Effect of mono/dual antiretroviral therapy on suppression of HCV and HIV during treatment of HCV infection in HIV/HCV-coinfected patients.


Journal

Enfermedades infecciosas y microbiologia clinica (English ed.)
ISSN: 2529-993X
Titre abrégé: Enferm Infecc Microbiol Clin (Engl Ed)
Pays: Spain
ID NLM: 101777541

Informations de publication

Date de publication:
Historique:
received: 12 06 2018
revised: 23 09 2018
accepted: 27 09 2018
pubmed: 28 11 2018
medline: 31 7 2020
entrez: 28 11 2018
Statut: ppublish

Résumé

Data of hepatitis C treatment with direct-acting antivirals (DAAs) in HIV infected patients are limited to a few number of antiretroviral therapies (ART). The aim of this study was to assess the effectiveness and safety of non-conventional ART as monotherapy or dual therapy (MDT) when combined with DAA. Retrospective review of HIV/HCV-coinfected patients treated with DAAs during one year in 3 centers. Sustained virologic response 12 weeks after therapy (SVR) and maintenance of HIV viral suppression were compared between patients receiving triple ART (TT) or MDT. Overall 485 patients were included (359 receiving TT and 126 MDT). HCV SVR was 93.4% (95%CI, 90.8% to 95.3%) in the intention-to-treat analysis without differences between groups: 92.8% on TT vs 95.2% on MDT (p=0.3). HCV virological failure was associated with lower CD4+cell count at baseline (for every 100-cell/μl increment: OR, 0.8; 95%CI, 0.7-0.9; p=0.01) and with liver stiffness (for every 10-unit increment: OR, 1.5; 95%CI 1.2-1.8; p<0.01). HIV-RNA during HCV treatment or 12 weeks after was detectable in 23 patients on TT (6.6%) and 9 (7.2%) patients on MDT (p=0.8). The median (IQR) change in CD4+cell count was not significantly different between the groups: 15 (-55 to 115) in TT vs -12 (-68 to 133) cells/μl in MDT (p=0.8). DAAs obtain high rates of SVR among HIV/HCV-coinfected patients independently of whether TT or non-conventional ART is used. Suppression of HIV was maintained in both groups.

Identifiants

pubmed: 30477904
pii: S0213-005X(18)30277-5
doi: 10.1016/j.eimc.2018.09.013
pii:
doi:

Substances chimiques

Antiviral Agents 0
Drug Combinations 0

Types de publication

Journal Article Multicenter Study

Langues

eng spa

Sous-ensembles de citation

IM

Pagination

367-372

Informations de copyright

Copyright © 2018 Elsevier España, S.L.U. and Sociedad Española de Enfermedades Infecciosas y Microbiología Clínica. All rights reserved.

Auteurs

Luz Martín-Carbonero (L)

Unidad de VIH, Servicio Medicina Interna, Hospital Universitario La Paz, Madrid, IdiPaz. Electronic address: lmcarbonero@gmail.com.

Lourdes Domínguez-Domínguez (L)

Unidad de VIH, Servicio Medicina Interna, Hospital Universitario Doce de Octubre, Madrid, IMAS12.

Lucía Bailón (L)

Unidad de VIH, Servicio Medicina Interna, Hospital Universitario La Paz, Madrid, IdiPaz.

Rafael Torres (R)

Unidad de VIH, Servicio Medicina Interna, Hospital Universitario Severo Ochoa, Leganés.

Rafael Rubio (R)

Unidad de VIH, Servicio Medicina Interna, Hospital Universitario Doce de Octubre, Madrid, IMAS12.

Raquel Ron (R)

Unidad de VIH, Servicio Medicina Interna, Hospital Universitario La Paz, Madrid, IdiPaz.

Francisco Moreno (F)

Servicio de Farmacia, Hospital Universitario La Paz, Madrid, IdiPaz.

Mikel Rico (M)

Unidad de VIH, Servicio Medicina Interna, Hospital Universitario La Paz, Madrid, IdiPaz.

Inmaculada Jimenez-Nacher (I)

Servicio de Farmacia, Hospital Universitario La Paz, Madrid, IdiPaz.

Juan González-García (J)

Unidad de VIH, Servicio Medicina Interna, Hospital Universitario La Paz, Madrid, IdiPaz.

Federico Pulido (F)

Unidad de VIH, Servicio Medicina Interna, Hospital Universitario Doce de Octubre, Madrid, IMAS12.

María Luisa Montes (ML)

Unidad de VIH, Servicio Medicina Interna, Hospital Universitario La Paz, Madrid, IdiPaz.

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Classifications MeSH