Role of interferon therapy in severe COVID-19: the COVIFERON randomized controlled trial.
Aged
Aged, 80 and over
Antiviral Agents
/ therapeutic use
COVID-19
/ virology
Female
Humans
Interferon beta-1a
/ therapeutic use
Interferon beta-1b
/ therapeutic use
Male
Middle Aged
RNA, Viral
/ analysis
Real-Time Polymerase Chain Reaction
SARS-CoV-2
/ genetics
Thorax
/ diagnostic imaging
Treatment Outcome
COVID-19 Drug Treatment
Journal
Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288
Informations de publication
Date de publication:
13 04 2021
13 04 2021
Historique:
received:
27
07
2020
accepted:
17
03
2021
entrez:
14
4
2021
pubmed:
15
4
2021
medline:
22
4
2021
Statut:
epublish
Résumé
Type 1 Interferons (IFNs) have been associated with positive effects on Coronaviruses. Previous studies point towards the superior potency of IFNβ compared to IFNα against viral infections. We conducted a three-armed, individually-randomized, open-label, controlled trial of IFNβ1a and IFNβ1b, comparing them against each other and a control group. Patients were randomly assigned in a 1:1:1 ratio to IFNβ1a (subcutaneous injections of 12,000 IU on days 1, 3, 6), IFNβ1b (subcutaneous injections of 8,000,000 IU on days 1, 3, 6), or the control group. All three arms orally received Lopinavir/Ritonavir (400 mg/100 mg twice a day for ten days) and a single dose of Hydroxychloroquine 400 mg on the first day. Our utilized primary outcome measure was Time To Clinical Improvement (TTCI) defined as the time from enrollment to discharge or a decline of two steps on the clinical seven-step ordinal scale, whichsoever came first. A total of 60 severely ill patients with positive RT-PCR and Chest CT scans underwent randomization (20 patients to each arm). In the Intention-To-Treat population, IFNβ1a was associated with a significant difference against the control group, in the TTCI; (HR; 2.36, 95% CI 1.10-5.17, P-value = 0.031) while the IFNβ1b indicated no significant difference compared with the control; HR; 1.42, (95% CI 0.63-3.16, P-value = 0.395). The median TTCI for both of the intervention groups was five days vs. seven days for the control group. The mortality was numerically lower in both of the intervention groups (20% in the IFNβ1a group and 30% in the IFNβ1b group vs. 45% in the control group). There were no significant differences between the three arms regarding the adverse events. In patients with laboratory-confirmed SARS-CoV-2 infection, as compared with the base therapeutic regiment, the benefit of a significant reduction in TTCI was observed in the IFNβ1a arm. This finding needs further confirmation in larger studies.Trial Registration Number: ClinicalTrials.gov, NCT04343768. (Submitted: 08/04/2020; First Online: 13/04/2020) (Registration Number: NCT04343768).
Identifiants
pubmed: 33850184
doi: 10.1038/s41598-021-86859-y
pii: 10.1038/s41598-021-86859-y
pmc: PMC8044200
doi:
Substances chimiques
Antiviral Agents
0
RNA, Viral
0
Interferon beta-1b
145155-23-3
Interferon beta-1a
XRO4566Q4R
Banques de données
ClinicalTrials.gov
['NCT04343768']
Types de publication
Journal Article
Randomized Controlled Trial
Langues
eng
Sous-ensembles de citation
IM
Pagination
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