DAA-based treatment for HIV-HCV-coinfected patients: analysis of factors of sustained virological response in a real-life study.


Journal

Antiviral therapy
ISSN: 2040-2058
Titre abrégé: Antivir Ther
Pays: England
ID NLM: 9815705

Informations de publication

Date de publication:
2020
Historique:
accepted: 05 02 2020
pubmed: 22 4 2020
medline: 26 10 2021
entrez: 22 4 2020
Statut: ppublish

Résumé

The aim of the present study was to evaluate in HIV-infected patients treated with a direct-acting antiviral agent (DAA)-based regimen the variables associated with sustained virological response (SVR) and the trend in biochemical parameters and clinical events during and after DAA regimen. We performed a multicentre retrospective cohort study, enrolling all 243 HIV-HCV-coinfected adult patients treated with DAAs between January 2015 and December 2018 in one of the nine participating Infectious Disease Centers in southern Italy, eight in Campania and one in Apulia. Of the 243 patients enrolled, 233 (95.9%) obtained an SVR at 12 weeks (SVR12). Of the 10 patients with non-SVR, 7 were tested for NS3, NS5A and NS5B resistance-associated substitutions (RASs) by sequencing analysis and 6 showed at least 1 major RAS in 1 HCV region (all in NS5A, 2 in NS5B and 1 in NS3). Comparing the 233 patients achieving SVR and the 10 non-achievers, no variable was independently associated with non-SVR. During and after DAA regimen, no modification in the biochemical parameters and clinical events was observed; however, the serum cholesterol and low-density lipoprotein (LDL) levels showed an increase (from 159 ±41.3 mg/dl at baseline to 174 ±44.5 mg/dl at week 12 after stopping treatment, P<0.001, and from 92 ±34.6 mg/dl to 109.4 ±73.7 mg/dl, P=0.002, respectively). The treatment with DAAs led to a high SVR12 rate in HIV-HCV-coinfected subjects, irrespective of epidemiological, clinical or virological characteristics. However, the DAA regimen was associated with an increase in total- and LDL-cholesterol, to be taken into account in the management of HIV infection.

Sections du résumé

BACKGROUND
The aim of the present study was to evaluate in HIV-infected patients treated with a direct-acting antiviral agent (DAA)-based regimen the variables associated with sustained virological response (SVR) and the trend in biochemical parameters and clinical events during and after DAA regimen.
METHODS
We performed a multicentre retrospective cohort study, enrolling all 243 HIV-HCV-coinfected adult patients treated with DAAs between January 2015 and December 2018 in one of the nine participating Infectious Disease Centers in southern Italy, eight in Campania and one in Apulia.
RESULTS
Of the 243 patients enrolled, 233 (95.9%) obtained an SVR at 12 weeks (SVR12). Of the 10 patients with non-SVR, 7 were tested for NS3, NS5A and NS5B resistance-associated substitutions (RASs) by sequencing analysis and 6 showed at least 1 major RAS in 1 HCV region (all in NS5A, 2 in NS5B and 1 in NS3). Comparing the 233 patients achieving SVR and the 10 non-achievers, no variable was independently associated with non-SVR. During and after DAA regimen, no modification in the biochemical parameters and clinical events was observed; however, the serum cholesterol and low-density lipoprotein (LDL) levels showed an increase (from 159 ±41.3 mg/dl at baseline to 174 ±44.5 mg/dl at week 12 after stopping treatment, P<0.001, and from 92 ±34.6 mg/dl to 109.4 ±73.7 mg/dl, P=0.002, respectively).
CONCLUSIONS
The treatment with DAAs led to a high SVR12 rate in HIV-HCV-coinfected subjects, irrespective of epidemiological, clinical or virological characteristics. However, the DAA regimen was associated with an increase in total- and LDL-cholesterol, to be taken into account in the management of HIV infection.

Identifiants

pubmed: 32314978
doi: 10.3851/IMP3353
doi:

Substances chimiques

Antiviral Agents 0
Viral Nonstructural Proteins 0

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

193-201

Auteurs

Loredana Alessio (L)

Infectious Diseases Unit, AORN Sant'Anna e San Sebastiano, Caserta, Italy.

Lorenzo Onorato (L)

Infectious Diseases Unit, AORN Sant'Anna e San Sebastiano, Caserta, Italy.
Department of Mental Health and Preventive Medicine, Section of Infectious Diseases, University of Campania "L. Vanvitelli", Naples, Italy.

Vincenzo Sangiovanni (V)

Third Infectious Diseases Unit, AORN dei Colli, P.O. Cotugno, Naples, Italy.

Francesco Borrelli (F)

Infectious Diseases Unit, University Federico II, Naples, Italy.

Elio Manzillo (E)

VIII Infectious Diseases Unit, AORN dei Colli, P.O. Cotugno, Naples, Italy.

Vincenzo Esposito (V)

Immunodeficiency and Gender Related Infectious Diseases Unit, Department of Infectious Disease and Infectious Emergencies, AORN dei Colli, P.O. Cotugno, Naples, Italy.

Filomena Simeone (F)

Infectious Diseases Unit, AORN Sant'Anna e San Sebastiano, Caserta, Italy.

Salvatore Martini (S)

Department of Mental Health and Preventive Medicine, Section of Infectious Diseases, University of Campania "L. Vanvitelli", Naples, Italy.

Nicolina Capoluongo (N)

Department of Mental Health and Preventive Medicine, Section of Infectious Diseases, University of Campania "L. Vanvitelli", Naples, Italy.

Sebastiano Leone (S)

Infectious Diseases Unit, A.O. S.G. Moscati, Avellino, Italy.

Giovanni Di Filippo (G)

Infectious Diseases Unit, University Federico II, Naples, Italy.

Maurizio D'Abbraccio (M)

Immunodeficiency and Gender Related Infectious Diseases Unit, Department of Infectious Disease and Infectious Emergencies, AORN dei Colli, P.O. Cotugno, Naples, Italy.

Lucia Aprea (L)

VIII Infectious Diseases Unit, AORN dei Colli, P.O. Cotugno, Naples, Italy.

Angelo Salomone Megna (AS)

Infectious Diseases Unit, A.O. G. Rummo, Benevento, Italy.

Eugenio Milano (E)

Department of Biomedical Sciences and Human Oncology, Clinic of Infectious Diseases, University of Bari, Bari, Italy.

Viviana Rizzo (V)

Immunodeficiency and Gender Related Infectious Diseases Unit, Department of Infectious Disease and Infectious Emergencies, AORN dei Colli, P.O. Cotugno, Naples, Italy.

Annalisa Saracino (A)

Department of Biomedical Sciences and Human Oncology, Clinic of Infectious Diseases, University of Bari, Bari, Italy.

Nicola Coppola (N)

Infectious Diseases Unit, AORN Sant'Anna e San Sebastiano, Caserta, Italy.
Department of Mental Health and Preventive Medicine, Section of Infectious Diseases, University of Campania "L. Vanvitelli", Naples, Italy.

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