The current spread of the COrona VIrus Disease-2019 (COVID-19) epidemic in Italy, and the current lack of effective and approved drugs for its treatment, poses the problem of Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infected patients management, especially those who underwent to experience COVID-19 complications, such as CRS. This unmet need becomes more severe if the investigator consider that, the COVID-19 mortality stands around 2% in the general population, but it rises to 49% when considering intensive care unit (ICU) patients. To increase the chances of survival of these patients, the compassionate use of the available drugs is required, based on literature data, to the best of our abilities. ICU patients with cytokine release syndrome (CRS) secondary to COVID-19, show increased production of pro-inflammatory cytokines, including interleukin (IL-6), IL-2, IL-7, IL-10, tumor necrosis factor (TNF)-α and interferon (INF)γ, similar to that found in patients who develop CRS secondary to Chimeric Antigen Receptor-T (CAR-T) therapy. Although immuno-modulatory therapy is not routinely recommended in COVID-19 pneumonia, tocilizumab might have a rationale in those patients who develop CRS, blocking the complications caused by high levels of IL-6, and possibly preventing the development of a multi-organ failure. Reassuring data in this sense, come from the first studies conducted in China. In a Chinese pilot study, Xiaoling Xu and collaborators used tocilizumab (at a dosage of 400 mg iv in a single dose, with a possible second dose in case of no clinical response) in patients with COVID-19 in the presence of one of the following criteria: i) respiratory rate ≥ 30 acts/min; ii) SpO2 ≤ 93% in ambient air; iii) PaO2/FiO2 ≤ 300 mmHg. In the 21 patients treated with tocilizumab a significant reduction in IL-6 levels and fever, with improvement in lung function, was demonstrated. Besides, 90% of treated patients showed an improvement in the radiological picture, in terms of a decrease in the frosted glass areas, and a return to normal lymphocytes count in the peripheral blood. This is a prospective observational clinical study and it is aimed at verifying tocilizumab efficacy and safety in patients with COVID-19 complicated by acute distress respiratory syndrome (ARDS) and CRS.
Study Type
OBSERVATIONAL
Enrollment
30
Ospedale San Salvatore
L’Aquila, Italy
RECRUITINGPercentage of patients with complete recovery defined as fever disappearance and return to normal peripheral oxygen saturation values (SpO2) after 14 days from the end of treatment with tocilizumab.
Fever normalization criteria: Temperature \<36.6 ° C for at least 72 hours; SpO2 normalization criterion: SpO2\> 94% for at least 72 hours
Time frame: 14 days
Percentage of patients achieving a score <3 on the Brescia-COVID respiratory severity scale (BCRSS) after the last tocilizumab administration.
Time frame: 24 hours
Percentage of patients with partial recovery defined as the disappearance of fever 14 days after the end of treatment with tocilizumab.
Fever normalization criteria: Temperature \<36.6 ° C for at least 72 hours
Time frame: 14 days
Duration of hospitalization
days
Time frame: 14 days
Time to the first negative SARS-CoV-2 negative RT-PCR test
days
Time frame: 14 days
Changes from the baseline in the white blood cell count
number/microliter
Time frame: 7, 14 days
Changes from the baseline in the lymphocyte populations (cluster of differentiation (CD)3+CD4+, CD3+CD8+, CD19+, Th17)
number/microliter
Time frame: 7, 14 days
Changes from the baseline of c-reactive protein (CRP) values
Time frame: 7, 14 days
Changes from the baseline of Ferritin values
Time frame: 7, 14 days
Changes from the baseline of BNP values
Time frame: 7,14 days
Changes from the baseline of CK-MB values
Time frame: 7,14 days
Changes from the baseline of Troponin values
Time frame: 7,14 days
Changes from the baseline of LDH values
Time frame: 7,14 days
Changes from the baseline of myoglobulin values
Time frame: 7,14 days
Changes in myocardial ischemia signs at the electrocardiographic trace (YES or NO)
(ST segments elevation or depression, T-wave changes)
Time frame: 7,14 days
Rate of adverse events report during and after tocilizumab
Time frame: 14 days
Mortality (number of Partecipants, cause and timing)
Time frame: 12 weeks
Percentage of patients who develop autoimmune diseases
Time frame: 1 year
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