Very high pre-therapy viral load is a predictor of virological rebound in HIV-1-infected patients starting a modern first-line regimen.


Journal

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

Informations de publication

Date de publication:
2019
Historique:
accepted: 27 02 2019
pubmed: 13 4 2019
medline: 7 7 2020
entrez: 13 4 2019
Statut: ppublish

Résumé

Pre-cART (combined antiretroviral therapy) plasma viral load >500,000 copies/ml has been associated with a lower probability of achieving virological suppression, while few data about its role on maintenance of virological suppression are available. In this study we aimed to clarify whether high levels of pre-cART viraemia are associated with virological rebound (VR) after virological suppression. HIV-infected individuals who achieved virological suppression after first-line cART were included. VR was defined as the first of two consecutive viraemia >50 copies/ml (VR50) or, in an alternative analysis, >200 copies/ml (VR200). The impact of pre-cART viraemia on the risk of VR was evaluated by survival analyses. Among 5,766 patients included, 59.2%, 31.4%, 5.2% and 4.2% had pre-cART viraemia ≤100,000, 100,001-500,000, 500,001-1,000,000 and >1,000,000 copies/ml, respectively. Patients with pre-cART viraemia levels >1,000,000 copies/ml had the highest probability of VR (>1,000,000; 500,000-1,000,000; 100,000-500,000; <100,000 copies/ml; VR50: 28.4%; 24.3%; 17.6%; 13.8%, P<0.0001; VR200: 14.4%; 11.1%; 7.2%; 7.6%; P=0.009). By Cox multivariable analyses, patients with pre-cART viraemia >500,000 and >1,000,000 copies/ml showed a significantly higher risk of VR regardless of the VR end point used. No difference in the risk of VR was found between patients with pre-cART viraemia ranging 500,000-1,000,000 copies/ml and those with pre-cART viraemia >1,000,000 copies/ml, regardless of the VR end point used. Pre-cART plasma viral load levels >500,000 copies/ml can identify fragile patients with poorer chance of maintaining virological control after an initial response. An effort in defining effective treatment strategies is mandatory for these patients that remain difficult to treat.

Sections du résumé

BACKGROUND
Pre-cART (combined antiretroviral therapy) plasma viral load >500,000 copies/ml has been associated with a lower probability of achieving virological suppression, while few data about its role on maintenance of virological suppression are available. In this study we aimed to clarify whether high levels of pre-cART viraemia are associated with virological rebound (VR) after virological suppression.
METHODS
HIV-infected individuals who achieved virological suppression after first-line cART were included. VR was defined as the first of two consecutive viraemia >50 copies/ml (VR50) or, in an alternative analysis, >200 copies/ml (VR200). The impact of pre-cART viraemia on the risk of VR was evaluated by survival analyses.
RESULTS
Among 5,766 patients included, 59.2%, 31.4%, 5.2% and 4.2% had pre-cART viraemia ≤100,000, 100,001-500,000, 500,001-1,000,000 and >1,000,000 copies/ml, respectively. Patients with pre-cART viraemia levels >1,000,000 copies/ml had the highest probability of VR (>1,000,000; 500,000-1,000,000; 100,000-500,000; <100,000 copies/ml; VR50: 28.4%; 24.3%; 17.6%; 13.8%, P<0.0001; VR200: 14.4%; 11.1%; 7.2%; 7.6%; P=0.009). By Cox multivariable analyses, patients with pre-cART viraemia >500,000 and >1,000,000 copies/ml showed a significantly higher risk of VR regardless of the VR end point used. No difference in the risk of VR was found between patients with pre-cART viraemia ranging 500,000-1,000,000 copies/ml and those with pre-cART viraemia >1,000,000 copies/ml, regardless of the VR end point used.
CONCLUSIONS
Pre-cART plasma viral load levels >500,000 copies/ml can identify fragile patients with poorer chance of maintaining virological control after an initial response. An effort in defining effective treatment strategies is mandatory for these patients that remain difficult to treat.

