Long-term effectiveness, safety, and tolerability of doravirine in antiretroviral-experienced people with HIV in real life

Real-life data on doravirine (DOR) in different drug combinations are limited. We evaluated the effectiveness of DOR plus two nucleos(t)ide reverse transcriptase inhibitors (NRTI), mainly abacavir/lamivudine, and dual therapies in people with HIV (PWH), mostly virologically suppressed. Ambispective...

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Veröffentlicht in:Microbiology spectrum 2024-08, Vol.12 (8), p.e0065424
Hauptverfasser: Mejías-Trueba, Marta, Gutierrez-Valencia, Alicia, Llaves-Flores, Silvia, Roca-Oporto, Cristina, Herrero, Marta, Sotomayor de la Piedra, César, Lopez-Cortes, Luis F, Espinosa, Nuria
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Sprache:eng
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Zusammenfassung:Real-life data on doravirine (DOR) in different drug combinations are limited. We evaluated the effectiveness of DOR plus two nucleos(t)ide reverse transcriptase inhibitors (NRTI), mainly abacavir/lamivudine, and dual therapies in people with HIV (PWH), mostly virologically suppressed. Ambispective observational study that enrolled adults PWH who initiated a DOR-based regimen from September 2020 to February 2022 at a referral center in Spain. Participants were grouped as follows: A, received DOR plus two NRTI; B, dual therapy (DT) with DOR plus dolutegravir (DTG) or darunavir/cobicistat (DRVc); C, DOR plus ≥two antiretroviral drugs. The primary endpoints were treatment effectiveness at week 48 by intention-to-treat (ITT) and per-protocol analysis (OT). A cohort of 187 participants, 91% virologically suppressed, were analyzed after a median follow-up of 112 weeks (80-136). Group A received DOR plus abacavir/lamivudine (ABV/3TC) ( = 109) or tenofovir/emtricitabine (TFV/3TC) ( = 45). At week 48, the effectiveness of DOR plus ABV/3TC by ITT was 90.8% (CI , 88.0-93.6), better than with TFV/FTC [73.3% (66.7-79.9); = 0.003]. Only one virologic failure was observed. Mild adverse effects were the cause of treatment discontinuation in 7.8%, followed by switching to a single-tablet regimen. In group B, the effectiveness by ITT was 92.9% (CI , 88.0-97.8) at week 48. No adverse effects or virologic failure were registered in this group. DOR plus two NRTI or DT have long-term effectiveness and safety as a switching option for PWH, mostly virologically suppressed. The DOR plus ABV/3TC combination has shown even better effectiveness than TFV/FTC.IMPORTANCEDOR-based regimens have shown long-term effectiveness and safety in PWH, mostly virologically suppressed. The combination of DOR plus ABV/3TC has shown even better safety and effectiveness than TFV/FTC. DOR plus two NRTI offers cost benefits compared to other regimens.
ISSN:2165-0497
2165-0497
DOI:10.1128/spectrum.00654-24