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. 2020 Jul 29;35:81–87. doi: 10.1016/j.prrv.2020.07.003

Table 2.

Treatment of COVID-19 with IL-6 inhibitors.

Source Xu, X et al., 2020 Luo et al., 2020 Gritti et al., 2020 Toniati et al., 2020 Klopfenstein et al., 2020 Roumier et al., 2020
Country of origin Anhui, China Wuhan, China Bergamo, Italy Brescia, Italy Nord Franche-Comté, France Suresnes, France



Center Single center Single center Single center Single center Single center Single center



Study period February 5–14, 2020 January 27–March 5, 2020 March 11–24, 2020 March 9–20, 2020 April 1–13, 2020 March 21–April 2, 2020



Type of study Retrospective cohort Retrospective cohort Retrospective cohort Prospective series Retrospective case-control Retrospective case-control



Number of patients 21 15 21 100 20 TCZ
25 Standard therapy (ST)
30 TCZ
29 Standard therapy



Age in years ¥ 56.8 ± 16.5 73 (62–80) 64 (48–75) 62 76.8 ± 11 in TCZ group
70.7 ± 15 in ST group
50



Male gender (%) 86 80 86 88 80



Follow up (days) 7 8 10 8 (6.0–9.75)



Inclusion criteria and ICU status, if reported Severe: tachypnea and/or respiratory failure
17 (81%)
Critical: mechanical ventilation or organ support on ICU
4 (19%)
Moderately, severely or critically ill (not otherwise specified) All required either CPAP or NIV NIV 57 (57%) or mechanical ventilation 43 (43%)
43 in ICU
57 in general ward (because no ICU beds available)
Failure of standard treatment, time to symptoms onset >7 days, O2 therapy ≥5 L/min, >25% lung damage on CT, ≥2 elevated markers of inflammation
TCZ group: more lung involvement on CT, lymphopenia, high CRP, higher level O2 therapy
None in ICU at enrollment (ICU admission was one of the outcomes)
Severe (O2 requirement >6 L/min, rapidly deteriorating, high CRP, with ≥5 days of prior
disease duration.
7 (23%) in ICU



IL-6 agent and dose TCZ 4–8 mg/kg body weight, recommended
dose 400 mg maximum 800 mg.
14.3% received 2nd dose 12 hours later
TCZ 80–600 mg
33% administered subsequent doses
Siltuximab median dose 900 mg × 1 for all 21;
5 patients received a second dose
TCZ 8 mg/kg (max 800 mg) by two consecutive intravenous
infusions 12 hours apart
Eighty-seven patients (87%) received 2 infusions of TCZ, 13 patients
(13%) 3 infusions
TCZ 1 or 2 doses (dose not reported) TCZ 8 mg/kg



Other treatments Lopinavir/Ritonavir
Interferon-α
Methylprednisolone
8 (53%) also received methylprednisolone Usual care (not specified) Lopinavir/ritonavir or remdesivir
antibiotics ppx, hydroxychloroquine 400 mg and dexamethasone 20 mg/day
hydroxychloroquine or lopinavir-ritonavir therapy and antibiotics, and less commonly corticosteroids 2 patients in TCZ group also received 10 day course HCQ and azithro; 2 patients in control group received high dose methylprednisolone pulses



Outcome All 21 discharged from hospital 10 (67%) stabilized
2 (13%) worsening disease
3 (20%) died
Median CRP fell from 126.9 to 11.2 m g/L
Drop in IL-6 in 67%
7 (33%) improved
9 (43%) stabilized
5 (24%) worsened and required intubation
General wards patients:
37 (65%) improved 7 (12%) stabilized
13 (23%) patients worsened
ICU patients:
32 (74%) improved 1 (2%) stabilized 10 (24%) died
Overall at 10 days: 77 (77%) improved/stable 23 (23%) worsened
20 (20%) died
Note: 3 patients had GI perforation requiring urgent surgery
TCZ group:
3 (15%) remained hospitalized
11 (55%) discharged
5 (25%) death and/or ICU
ST group:
2 (8%) remained hospitalized
8 (32%) required invasive mechanical ventilation;
11 (44%) discharged
18 (72%) death and/or ICU admission
12 (48%) death
TCZ group:
4/7 (57%) discharged from ICU
6/30 (20%)
discharged from hospital
3 (10%) death
TCZ significantly reduced requirement of subsequent mechanical ventilation (weighted OR: 0.42; 95%CI [0,20–0,89] p = 0,025)
TCZ significantly reduced ICU admission (weighted OR: 0.17; 95%CI [0,06–0,48] p = 0,001)

¥ Values expressed as mean or median according to original report.

– Data not reported.

TCZ Tocilizumab.