COVIDOSE: Low-dose tocilizumab in the treatment of Covid-19.
Garth W StrohbehnBrian L HeissSherin Juliet RouhaniJonathan A TrujilloJovian YuAlec J KacewEmily F HiggsJeffrey C BloodworthAlexandra CabanovRachel C WrightAdriana KoziolAlexandra WeissKeith DanaheyTheodore G KarrisonCuoghi C EdensIazsmin Bauer VenturaNatasha N PettitBhakti PatelJennifer PisanoMary E StrekThomas F GajewskiMark J RatainPankti D ReidPublished in: medRxiv : the preprint server for health sciences (2020)
Background Interleukin-6 (IL-6)-mediated hyperinflammation may contribute to the high mortality of coronavirus disease 2019 (Covid-19). Tocilizumab, an IL-6 receptor blocking monoclonal antibody, has been repurposed for Covid-19, but prospective trials and dose-finding studies in Covid-19 are lacking. Methods We conducted a phase 2 trial of low-dose tocilizumab in hospitalized adult patients with Covid-19, radiographic pulmonary infiltrate, fever, and C-reactive protein (CRP) >= 40 mg/L who did not require mechanical ventilation. Dose cohorts were determined by a trial Operations Committee, stratified by CRP and epidemiologic risk factors. A range of doses from 40 to 200 mg (low-dose tocilizumab) was evaluated, with allowance for one repeat dose at 24-48 hours. The primary objective was to assess the relationship of dose to fever resolution and CRP response. Outcomes were compared with retrospective controls with Covid-19. Correlative studies evaluating host antibody response were performed in parallel. Findings A total of 32 patients received low-dose tocilizumab. This cohort had improved fever resolution (75.0% vs. 34.2%, p = 0.001) and CRP decline (86.2% vs. 14.3%, p < 0.001) in the 24-48 hours following drug administration, as compared to the retrospective controls (N=41). The probabilities of fever resolution or CRP decline did not appear to be dose-related in this small study (p=0.80 and p=0.10, respectively). Within the 28-day follow-up, 5 (15.6%) patients died. For patients who recovered, median time to clinical recovery was 3 days (IQR, 2-5). Clinically presumed and/or cultured bacterial superinfections were reported in 5 (15.6%) patients. Correlative biological studies demonstrated that tocilizumab-treated patients produced anti-SARS-CoV-2 antibodies comparable to controls. Interpretation Low-dose tocilizumab was associated with rapid improvement in clinical and laboratory measures of hyperinflammation in hospitalized patients with Covid-19. Results of this trial and its correlative biological studies provide rationale for a randomized, controlled trial of low-dose tocilizumab in Covid-19.
Keyphrases
- low dose
- coronavirus disease
- sars cov
- rheumatoid arthritis
- end stage renal disease
- ejection fraction
- chronic kidney disease
- newly diagnosed
- juvenile idiopathic arthritis
- risk factors
- rheumatoid arthritis patients
- peritoneal dialysis
- clinical trial
- mechanical ventilation
- prognostic factors
- type diabetes
- intensive care unit
- randomized controlled trial
- insulin resistance
- pulmonary hypertension
- cross sectional
- patient reported outcomes
- systemic lupus erythematosus
- disease activity
- skeletal muscle
- adipose tissue
- acute respiratory distress syndrome
- phase iii
- binding protein
- open label
- phase ii