Evidence map›Paper›PMID 34894345›Full record

ReviewClinical pharmacokinetics2022

Pharmacokinetic/Pharmacodynamic Considerations of Alternate Dosing Strategies of Tocilizumab in COVID-19.

Elizabeth Leung, Ryan L Crass, Sarah C J Jorgensen, Sumit Raybardhan, Bradley J Langford, W Justin Moore, Nathaniel J Rhodes

Open access · bronzeAbstract readReview
In one paragraph

Review in Clinical pharmacokinetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 2 pooled it
1.1field-weighted citation impact, top 19% 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, 2 syntheses or guidelines pooled it, 24 citations in OpenAlex.

  1. Guideline
  2. Pooled it
  3. Trial
  4. Article
  5. Article
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  9. The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG · 2025
    Article
  10. Review
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  16. Article
  17. Drug dosing in hospitalized obese patients with COVID-19.Critical care (London, England) · 2022
    Review
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

7 authors at 6 institutions in 3 countries.

Elizabeth LeungDepartment of Pharmacy, St. Michael's Hospital/Unity Health Toronto, Toronto, ON, Canada. beth.leung@utoronto.ca.ORCID 0000-0002-7066-0886
Ryan L CrassAnn Arbor Pharmacometrics Group, Ann Arbor, MI, USA.ORCID 0000-0001-5403-4730
Sarah C J JorgensenDepartment of Pharmacy, Mount Sinai Hospital, Toronto, ON, Canada.
Sumit RaybardhanDepartment of Pharmacy, North York General, Toronto, ON, Canada.
Bradley J LangfordPublic Health Ontario, Toronto, ON, Canada.
W Justin MooreDepartment of Pharmacy, Northwestern Medicine, Chicago, IL, USA.
Nathaniel J RhodesDepartment of Pharmacy, Northwestern Medicine, Chicago, IL, USA.ORCID 0000-0002-0018-5434
Midwestern University · USMount Sinai Hospital · CANorthwestern Medicine · USNorth York General Hospital · CAPublic Health Ontario · CASt. Michael's Hospital · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tocilizumab is one of few treatments that have been shown to improve mortality in patients with coronavirus disease 2019 (COVID-19), but increased demand has led to relative global shortages. Recently, it has been suggested that lower doses, or fixed doses, of tocilizumab could be a potential solution to conserve the limited global supply while conferring equivalent therapeutic benefit to the dosing regimens studied in major trials. The relationship between tocilizumab dose, exposure, and response in COVID-19 has not been adequately characterized. There are a number of pharmacokinetic (PK) parameters that likely differ between patients with severe COVID-19 and patients in whom tocilizumab was studied during the US FDA approval process. Likewise, it is unclear whether a threshold exposure is necessary for tocilizumab efficacy. The safety and efficacy of fixed versus weight-based dosing of tocilizumab has been evaluated outside of COVID-19, but it is uncertain if these observations are generalizable to severe or critical COVID-19. In the current review, we consider the potential advantages and limitations of alternative tocilizumab dosing strategies. Leveraging PK models and simulation analyses, we demonstrate that a fixed single dose of tocilizumab 400 mg is unlikely to produce PK exposures equivalent to those achieved in the REMAP-CAP trial, although weight-stratified dosing appears to produce more uniform exposure distribution. Data from current and future trials could provide PK/pharmacodynamic insight to better inform dosing strategies at the bedside. Ultimately, rational dosing strategies that balance available limited supply with patient needs are required.

Indexed as

COVID-19 Drug TreatmentAntibodies, Monoclonal, HumanizedHumansSARS-CoV-2Antibodies, Monoclonal, Humanizedtocilizumab

Identifiers

PMID34894345
PMCPMC8665708
OpenAlexW4225824162

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.