Dolutegravir Monotherapy Versus Dolutegravir/Abacavir/Lamivudine for Virologically Suppressed People Living With Chronic Human Immunodeficiency Virus Infection: The Randomized Noninferiority MONotherapy of TiviCAY Trial.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
15 10 2019
Historique:
received: 01 10 2018
accepted: 29 12 2018
pubmed: 3 1 2019
medline: 15 9 2020
entrez: 3 1 2019
Statut: ppublish

Résumé

We investigated whether dolutegravir (DTG) monotherapy could be used to maintain virological suppression in people living with human immunodeficiency virus (HIV) on a successful dolutegravir-based triple therapy. MONCAY (MONotherapy of TiviCAY) was a 48-week, multicentric, randomized, open-label, 12% noninferiority margin trial. Patients with CD4 nadir >100/μL, plasma HIV-1 RNA <50 copies/mL for ≥12 months, and stable regimen with DTG/abacavir (ABC)/lamivudine (3TC) were 1:1 randomized to continue their regimen or to DTG monotherapy. The primary endpoint was the proportion of patients with HIV RNA <50 copies/mL at week 24 in intention-to-treat snapshot analysis. Virologic failure (VF) was defined as 2 consecutive HIV RNA >50 copies/mL within 2 weeks apart. Seventy-eight patients were assigned to DTG monotherapy and 80 to continue DTG/ABC/3TC. By week 24, 2 patients in the DTG group experienced VF without resistance to the integrase strand transfer inhibitor (INSTI) class; 1 patient discontinued DTG/ABC/3TC due to an adverse event. The success rate at week 24 was 73/78 (93.6%) in the DTG arm and 77/80 (96.3%) in the DTG/ABC/3TC arm (difference, 2.7%; 95% confidence interval [CI], -5.0 to 10.8). During subsequent follow-up, 5 additional VFs occurred in the DTG arm (2 of which harbored emerging resistance mutation to INSTI). The cumulative incidence of VF at week 48 was 9.7% (95% CI, 2.8 to 16.6) in the DTG arm compared with 0% in the DTG/ABC/3TC arm (P = .005 by the log-rank test). The Data Safety Monitoring Board recommended to reintensify the DTG arm with standardized triple therapy. Because the risk of VF with resistance increases over time, we recommend avoiding DTG monotherapy as a maintenance strategy among people living with chronic HIV infection. NCT02596334 and EudraCT 2015-002853-36.

Sections du résumé

BACKGROUND
We investigated whether dolutegravir (DTG) monotherapy could be used to maintain virological suppression in people living with human immunodeficiency virus (HIV) on a successful dolutegravir-based triple therapy.
METHODS
MONCAY (MONotherapy of TiviCAY) was a 48-week, multicentric, randomized, open-label, 12% noninferiority margin trial. Patients with CD4 nadir >100/μL, plasma HIV-1 RNA <50 copies/mL for ≥12 months, and stable regimen with DTG/abacavir (ABC)/lamivudine (3TC) were 1:1 randomized to continue their regimen or to DTG monotherapy. The primary endpoint was the proportion of patients with HIV RNA <50 copies/mL at week 24 in intention-to-treat snapshot analysis. Virologic failure (VF) was defined as 2 consecutive HIV RNA >50 copies/mL within 2 weeks apart.
RESULTS
Seventy-eight patients were assigned to DTG monotherapy and 80 to continue DTG/ABC/3TC. By week 24, 2 patients in the DTG group experienced VF without resistance to the integrase strand transfer inhibitor (INSTI) class; 1 patient discontinued DTG/ABC/3TC due to an adverse event. The success rate at week 24 was 73/78 (93.6%) in the DTG arm and 77/80 (96.3%) in the DTG/ABC/3TC arm (difference, 2.7%; 95% confidence interval [CI], -5.0 to 10.8). During subsequent follow-up, 5 additional VFs occurred in the DTG arm (2 of which harbored emerging resistance mutation to INSTI). The cumulative incidence of VF at week 48 was 9.7% (95% CI, 2.8 to 16.6) in the DTG arm compared with 0% in the DTG/ABC/3TC arm (P = .005 by the log-rank test). The Data Safety Monitoring Board recommended to reintensify the DTG arm with standardized triple therapy.
CONCLUSIONS
Because the risk of VF with resistance increases over time, we recommend avoiding DTG monotherapy as a maintenance strategy among people living with chronic HIV infection.
CLINICAL TRIALS REGISTRATION
NCT02596334 and EudraCT 2015-002853-36.

