Real-Life Experience on Dolutegravir and Lamivudine as Initial or Switch Therapy in a Silver Population Living with HIV.


Journal

Viruses
ISSN: 1999-4915
Titre abrégé: Viruses
Pays: Switzerland
ID NLM: 101509722

Informations de publication

Date de publication:
15 08 2023
Historique:
received: 19 07 2023
revised: 08 08 2023
accepted: 10 08 2023
medline: 28 8 2023
pubmed: 26 8 2023
entrez: 26 8 2023
Statut: epublish

Résumé

Clinical trials and real-life studies have granted the efficacy and safety of dolutegravir and lamivudine (DTG/3TC) in naïve and experienced people living with HIV (PLWH), but there are no long-term data in elderly people. We herein describe our real-life cohort of PLWH who were ≥65 years of age (PLWH ≥ 65) who started or were switched to DTG/3TC, single-tablet regimen, or DTG plus 3TC. We considered laboratory/clinical parameter changes from the baseline to the last follow-up time point available for each person by the paired Wilcoxon test and analyzed factors associated with virological failure (VF) and discontinuation. We included 112 PLWH with a median age of 66 (IQR: 65-70) years, 77.6% males; 84.8% of people had multimorbidity, 34.8% were on polypharmacy, and only 5.4% were naïve to treatment. Reasons to be switched to DTG/3TC were: abacavir removal (38.7%), treatment simplification (33.1%), and PI discontinuation (28.2%). The median treatment durability was 6 (IQR: 5.4-7) years. No significant changes were detected in metabolic, renal, immunological, or cardiovascular biomarkers during follow-up. HIV RNA undetectability was maintained in 104 (92.8%) individuals for whom follow-up evaluation was available. We observed eight discontinuations (two deaths, two VFs, two early intolerances, one significant weight gain, and one switch to long-acting therapy). No factors were significantly associated with VF or discontinuation. This is the first study on DTG/3TC in PLWH ≥ 65 with a follow-up longer than 5 years. DTG/3TC was found to be safe and effective, neutral on metabolic parameters, and with a low discontinuation rate for toxicity or VF.

Sections du résumé

BACKGROUND
Clinical trials and real-life studies have granted the efficacy and safety of dolutegravir and lamivudine (DTG/3TC) in naïve and experienced people living with HIV (PLWH), but there are no long-term data in elderly people. We herein describe our real-life cohort of PLWH who were ≥65 years of age (PLWH ≥ 65) who started or were switched to DTG/3TC, single-tablet regimen, or DTG plus 3TC.
METHODS
We considered laboratory/clinical parameter changes from the baseline to the last follow-up time point available for each person by the paired Wilcoxon test and analyzed factors associated with virological failure (VF) and discontinuation.
RESULTS
We included 112 PLWH with a median age of 66 (IQR: 65-70) years, 77.6% males; 84.8% of people had multimorbidity, 34.8% were on polypharmacy, and only 5.4% were naïve to treatment. Reasons to be switched to DTG/3TC were: abacavir removal (38.7%), treatment simplification (33.1%), and PI discontinuation (28.2%). The median treatment durability was 6 (IQR: 5.4-7) years. No significant changes were detected in metabolic, renal, immunological, or cardiovascular biomarkers during follow-up. HIV RNA undetectability was maintained in 104 (92.8%) individuals for whom follow-up evaluation was available. We observed eight discontinuations (two deaths, two VFs, two early intolerances, one significant weight gain, and one switch to long-acting therapy). No factors were significantly associated with VF or discontinuation.
CONCLUSIONS
This is the first study on DTG/3TC in PLWH ≥ 65 with a follow-up longer than 5 years. DTG/3TC was found to be safe and effective, neutral on metabolic parameters, and with a low discontinuation rate for toxicity or VF.

Identifiants

pubmed: 37632082
pii: v15081740
doi: 10.3390/v15081740
pmc: PMC10459453
pii:
doi:

Substances chimiques

dolutegravir DKO1W9H7M1
Lamivudine 2T8Q726O95
Silver 3M4G523W1G
Heterocyclic Compounds, 3-Ring 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Maria Mazzitelli (M)

Infectious and Tropical Diseases Unit, Padua University Hospital, 35128 Padua, Italy.

Lolita Sasset (L)

Infectious and Tropical Diseases Unit, Padua University Hospital, 35128 Padua, Italy.

Samuele Gardin (S)

Infectious and Tropical Diseases Unit, Padua University Hospital, 35128 Padua, Italy.

Davide Leoni (D)

Infectious and Tropical Diseases Unit, Padua University Hospital, 35128 Padua, Italy.

Mattia Trunfio (M)

Infectious Diseases Unit, Department of Medical Sciences, University of Turin, Amedeo di Savoia Hospital, 10149 Turin, Italy.
HIV Neurobehavioral Research Program, Departments of Neurosciences and Psychiatry, School of Medicine, University of California, San Diego, CA 92093, USA.

Vincenzo Scaglione (V)

Infectious and Tropical Diseases Unit, Padua University Hospital, 35128 Padua, Italy.

Daniele Mengato (D)

Hospital Pharmacy Unit, Padua University Hospital, 35128 Padua, Italy.

Elena Agostini (E)

Infectious and Tropical Diseases Unit, Padua University Hospital, 35128 Padua, Italy.

Eleonora Vania (E)

Infectious and Tropical Diseases Unit, Padua University Hospital, 35128 Padua, Italy.
Infectious Disease Unit, Department of Medicine, University of Udine, 33100 Udine, Italy.

Cristina Putaggio (C)

Infectious and Tropical Diseases Unit, Padua University Hospital, 35128 Padua, Italy.

Annamaria Cattelan (A)

Infectious and Tropical Diseases Unit, Padua University Hospital, 35128 Padua, Italy.
Department of Molecular Medicine, University of Padua, 35131 Padua, Italy.

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