Evidence map›Paper›PMID 35960720›Full record

Trial reportPloS one2022

Timely administration of tocilizumab improves outcome of hospitalized COVID-19 patients.

Abraham Rutgers, Peter E Westerweel, Bronno van der Holt, Simone Postma, Marit G A van Vonderen, Djura P Piersma, Douwe Postma, Maarten van den Berge, Eefje Jong, Marten de Vries and 19 more

Open access · goldAbstract readClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 4 pooled it
1.8field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 4 syntheses or guidelines pooled it, 22 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

29 authors at 12 institutions in 1 country.

Abraham RutgersDepartment of Rheumatology and Clinical Immunology, University Medical Center Groningen, Groningen, The Netherlands.
Peter E WesterweelDepartment of Internal Medicine, Albert Schweitzer Hospital, Dordrecht, The Netherlands.ORCID 0000-0002-0746-7039
Bronno van der HoltHOVON Data Center, Department of Haematology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.ORCID 0000-0001-6414-2671
Simone PostmaDepartment of Haematology, University Medical Center Groningen, Groningen, The Netherlands.
Marit G A van VonderenDepartment of Internal Medicine, Medical Center Leeuwarden, Leeuwarden, The Netherlands.
Djura P PiersmaDepartment of Internal Medicine, Medisch Spectrum Twente, Enschede, The Netherlands.
Douwe PostmaDepartment of Internal Medicine, University Medical Center Groningen, Groningen, The Netherlands.ORCID 0000-0002-0675-8459
Maarten van den BergeDepartment of Pulmonology, University Medical Center Groningen, Groningen, The Netherlands.
Eefje JongDepartment of Infectious Diseases, Meander MC, Amersfoort, The Netherlands.
Marten de VriesDepartment of Pulmonology, Tjongerschans Hospital, Heerenveen, The Netherlands.
Leonie van der BurgDepartment of Internal Medicine, Antonius Hospital Sneek, Sneek, The Netherlands.
Dennis HuugenDepartment of Internal Medicine, Deventer Hospital, Deventer, The Netherlands.
Marjolein van der PoelDepartment of Internal Medicine, Maastricht University Medical Centre+, Maastricht, The Netherlands.
Linda M KampschreurDepartment of Internal Medicine, Medical Center Leeuwarden, Leeuwarden, The Netherlands.
Marcel NijlandDepartment of Haematology, University Medical Center Groningen, Groningen, The Netherlands.
Jaap H StrijbosDepartment of Pulmonology, Nij Smellinghe Hospital, Drachten, The Netherlands.
Menno TammingaDepartment of Pulmonology, University Medical Center Groningen, Groningen, The Netherlands.ORCID 0000-0001-6508-2623
Pim G N J MutsaersDepartment of Haematology, Erasmus Medical Center, Rotterdam, The Netherlands.
Suzanne Schol-GelokDepartment of Internal Medicine, Albert Schweitzer Hospital, Dordrecht, The Netherlands.
Margriet Dijkstra-TiekstraDepartment of Haematology, University Medical Center Groningen, Groningen, The Netherlands.
Grigory SidorenkovDepartment of Epidemiology, University Medical Center Groningen, Groningen, The Netherlands.
Julien VincentenDepartment of Pulmonology, Albert Schweitzer Hospital, Dordrecht, The Netherlands.
Wouter H van GeffenDepartment of Pulmonology, Medical Center Leeuwarden, Leeuwarden, The Netherlands.
Marjolein KnoesterDepartment of Medical Microbiology, University Medical Center Groningen, Groningen, The Netherlands.
Jos KosterinkPharmacy, University Medical Center Groningen, Groningen, The Netherlands.
Reinold GansDepartment of Internal Medicine, University Medical Center Groningen, Groningen, The Netherlands.
Coen StegemanDepartment of Internal Medicine, University Medical Center Groningen, Groningen, The Netherlands.
Gerwin HulsDepartment of Haematology, University Medical Center Groningen, Groningen, The Netherlands.
Tom van MeertenDepartment of Haematology, University Medical Center Groningen, Groningen, The Netherlands.
University Medical Center Groningen · NLAlbert Schweitzer Ziekenhuis · NLMedisch Centrum Leeuwarden · NLDeventer Ziekenhuis · NLErasmus MC · NLErasmus MC Cancer Institute · NLMaastricht University Medical Centre · NLMeander Medisch Centrum · NLMedisch Spectrum Twente · NL's Heeren Loo · NLSt. Antonius Ziekenhuis · NLZiekenhuis Nij Smellinghe · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe aim of this study was to determine the efficacy of early tocilizumab treatment for hospitalized patients with COVID-19 disease.

methodsOpen-label randomized phase II clinical trial investigating tocilizumab in patients with proven COVID-19 admitted to the general ward and in need of supplemental oxygen. The primary endpoint of the study was 30-day mortality with a prespecified 2-sided significance level of α = 0.10. A post-hoc analysis was performed for a combined endpoint of mechanical ventilation or death at 30 days. Secondary objectives included comparing the duration of hospital stay, ICU admittance and duration of ICU stay and the duration of mechanical ventilation.

resultsA total of 354 patients (67% men; median age 66 years) were enrolled of whom 88% received dexamethasone. Thirty-day mortality was 19% (95% CI 14%-26%) in the standard arm versus 12% (95% CI: 8%-18%) in the tocilizumab arm, hazard ratio (HR) = 0.62 (90% CI 0.39-0.98; p = 0.086). 17% of patients were admitted to the ICU in each arm (p = 0.89). The median stay in the ICU was 14 days (IQR 9-28) in the standard arm versus 9 days (IQR 5-14) in the tocilizumab arm (p = 0.014). Mechanical ventilation or death at thirty days was 31% (95% CI 24%-38%) in the standard arm versus 21% (95% CI 16%-28%) in the tocilizumab arm, HR = 0.65 (95% CI 0.42-0.98; p = 0.042).

conclusionsThis randomized phase II study supports efficacy for tocilizumab when given early in the disease course in hospitalized patients who need oxygen support, especially when concomitantly treated with dexamethasone.

trial registrationhttps://www.trialregister.nl/trial/8504.

Indexed as

COVID-19 Drug TreatmentAgedAntibodies, Monoclonal, HumanizedDexamethasoneFemaleHumansMaleOxygenRespiration, ArtificialSARS-CoV-2Treatment OutcomeAntibodies, Monoclonal, HumanizedDexamethasoneOxygentocilizumab

Identifiers

PMID35960720
PMCPMC9374226
OpenAlexW4290851888

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.