Efficacy and Safety of Tocilizumab in the Treatment of SARS-Cov-2 Related Pneumonia
- Conditions
- COVID-19 Pneumonia
- Registration Number
- NCT04332913
- Lead Sponsor
- University of L'Aquila
- Brief Summary
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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 30
- All gender patients aged ≥ 18 years;
- Patients with SARS-CoV-2 infection confirmed by tests (RT-PCR) and pulmonary involvement, hospitalized, at the end of the initial phase of high viral load of COVID-19 (apyretic> 72 hours and / or at least 7 days after onset of symptoms);
- Worsening of respiratory exchanges such as to require non-invasive or invasive ventilation support (BCRSS score ≥ 3).
- High levels of IL-6 (> 40 pg/mL) or alternatively CRP and/or ferritin and/or D-dimer and/or fibrinogen values higher than the reference values or rapidly increasing;
- Signature of informed consent.
- Alanine aminotransferase and/or Aspartate aminotransferase (ALT / AST) > 5 times compared to normal laboratory values.
- Presence of a chronic renal failure ≥ 4 stage (glomerular filtrate values <30 ml/min/1.73 m2).
- Presence of neutropenia (neutrophils count < 500 / mm3).
- Platelet count less than 50 x 103/μL.
- Documented sepsis from other pathogens other than SARS-CoV-2.
- Presence of co-morbidities associated, in clinical judgment, with an unfavourable outcome.
- Complicated diverticulitis and / or intestinal perforation.
- Skin infection in progress (e.g. dermohypodermitis not controlled by antibiotic therapy).
- Immuno-suppressive anti-rejection therapy.
- Pregnancy or woman of childbearing age who does not use contraceptive and/or breastfeeding measures.
- Previous ischemic attack or myocardial infarction.
- NYHA class III or IV heart failure.
- Severe depressive syndrome or other psychiatric disease which, in the opinion of the doctor, can preclude patient participation in the study.
- Presence of known malignant neoplasms.
- Clinically significant history of alcohol abuse or drug addiction which, in the opinion of the doctor, may preclude the subject's participation in the study.
- Any condition which, in the opinion of the doctor, precludes the possibility of using the study drug provided for in the RCP.
- Any other laboratory condition or parameter that, in the doctor's judgment, precludes the subject's participation in the study.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Percentage 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. 14 days Fever normalization criteria: Temperature \<36.6 ° C for at least 72 hours; SpO2 normalization criterion: SpO2\> 94% for at least 72 hours
- Secondary Outcome Measures
Name Time Method Changes from the baseline of BNP values 7,14 days Percentage of patients achieving a score <3 on the Brescia-COVID respiratory severity scale (BCRSS) after the last tocilizumab administration. 24 hours Changes from the baseline in the white blood cell count 7, 14 days number/microliter
Changes from the baseline of myoglobulin values 7,14 days Changes in myocardial ischemia signs at the electrocardiographic trace (YES or NO) 7,14 days (ST segments elevation or depression, T-wave changes)
Rate of adverse events report during and after tocilizumab 14 days Percentage of patients with partial recovery defined as the disappearance of fever 14 days after the end of treatment with tocilizumab. 14 days Fever normalization criteria: Temperature \<36.6 ° C for at least 72 hours
Changes from the baseline of CK-MB values 7,14 days Changes from the baseline of LDH values 7,14 days Changes from the baseline of c-reactive protein (CRP) values 7, 14 days Time to the first negative SARS-CoV-2 negative RT-PCR test 14 days days
Changes from the baseline of Troponin values 7,14 days Mortality (number of Partecipants, cause and timing) 12 weeks Duration of hospitalization 14 days days
Changes from the baseline in the lymphocyte populations (cluster of differentiation (CD)3+CD4+, CD3+CD8+, CD19+, Th17) 7, 14 days number/microliter
Changes from the baseline of Ferritin values 7, 14 days Percentage of patients who develop autoimmune diseases 1 year
Trial Locations
- Locations (1)
Ospedale San Salvatore
🇮🇹L'Aquila, Italy