Identifiants

pubmed: 30601976
pii: 5269432
doi: 10.1093/cid/ciy1132
doi:

Substances chimiques

Anti-HIV Agents 0
Dideoxynucleosides 0
Heterocyclic Compounds, 3-Ring 0
Oxazines 0
Piperazines 0
Pyridones 0
Lamivudine 2T8Q726O95
dolutegravir DKO1W9H7M1
abacavir WR2TIP26VS

Banques de données

ClinicalTrials.gov
['NCT02596334']
EudraCT
['2015-002853-36']

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1498-1505

Investigateurs

Olivier Bollengier-Stragier (O)
Jean-Luc Esnault (JL)
Thomas Guimard (T)
Sophie Leautez (S)
Philippe Perré (P)
Romain Lemarie (R)
Xavier Pouget-Abadie (X)
Mariam Roncato-Saberan (M)
Marie André (M)
Thierry May (T)
Evelyne Schvoerer (E)
Clotilde Allavena (C)
Elisabeth Andre-Garnier (E)
Camille Bernaud (C)
Eric Billaud (E)
Sabelline Bouchez (S)
Nolwenn Hall (N)
François Raffi (F)
Véronique Reliquet (V)
Florian Vivrel (F)
Pascale Deleplanque (P)
Anabele Dos-Santos (A)
Simon Sunder (S)
Cendrine Boulard (C)
Aurélie Despujols (A)
Jérôme Guinard (J)
Laurent Hocqueloux (L)
Sandrine Lefeuvre (S)
Catherine Mille (C)
Mohamadou Niang (M)
Montasser Ouezzani (M)
Thierry Prazuck (T)
Gaëlle Thomas (G)
Antoine Valéry (A)
Véronique Avettand-Fènoël (V)
Geneviève Giraudeau (G)
Gwenaël Le Moal (G)
Marie-Laure Batard (ML)
Samira Fafi-Kremer (S)
David Rey (D)
Francis Barin (F)
Frédéric Bastides (F)
Louis Bernard (L)
Guillaume Gras (G)
Marie Charlotte Hallouin-Bernard (MC)
Adrien Lemaignen (A)
Pascal Le Bret (P)
Karl Stefic (K)

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

Auteurs

Laurent Hocqueloux (L)

Service des Maladies Infectieuses et Tropicales, CHR d'Orléans-La Source, Tours.

François Raffi (F)

Service des Maladies Infectieuses, CHU Hôtel Dieu and INSERM UIC 1413 Nantes University, Tours.

Thierry Prazuck (T)

Service des Maladies Infectieuses et Tropicales, CHR d'Orléans-La Source, Tours.

Louis Bernard (L)

Service des Maladies Infectieuses, CHU Bretonneau, Tours.

Simon Sunder (S)

Service des Maladies Infectieuses et Tropicales, CHG de Niort.

Jean-Luc Esnault (JL)

Service des Maladies Infectieuses, CHD de Vendée, La Roche-sur-Yon.

David Rey (D)

Le Trait d'Union, Hôpitaux Universitaires de Strasbourg.

Gwenaël Le Moal (G)

Service des Maladies Infectieuses, CHU La Milétrie, Poitiers.

Mariam Roncato-Saberan (M)

Service des Maladies Infectieuses, Groupe Hospitalier de La Rochelle-Ré-Aunis, Nancy.

Marie André (M)

Service des Maladies Infectieuses, CHRU-Brabois, Nancy.

Eric Billaud (E)

Service des Maladies Infectieuses, CHU Hôtel Dieu and INSERM UIC 1413 Nantes University, Tours.

Antoine Valéry (A)

Département d'Informatique Médicale, CHR d'Orléans-La Source, France.

Véronique Avettand-Fènoël (V)

Laboratoire de Microbiologie clinique, CHU Necker and Université Paris Descartes, Sorbonne Paris Cité.

Jean-Jacques Parienti (JJ)

Unité de Biostatistique et de Recherche Clinique, CHU de Caen; EA2656 Groupe de Recherche sur l'Adaptation Microbienne (GRAM 2.0), Université Caen Normandie, Caen, France.

Clotilde Allavena (C)

Service des Maladies Infectieuses, CHU Hôtel Dieu and INSERM UIC 1413 Nantes University, Tours.

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