Evidence map›Paper›PMID 35222433›Full record

ArticleFrontiers in immunology2022

Case Report: Rapid Desensitization to Ocrelizumab for Multiple Sclerosis Is Effective and Safe.

Marcelo Vivolo Aun, Fernando Freua, Victor Hugo Rocha Marussi, Pedro Giavina-Bianchi

Open access · goldAbstract readCase Reports
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. Article
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

4 authors at 2 institutions in 1 country.

Marcelo Vivolo AunFaculdade Israelita de Ciências da Saúde Albert Einstein School of Medicine, São Paulo, Brazil.
Fernando FreuaDepartment of Neurology, Hospital Beneficência Portuguesa de São Paulo, São Paulo, Brazil.
Victor Hugo Rocha MarussiDepartment of Neurology, Hospital Beneficência Portuguesa de São Paulo, São Paulo, Brazil.
Pedro Giavina-BianchiClinical Immunology and Allergy Division, University of Sao Paulo School of Medicine, São Paulo, Brazil.
Universidade de São Paulo · BRBeneficência Portuguesa de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monoclonal antibodies have become a mainstay of treatment for many inflammatory diseases and malignancies. Multiple sclerosis is a chronic inflammatory, demyelinating, and neurodegenerative disease of the central nervous system and a common cause of disability in young adults. Ocrelizumab is a recombinant humanized monoclonal antibody that targets CD20-positive B cells and has been approved in the treatment of multiple sclerosis. Although considered safe, more than 30% of patients treated with Ocrelizumab developed infusion-related reactions, mostly regarded as mild. When severe, they can lead to a definite suspension of that drug. We present a case report of Ocrelizumab desensitization in a female patient who presented an immediate hypersensitivity reaction (urticaria and angioedema) during the first Ocrelizumab infusion. Although mechanisms involved in the response were not elucidated, the procedure occurred uneventfully and permitted first-line multiple sclerosis treatment maintenances. Desensitization should be considered a safe therapeutic option in patients with immediate hypersensitivity reactions to Ocrelizumab.

Indexed as

Hypersensitivity, ImmediateMultiple SclerosisNeurodegenerative DiseasesAntibodies, Monoclonal, HumanizedFemaleHumansYoung AdultAntibodies, Monoclonal, Humanizedocrelizumaballergydesensitizationhypersensitivitymonoclonal antibodiesmultiple sclerosisOcrelizumab

Identifiers

PMID35222433
PMCPMC8865367
OpenAlexW4211197996

What OpenQuestion holds

Textmetadata
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.