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

Author:

Mejías-Trueba Marta1ORCID,Gutierrez-Valencia Alicia23,Llaves-Flores Silvia2,Roca-Oporto Cristina2,Herrero Marta2,Sotomayor de la Piedra César2,Lopez-Cortes Luis F.2ORCID,Espinosa Nuria2

Affiliation:

1. Department of Pharmacy, University Hospital Virgen del Rocío, Seville, Spain

2. Infectious Diseases and Microbiology Clinical Unit. Instituto de Biomedicina de Sevilla/University Hospital Virgen del Rocío/CSIC/Universidad de Sevilla, Sevilla, Spain

3. Primary Care Pharmacist Service, Sevilla Primary Care District, Sevilla, Spain

Abstract

ABSTRACT 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) ( n = 109) or tenofovir/emtricitabine (TFV/3TC) ( n = 45). At week 48, the effectiveness of DOR plus ABV/3TC by ITT was 90.8% (CI 95 , 88.0–93.6), better than with TFV/FTC [73.3% (66.7–79.9); P = 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 95 , 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. IMPORTANCE DOR-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.

Funder

MEC | Instituto de Salud Carlos III

Publisher

American Society for Microbiology

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