Evidence map›Paper›PMID 34019122›Full record

SynthesisIntensive care medicine2021

Tocilizumab in COVID-19: a meta-analysis, trial sequential analysis, and meta-regression of randomized-controlled trials.

Timothy Arthur Chandos Snow, Naveed Saleem, Gareth Ambler, Eleni Nastouli, Mervyn Singer, Nishkantha Arulkumaran

Open access · bronzeAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Intensive care medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 3 pooled it
4.4field-weighted citation impact, top 4% 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

45 citing papers in PubMed, 3 syntheses or guidelines pooled it, 72 citations in OpenAlex.

  1. Pooled it
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  6. Real-World Tocilizumab Use in Pediatric Inpatients.The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG · 2025
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  9. Cytokine, Anti-SARS-CoV-2 Antibody, and Neutralizing Antibody Levels in Conventional Blood Donors Who Have Recovered from COVID-19.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2024
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  20. [Journal of personalized medicine · 2022
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Timothy Arthur Chandos SnowBloomsbury Institute of Intensive Care Medicine, University College London, Gower St, London, WC1E 6BT, UK. timothy.snow@doctors.net.uk.ORCID 0000-0002-8395-7857
Naveed SaleemBloomsbury Institute of Intensive Care Medicine, University College London, Gower St, London, WC1E 6BT, UK.ORCID 0000-0003-2963-6996
Gareth AmblerDepartment of Statistical Science, University College London, London, UK.ORCID 0000-0002-5322-7327
Eleni NastouliDepartment of Clinical Virology, University College London Hospital, London, UK.ORCID 0000-0002-1684-2013
Mervyn SingerBloomsbury Institute of Intensive Care Medicine, University College London, Gower St, London, WC1E 6BT, UK.ORCID 0000-0002-1042-6350
Nishkantha ArulkumaranBloomsbury Institute of Intensive Care Medicine, University College London, Gower St, London, WC1E 6BT, UK.ORCID 0000-0001-7942-8007
Bury College · GBUniversity College Hospital · GBUniversity College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeInterleukin-6 (IL-6) levels discriminate between patients with mild and severe COVID-19, making IL-6 inhibition an attractive therapeutic strategy. We conducted a systematic review, meta-analysis, trial sequential analysis (TSA), and meta-regression of randomized-controlled trials to ascertain the benefit of IL-6 blockade with tocilizumab for COVID-19.

methodsWe included randomized-controlled trials (RCTs) allocating patients with COVID-19 to tocilizumab. Our control group included standard care or placebo. Trials co-administering other pharmacological interventions for COVID-19 were not excluded. Primary outcome was 28-30 day mortality. Secondary outcomes included progression-to-severe disease defined as need for mechanical ventilation, intensive-care unit (ICU) admission, or a composite.

resultsWe identified 10 RCTs using tocilizumab, 9 of which reported primary outcome data (mortality), recruiting 6493 patients with 3358 (52.2%) allocated to tocilizumab. Tocilizumab may be associated with an improvement in mortality (24.4% vs. 29.0%; OR 0.87 [0.74-1.01]; p = 0.07; I

conclusionsFor hospitalized COVID-19 patients, there is some evidence that tocilizumab use may be associated with a short-term mortality benefit, but further high-quality data are required. Its benefits may also lie in reducing the need for mechanical ventilation.

Indexed as

COVID-19 Drug TreatmentAntibodies, Monoclonal, HumanizedHumansRandomized Controlled Trials as TopicRespiration, ArtificialSARS-CoV-2Antibodies, Monoclonal, HumanizedtocilizumabCOVID-19Immunologic factorsInterleukin-6Meta-analysis

Identifiers

PMID34019122
PMCPMC8139226
OpenAlexW3163235237

What OpenQuestion holds

Textmetadata
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.