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Compassionate Use of Tocilizumab for Treatment of SARS-CoV-2 Pneumonia.
Jordan, Stanley C; Zakowski, Phillip; Tran, Hai P; Smith, Ethan A; Gaultier, Cyril; Marks, Gregory; Zabner, Rachel; Lowenstein, Hayden; Oft, Jillian; Bluen, Benjamin; Le, Catherine; Shane, Rita; Ammerman, Noriko; Vo, Ashley; Chen, Peter; Kumar, Sanjeev; Toyoda, Mieko; Ge, Shili; Huang, Edmund.
  • Jordan SC; Department of Medicine, Division of Nephrology, Transplant Immunology Laboratory, Transplant Immunotherapy Program, Los Angeles, California, USA.
  • Zakowski P; Division of Infectious Diseases, Los Angeles, California, USA.
  • Tran HP; Department of Pharmacy Services, Los Angeles, California, USA.
  • Smith EA; Department of Pharmacy Services, Los Angeles, California, USA.
  • Gaultier C; Division of Infectious Diseases, Los Angeles, California, USA.
  • Marks G; Department of Pharmacy Services, Los Angeles, California, USA.
  • Zabner R; Division of Infectious Diseases, Los Angeles, California, USA.
  • Lowenstein H; Division of Infectious Diseases, Los Angeles, California, USA.
  • Oft J; Division of Infectious Diseases, Los Angeles, California, USA.
  • Bluen B; Division of Infectious Diseases, Los Angeles, California, USA.
  • Le C; Division of Infectious Diseases, Los Angeles, California, USA.
  • Shane R; Department of Pharmacy Services, Los Angeles, California, USA.
  • Ammerman N; Department of Medicine, Division of Nephrology, Transplant Immunology Laboratory, Transplant Immunotherapy Program, Los Angeles, California, USA.
  • Vo A; Department of Medicine, Division of Nephrology, Transplant Immunology Laboratory, Transplant Immunotherapy Program, Los Angeles, California, USA.
  • Chen P; Division of Pulmonary and Critical Care Medicine, Cedars-Sinai Medical Center, Los Angeles, California, USA.
  • Kumar S; Department of Medicine, Division of Nephrology, Transplant Immunology Laboratory, Transplant Immunotherapy Program, Los Angeles, California, USA.
  • Toyoda M; Department of Medicine, Division of Nephrology, Transplant Immunology Laboratory, Transplant Immunotherapy Program, Los Angeles, California, USA.
  • Ge S; Department of Medicine, Division of Nephrology, Transplant Immunology Laboratory, Transplant Immunotherapy Program, Los Angeles, California, USA.
  • Huang E; Department of Medicine, Division of Nephrology, Transplant Immunology Laboratory, Transplant Immunotherapy Program, Los Angeles, California, USA.
Clin Infect Dis ; 71(12): 3168-3173, 2020 12 15.
Article in English | MEDLINE | ID: covidwho-612034
ABSTRACT

BACKGROUND:

Preliminary data from severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pneumonia patients indicate that a cytokine storm may increase morbidity and mortality. Tocilizumab (anti-IL-6R) is approved by the Food and Drug Administration for treatment of cytokine storm associated with chimeric antigen receptor T-cell therapy. Here we examined compassionate use of tocilizumab in patients with SARS-CoV-2 pneumonia.

METHODS:

We report on a single-center study of tocilizumab in hospitalized patients with SARS-CoV-2 pneumonia. All patients had confirmed SARS-CoV-2 pneumonia and oxygen saturations <90% on oxygen support with most intubated. We examined clinical and laboratory parameters including oxygen and vasopressor requirements, cytokine profiles, and C-reactive protein (CRP) levels pre- and post-tocilizumab treatment.

RESULTS:

Twenty-seven SARS-CoV-2 pneumonia patients received one 400 mg dose of tocilizumab. Interleukin (IL)-6 was the predominant cytokine detected at tocilizumab treatment. Significant reductions in temperature and CRP were seen post-tocilizumab. However, 4 patients did not show rapid CRP declines, of whom 3 had poorer outcomes. Oxygen and vasopressor requirements diminished over the first week post-tocilizumab. Twenty-two patients required mechanical ventilation; at last follow-up, 16 were extubated. Adverse events and serious adverse events were minimal, but 2 deaths (7.4%) occurred that were felt unrelated to tocilizumab.

CONCLUSIONS:

Compared to published reports on the morbidity and mortality associated with SARS-CoV-2, tocilizumab appears to offer benefits in reducing inflammation, oxygen requirements, vasopressor support, and mortality. The rationale for tocilizumab treatment is supported by detection of IL-6 in pathogenic levels in all patients. Additional doses of tocilizumab may be needed for those showing slow declines in CRP. Proof of efficacy awaits randomized, placebo-controlled clinical trials.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Cohort study / Experimental Studies / Prognostic study / Randomized controlled trials Topics: Vaccines Limits: Adult / Aged / Humans / Male / Middle aged Language: English Journal: Clin Infect Dis Journal subject: Communicable Diseases Year: 2020 Document Type: Article Affiliation country: Cid

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Cohort study / Experimental Studies / Prognostic study / Randomized controlled trials Topics: Vaccines Limits: Adult / Aged / Humans / Male / Middle aged Language: English Journal: Clin Infect Dis Journal subject: Communicable Diseases Year: 2020 Document Type: Article Affiliation country: Cid