Real-life use of tocilizumab with or without corticosteroid in hospitalized patients with moderate-to-severe COVID-19 pneumonia: A retrospective cohort study

被引:7
|
作者
Russo, Gianluca [1 ]
Solimini, Angelo [1 ]
Zuccala, Paola [2 ]
Zingaropoli, Maria Antonella [1 ]
Carraro, Anna [2 ]
Pasculli, Patrizia [1 ]
Perri, Valentina [1 ]
Marocco, Raffaella [2 ]
Kertusha, Blerta [2 ]
Del Borgo, Cosmo [2 ]
Del Giudice, Emanuela [2 ]
Fondaco, Laura [2 ]
Tieghi, Tiziana [2 ]
D'Agostino, Claudia [1 ]
Oliva, Alessandra [1 ]
Vullo, Vincenzo [1 ]
Ciardi, Maria Rosa [1 ]
Mastroianni, Claudio Maria [1 ]
Lichtner, Miriam [1 ,2 ]
机构
[1] Sapienza Univ Rome, Policlin Umberto Hosp 1, Dept Publ Hlth & Infect Dis, Rome, Italy
[2] Sapienza Univ Rome, S Maria Goretti Hosp, Infect Dis Unit, Latina, Italy
来源
PLOS ONE | 2021年 / 16卷 / 09期
关键词
OFF-LABEL USE; MULTICENTER; MORTALITY;
D O I
10.1371/journal.pone.0257376
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Objective To evaluate the effectiveness of Tocilizumab (with or without corticosteroids) in a real-life context among moderate-to-severe COVID-19 patients hospitalized at the Infectious Diseases ward of two hospitals in Lazio region, Italy, during the first wave of SARS-CoV-2 pandemic. Method We conducted a retrospective cohort study among moderate-to-severe COVID-19 pneumonia to assess the influence of tocilizumab (with or without corticosteroids) on: 1) primary composite outcome: risk for death/invasive mechanical ventilation/ICU-transfer at 14 days from hospital admission; 2) secondary outcome: COVID-related death only. Both outcomes were also assessed at 28 days and restricted to baseline more severe cases. We also evaluated the safety of tocilizumab. Results Overall, 412 patients were recruited, being affected by mild (6.8%), moderate (66.3%) or severe (26.9%) COVID-19 at baseline. The median participant' age was 63 years, 56.5% were men, the sum of comorbidities was 1.34 (+/- 1.44), and the median time from symptom onset to hospital admission was 7 [3-10] days. Patients were subdivided in 4 treatment groups: standard of care (SoC) only (n = 172), SoC plus corticosteroid (n = 65), SoC plus tocilizumab (n = 50), SoC plus tocilizumab and corticosteroid (n = 125). Twenty-six (6.3%) patients underwent intubation, and 37 (9%) COVID-related deaths were recorded. After adjusting for several factors, multivariate analysis showed that tocilizumab (with or without corticosteroids) was associated to improved primary and secondary outcomes at 14 days, and at 28-days only when tocilizumab administered without corticosteroid. Among more severe cases the protective effect of tocilizumab (+/- corticosteroids) was observed at both time-points. No safety concerns were recorded. Conclusion Although contrasting results from randomized clinical trials to date, in our experience tocilizumab was a safe and efficacious therapeutic option for patients with moderate-to-severe COVID-19 pneumonia. Its efficacy was improved by the concomitant administration of corticosteroids in patients affected by severe-COVID-19 pneumonia at baseline.
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页数:20
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