Identifiants

pubmed: 30977466
doi: 10.3851/IMP3309
doi:

Substances chimiques

Anti-HIV Agents 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

321-331

Auteurs

Daniele Armenia (D)

Department of Experimental Medicine, University of Rome 'Tor Vergata', Rome, Italy.
Saint Camillus International University of Health Sciences, Rome, Italy.

Domenico Di Carlo (D)

Pediatric Clinical Research Center 'Romeo and Erica Invernizzi', University of Milan, Milan, Italy.

Alessandro Cozzi-Lepri (A)

Institute for Global Health London, University College London, London, UK.

Andrea Calcagno (A)

Unit of Infectious Diseases, Department of Medical Sciences, University of Turin, Turin, Italy.

Vanni Borghi (V)

Clinic of Infectious Diseases, University Hospital, University of Modena and Reggio Emilia, Modena, Italy.

Caterina Gori (C)

Virology Unit, National Institute for Infectious Diseases L. Spallanzani, IRCCS, Rome, Italy.

Ada Bertoli (A)

Department of Experimental Medicine, University of Rome 'Tor Vergata', Rome, Italy.

William Gennari (W)

Microbiology and Virology Unit, University Hospital Polyclinic, Modena, Italy.

Rita Bellagamba (R)

Clinical Division of HIV/AIDS, National Institute for Infectious Diseases L. Spallanzani, IRCCS, Rome, Italy.

Antonella Castagna (A)

Infectious Diseases Department, IRCCS San Raffaele Scientific Institute & Vita-Salute University, Milan, Italy.

Alessandra Latini (A)

Unit of Dermatology and Sexually Transmitted Diseases, San Gallicano Dermatological Institute IRCCS, Rome, Italy.

Carmela Pinnetti (C)

Clinical Division of HIV/AIDS, National Institute for Infectious Diseases L. Spallanzani, IRCCS, Rome, Italy.

Stefania Cicalini (S)

Clinical Division of HIV/AIDS, National Institute for Infectious Diseases L. Spallanzani, IRCCS, Rome, Italy.

Annalisa Saracino (A)

Division of Infectious Diseases, University of Bari, Policlinic Hospital, Bari, Italy.

Giuseppe Lapadula (G)

Division of Infectious Diseases, 'San Gerardo' Hospital, Monza, Italy.

Stefano Rusconi (S)

Infectious Diseases Unit, DIBIC Luigi Sacco, University of Milan, Milan, Italy.

Francesco Castelli (F)

University Department of Infectious and Tropical Diseases, University of Brescia and Spedali Civili General Hospital, Brescia, Italy.

Simona Di Giambenedetto (S)

Infectious Diseases Unit, Catholic University of Sacred Heart, Rome, Italy.

Massimo Andreoni (M)

Clinical Infectious Diseases, University Hospital 'Tor Vergata', Rome, Italy.

Giovanni Di Perri (G)

Unit of Infectious Diseases, Department of Medical Sciences, University of Turin, Turin, Italy.

Andrea Antinori (A)

Clinical Division of HIV/AIDS, National Institute for Infectious Diseases L. Spallanzani, IRCCS, Rome, Italy.

Cristina Mussini (C)

Clinic of Infectious Diseases, University Hospital, University of Modena and Reggio Emilia, Modena, Italy.

Francesca Ceccherini-Silberstein (F)

Department of Experimental Medicine, University of Rome 'Tor Vergata', Rome, Italy.

Antonella D'Arminio Monforte (AD)

Department of Health Sciences, Clinic of Infectious Diseases, ASST Santi Paolo e Carlo, University of Milan, Milan, Italy.

Carlo F Perno (CF)

Virology Unit, National Institute for Infectious Diseases L. Spallanzani, IRCCS, Rome, Italy.
Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.

Maria M Santoro (MM)

Department of Experimental Medicine, University of Rome 'Tor Vergata', Rome, Italy.

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