Systematic Review and Meta-analysis of Treatment Interruptions in Human Immunodeficiency Virus (HIV) Type 1-infected Patients Receiving Antiretroviral Therapy: Implications for Future HIV Cure Trials.


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:
17 03 2020
Historique:
received: 21 11 2018
accepted: 17 05 2019
pubmed: 19 5 2019
medline: 7 1 2021
entrez: 19 5 2019
Statut: ppublish

Résumé

Safety and tolerability of analytical treatment interruptions (ATIs) as a vital part of human immunodeficiency virus type 1 (HIV-1) cure studies are discussed. We analyzed current evidence for the occurrence of adverse events (AEs) during TIs. Our analysis included studies that reported on AEs in HIV-1-infected patients undergoing TIs. All interventional and observational studies were reviewed, and results were extracted based on predefined criteria. The proportion of AEs was pooled using random-effects models. Metaregression was used to explore the influence of baseline CD4+ T-cell count, viral load, study type, previous time on combined antiretroviral therapy, and follow-up interval during TIs. We identified 1048 studies, of which 22 studies including 7104 individuals fulfilled the defined selection criteria. Included studies had sample sizes between 6 and 5472 participants, with durations of TI cycles ranging from 7 days to 27 months. The intervals of HIV-1-RNA testing varied from 2 days to 3 months during TIs. The overall proportion of AEs during TIs >4 weeks was 3% (95% confidence interval [CI], 0%-7%) and was lower in studies with follow-up intervals ≤14 days (0%; 95% CI, 0%-1%) than in studies with wider follow-up intervals (6%; 95% CI, 2%-13%; P value for interaction = .01). We found moderate-quality evidence indicating that studies with narrow follow-up intervals did not show a substantial increase in AEs during TIs. Our findings indicate that ATI may be a safe strategy as part of HIV-1 cure trials by closely monitoring for HIV-1 rebound.

Sections du résumé

BACKGROUND
Safety and tolerability of analytical treatment interruptions (ATIs) as a vital part of human immunodeficiency virus type 1 (HIV-1) cure studies are discussed. We analyzed current evidence for the occurrence of adverse events (AEs) during TIs.
METHODS
Our analysis included studies that reported on AEs in HIV-1-infected patients undergoing TIs. All interventional and observational studies were reviewed, and results were extracted based on predefined criteria. The proportion of AEs was pooled using random-effects models. Metaregression was used to explore the influence of baseline CD4+ T-cell count, viral load, study type, previous time on combined antiretroviral therapy, and follow-up interval during TIs.
RESULTS
We identified 1048 studies, of which 22 studies including 7104 individuals fulfilled the defined selection criteria. Included studies had sample sizes between 6 and 5472 participants, with durations of TI cycles ranging from 7 days to 27 months. The intervals of HIV-1-RNA testing varied from 2 days to 3 months during TIs. The overall proportion of AEs during TIs >4 weeks was 3% (95% confidence interval [CI], 0%-7%) and was lower in studies with follow-up intervals ≤14 days (0%; 95% CI, 0%-1%) than in studies with wider follow-up intervals (6%; 95% CI, 2%-13%; P value for interaction = .01).
CONCLUSIONS
We found moderate-quality evidence indicating that studies with narrow follow-up intervals did not show a substantial increase in AEs during TIs. Our findings indicate that ATI may be a safe strategy as part of HIV-1 cure trials by closely monitoring for HIV-1 rebound.

Identifiants

pubmed: 31102444
pii: 5491629
doi: 10.1093/cid/ciz417
doi:

Substances chimiques

Anti-Retroviral Agents 0

Types de publication

Journal Article Meta-Analysis Research Support, Non-U.S. Gov't Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1406-1417

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

Melanie Stecher (M)

Department I for Internal Medicine, University Hospital of Cologne.
German Center for Infection Research, Partner Site Bonn-Cologne.

Annika Claßen (A)

Department I for Internal Medicine, University Hospital of Cologne.
German Center for Infection Research, Partner Site Bonn-Cologne.

Florian Klein (F)

German Center for Infection Research, Partner Site Bonn-Cologne.
Laboratory of Experimental Immunology, Institute of Virology.
Center for Molecular Medicine Cologne, University of Cologne.

Clara Lehmann (C)

Department I for Internal Medicine, University Hospital of Cologne.
German Center for Infection Research, Partner Site Bonn-Cologne.

Henning Gruell (H)

Department I for Internal Medicine, University Hospital of Cologne.
German Center for Infection Research, Partner Site Bonn-Cologne.
Laboratory of Experimental Immunology, Institute of Virology.

Martin Platten (M)

Labor Dr. Wisplinghoff, Cologne.

Christoph Wyen (C)

Department I for Internal Medicine, University Hospital of Cologne.
Praxis am Ebertplatz, Cologne.

Georg Behrens (G)

Department for Clinical Immunology and Rheumatology Hannover Medical School.
German Center for Infection Research, Partner Site Hannover.

Gerd Fätkenheuer (G)

Department I for Internal Medicine, University Hospital of Cologne.
German Center for Infection Research, Partner Site Bonn-Cologne.

Jörg Janne Vehreschild (JJ)

Department I for Internal Medicine, University Hospital of Cologne.
German Center for Infection Research, Partner Site Bonn-Cologne.
Medical Department II, University Hospital of Frankfurt, Germany.

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Classifications MeSH