A meta-analysis of clinical studies conducted during the West Africa Ebola virus disease outbreak confirms the need for randomized control groups.


Journal

Science translational medicine
ISSN: 1946-6242
Titre abrégé: Sci Transl Med
Pays: United States
ID NLM: 101505086

Informations de publication

Date de publication:
27 11 2019
Historique:
received: 03 12 2018
accepted: 04 07 2019
entrez: 29 11 2019
pubmed: 30 11 2019
medline: 12 9 2020
Statut: ppublish

Résumé

Recent Ebola virus disease outbreaks affirm the dire need for treatments with proven efficacy. Randomized controlled clinical trials remain the gold standard but, during disease outbreaks, may be difficult to conduct due to ethical concerns and challenging field conditions. In the absence of a randomized control group, statistical modeling to create a control group could be a possibility. Such a model-based reference control would only be credible if it had the same mortality risk as that of the experimental group in the absence of treatment. One way to test this counterfactual assumption is to evaluate whether reasonable similarity exists across nonrandomized control groups from different clinical studies, which might suggest that a future control group would be similarly homogeneous. We evaluated similarity across six clinical studies conducted during the 2013-2016 West Africa outbreak of Ebola virus disease. These studies evaluated favipiravir, the biologic ZMapp, the antimalarial drug amodiaquine, or administration of convalescent plasma or convalescent whole blood. We compared the nonrandomized control groups of these six studies comprising 1147 individuals infected with Ebola virus. We found considerable heterogeneity, which did not disappear after statistical modeling to adjust for prognostic variables. Mortality risk varied widely (31 to 66%) across the nonrandomized control arms of these six studies. Models adjusting for baseline covariates (age, sex, and cycle threshold, a proxy for viral load) failed to sufficiently recalibrate these studies and showed that heterogeneity remained. Our findings highlight concerns about making invalid conclusions when comparing nonrandomized control groups to cohorts receiving experimental treatments.

Identifiants

pubmed: 31776287
pii: 11/520/eaaw1049
doi: 10.1126/scitranslmed.aaw1049
pii:
doi:

Substances chimiques

Drugs, Investigational 0

Types de publication

Journal Article Meta-Analysis Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NCI NIH HHS
ID : HHSN261200800001E
Pays : United States

Informations de copyright

Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.

Auteurs

Lori E Dodd (LE)

Biostatistics Research Branch, Division of Clinical Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA. doddl@mail.nih.gov.
School of Public Health and Family Medicine, University of Cape Town, Cape Town, South Africa.

Dean Follmann (D)

Biostatistics Research Branch, Division of Clinical Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.

Michael Proschan (M)

Biostatistics Research Branch, Division of Clinical Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.

Jing Wang (J)

Clinical Monitoring Research Program Directorate, Frederick National Laboratory for Cancer Research Sponsored by the National Cancer Institute, Frederick, MD, USA.

Denis Malvy (D)

Inserm, UMR 1219, Université de Bordeaux, Bordeaux, France.
Centre Hospitalier Universitaire de Bordeaux, Bordeaux, France.

Johan van Griensven (J)

Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.

Iza Ciglenecki (I)

Operational Centre Geneva, Médecins Sans Frontières, 1211 Geneva, Switzerland.

Peter W Horby (PW)

Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, UK.

Rashid Ansumana (R)

Mercy Hospital Research Laboratory, Kulanda Town, Bo, Sierra Leone.
School of Community Health Sciences, Njala University, Bo, Sierra Leone.

Jia-Fu Jiang (JF)

Beijing Institute of Microbiology and Epidemiology, Beijing, China.

Richard T Davey (RT)

Laboratory of Immunoregulation, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.

H Clifford Lane (HC)

Division of Clinical Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.

Aurelie Gouel-Cheron (A)

Biostatistics Research Branch, Division of Clinical Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
Anesthesiology and Intensive Care Department, Hopital Bichat-Claude Bernard, Assistance Publique-Hopitaux de Paris, Paris, France.

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