Subcutaneous tocilizumab treatment in patients with severe COVID-19-related cytokine release syndrome: An observational cohort study.

Coronavirus disease 2019 Cytokine release syndrome Tocilizumab

Journal

EClinicalMedicine
ISSN: 2589-5370
Titre abrégé: EClinicalMedicine
Pays: England
ID NLM: 101733727

Informations de publication

Date de publication:
Jul 2020
Historique:
received: 09 04 2020
revised: 21 05 2020
accepted: 21 05 2020
entrez: 9 8 2020
pubmed: 9 8 2020
medline: 9 8 2020
Statut: epublish

Résumé

Patients with severe coronavirus disease 2019 (COVID-19) have elevated levels of acute phase reactants and inflammatory cytokines, including interleukin-6, indicative of cytokine release syndrome (CRS). The interleukin-6 receptor inhibitor tocilizumab is used for the treatment of chimeric antigen receptor T-cell therapy-induced CRS. Patients aged 18 years or older with laboratory-confirmed COVID-19 admitted to the Annunziata Hospital in Cosenza, Italy, through March 7, 2020, who received at least one dose of tocilizumab 162 mg subcutaneously for the treatment of COVID-19-related CRS in addition to standard care were included in this retrospective observational study. The primary observation was the incidence of grade 4 CRS after tocilizumab treatment. Chest computed tomography (CT) scans were evaluated to investigate lung manifestations. Twelve patients were included; all had fever, cough, and fatigue at presentation, and all had at least one comorbidity (hypertension, six patients; diabetes, five patients; chronic obstructive lung disease, four patients). Seven patients received high-flow nasal cannula oxygen therapy and five received non-invasive mechanical ventilation for lung complications of COVID-19. No incidence of grade 4 CRS was observed within 1 week of tocilizumab administration in all 12 patients (100%) and within 2 days of tocilizumab administration in 5 patients (42%). The predominant pattern on chest CT scans at presentation was ground-glass opacity, air bronchograms, smooth or irregular interlobular or septal thickening, and thickening of the adjacent pleura. Follow-up CT scans 7 to 10 days after tocilizumab treatment showed improvement of lung manifestations in all patients. No adverse events or new safety concerns attributable to tocilizumab were reported. Tocilizumab administered subcutaneously to patients with COVID-19 and CRS is a promising treatment for reduction in disease activity and improvement in lung function. The effect of tocilizumab should be confirmed in a randomised controlled trial.

Sections du résumé

BACKGROUND BACKGROUND
Patients with severe coronavirus disease 2019 (COVID-19) have elevated levels of acute phase reactants and inflammatory cytokines, including interleukin-6, indicative of cytokine release syndrome (CRS). The interleukin-6 receptor inhibitor tocilizumab is used for the treatment of chimeric antigen receptor T-cell therapy-induced CRS.
METHODS METHODS
Patients aged 18 years or older with laboratory-confirmed COVID-19 admitted to the Annunziata Hospital in Cosenza, Italy, through March 7, 2020, who received at least one dose of tocilizumab 162 mg subcutaneously for the treatment of COVID-19-related CRS in addition to standard care were included in this retrospective observational study. The primary observation was the incidence of grade 4 CRS after tocilizumab treatment. Chest computed tomography (CT) scans were evaluated to investigate lung manifestations.
FINDINGS RESULTS
Twelve patients were included; all had fever, cough, and fatigue at presentation, and all had at least one comorbidity (hypertension, six patients; diabetes, five patients; chronic obstructive lung disease, four patients). Seven patients received high-flow nasal cannula oxygen therapy and five received non-invasive mechanical ventilation for lung complications of COVID-19. No incidence of grade 4 CRS was observed within 1 week of tocilizumab administration in all 12 patients (100%) and within 2 days of tocilizumab administration in 5 patients (42%). The predominant pattern on chest CT scans at presentation was ground-glass opacity, air bronchograms, smooth or irregular interlobular or septal thickening, and thickening of the adjacent pleura. Follow-up CT scans 7 to 10 days after tocilizumab treatment showed improvement of lung manifestations in all patients. No adverse events or new safety concerns attributable to tocilizumab were reported.
INTERPRETATION CONCLUSIONS
Tocilizumab administered subcutaneously to patients with COVID-19 and CRS is a promising treatment for reduction in disease activity and improvement in lung function. The effect of tocilizumab should be confirmed in a randomised controlled trial.

Identifiants

pubmed: 32766535
doi: 10.1016/j.eclinm.2020.100410
pii: S2589-5370(20)30154-1
pii: 100410
pmc: PMC7329292
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100410

Informations de copyright

© 2020 The Author(s).

Déclaration de conflit d'intérêts

The authors have no conflicts of interest to disclose.

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Auteurs

Antonio Mastroianni (A)

Infectious Diseases Unit, Annunziata Hospital, Viale della Repubblica s.n.c., 87100 Cosenza, Italy.

Sonia Greco (S)

Infectious Diseases Unit, Annunziata Hospital, Viale della Repubblica s.n.c., 87100 Cosenza, Italy.

Giovanni Apuzzo (G)

Infectious Diseases Unit, Annunziata Hospital, Viale della Repubblica s.n.c., 87100 Cosenza, Italy.

Salvatore De Santis (S)

Infectious Diseases Unit, Annunziata Hospital, Viale della Repubblica s.n.c., 87100 Cosenza, Italy.

Carmela Oriolo (C)

Hospital Pharmacy, Annunziata Hospital, Cosenza, Italy.

Alfredo Zanolini (A)

Radiology Unit, Annunziata Hospital, Cosenza, Italy.

Luciana Chidichimo (L)

Infectious Diseases Unit, Annunziata Hospital, Viale della Repubblica s.n.c., 87100 Cosenza, Italy.

Valeria Vangeli (V)

Infectious Diseases Unit, Annunziata Hospital, Viale della Repubblica s.n.c., 87100 Cosenza, Italy.

Classifications MeSH