolutegravir‐based dual combinations

Author:

Rossotti Roberto1ORCID,D'Amico Federico1,Bana Nicholas Brian12,Nava Alice3,Rezzonico Leonardo Francesco14,Raimondi Alessandro1,Fanti Diana3,Chianura Leonardo Gerolamo1,Moioli Maria Cristina1,Vismara Chiara3,Puoti Massimo12

Affiliation:

1. Department of Infectious Diseases ASST Grande Ospedale Metropolitano Niguarda Milan Italy

2. School of Medicine University of Milan‐Bicocca Milan Italy

3. Clinical Microbiology ASST Grande Ospedale Metropolitano Niguarda Milan Italy

4. School of Medicine University of Pavia Pavia Italy

Abstract

AbstractObjectivesThe availability of doravirine (DOR) allowed clinicians to prescribe a dolutegravir (DTG)‐based two‐drug regimen (2DR) in individuals not eligible to receive lamivudine (3TC) or rilpivirine (RPV). The aims of this study were to describe the durability of DTG + DOR compared with DTG/3TC and DTG/RPV and the rate of virological failure and target not‐detected maintenance over time.MethodsThis retrospective, monocentric analysis included all subjects who started a DTG‐based 2DR from 2018 to 2022 as a simplification. Descriptive statistics and non‐parametric tests to describe and compare the groups were applied. Kaplan–Meier probability curves and Cox regression models for regimens durability were used.ResultsThe study enrolled 710 individuals: 499 treated with DTG/3TC, 140 with DTG/RPV, and 71 with DTG + DOR. A 2DR with DOR was prescribed to older subjects who had a longer infection, greater exposure to different antiretroviral regimens, a higher proportion of resistance‐associated mutations, and a worse immune‐virologic status. Over a cumulative follow‐up of 68 152 weeks, 42 discontinuations were registered (5.9%). DTG + DOR had a risk of treatment interruption of 7.8% at 48 weeks and 9.8% at 96 weeks, significantly higher than the other 2DRs. In the multivariate Cox model, DTG + DOR and DTG/RPV were significantly associated with discontinuation. The maintenance of target not detected during follow‐up was similar among groups. The rate of virological failure was higher for DTG + DOR through different event definitions.ConclusionsDTG + DOR durability was high over a long follow‐up albeit lower than for other 2DRs. This combination might be an effective option in people with HIV that has proven difficult to treat.

Publisher

Wiley

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