Evidence map›Paper›PMID 24532277›Full record

ArticleNeurology2014

Daclizumab-induced adverse events in multiple organ systems in multiple sclerosis.

Jiwon Oh, Shiv Saidha, Irene Cortese, Joan Ohayon, Bibiana Bielekova, Peter A Calabresi, Scott D Newsome

Open access · bronzeAbstract read
In one paragraph

Article in Neurology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Daclizumab Therapy for Multiple Sclerosis.Cold Spring Harbor perspectives in medicine · 2019
    Review
  5. Review
  6. Article
  7. Daclizumab: Development, Clinical Trials, and Practical Aspects of Use in Multiple Sclerosis.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2017
    Review
  8. Review
  9. Daclizumab.Hospital pharmacy · 2016
    Article
  10. Article
  11. Spotlight on daclizumab: its potential in the treatment of multiple sclerosis.Degenerative neurological and neuromuscular disease · 2016
    Review
  12. Review
  13. Emerging immunopharmacological targets in multiple sclerosis.Journal of the neurological sciences · 2015
    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 1 institution in 1 country.

Jiwon OhFrom the Department of Neurology (J. Oh, S.S., P.A.C., S.D.N.), Johns Hopkins University, Baltimore; and Neuroimmunology Branch (I.C., J. Ohayon, B.B.), National Institute of Neurological Disorders and Stroke, Bethesda, MD.
Shiv Saidha
Irene Cortese
Joan Ohayon
Bibiana Bielekova
Peter A Calabresi
Scott D Newsome
National Institute of Neurological Disorders and Stroke · US

Funding

Institute for Clinical and Translational ResearchUL1TR001079 · NCATS · JOHNS HOPKINS UNIVERSITY · PI FORD, DANIEL ERNEST · 2013 to 2017
$60.1M
From therapeutic mechanisms to unraveling the pathophysiology of MSZIANS003056 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI BIELEKOVA, BIBIANA · 2009 to 2018
$14.5M
NCATS NIH HHS UL1 TR001079
6 · The paper itself

Abstract

objectiveTo report 3 patients with multiple sclerosis (MS) who presented with daclizumab-related adverse events (AEs) in multiple organ systems.

methodsA retrospective chart review was performed of patients with MS who had clinical and histopathologic findings suggestive of daclizumab-induced AEs between 2004 and 2010 at the Johns Hopkins MS Clinic. This study met criteria for exemption from review from the institutional review board.

resultsOf 20 total patients with MS who had been treated with daclizumab, 3 patients with clinical and histopathologic findings suggestive of daclizumab-induced AEs were identified. All patients were treated with Zenapax (1 mg/kg monthly IV infusions) outside of a clinical trial setting. Clinical manifestations after a mean treatment duration of 20 months consisted of diffuse rash and alopecia, diffuse lymphadenopathy, and breast nodules. Tissue histopathology demonstrated lymphocytic infiltrates with CD56-expressing cells in 2 patients (lymph node, breast nodule). On daclizumab discontinuation, the rash/alopecia and diffuse lymphadenopathy resolved, while the breast nodules stabilized.

conclusionsDaclizumab-induced AEs can occur in various organ systems after a relatively prolonged duration of exposure and require clinician awareness. Future studies are needed to better understand the relationship between natural killer cells and daclizumab-related AEs.

Indexed as

AdultAIDS-Related ComplexAntibodies, Monoclonal, HumanizedAntigens, CDBreastDaclizumabFemaleHumansImmunoglobulin GImmunosuppressive AgentsLeukemic InfiltrationLymph NodesMaleMiddle AgedMultiple SclerosisRetrospective StudiesAntibodies, Monoclonal, HumanizedAntigens, CDDaclizumabImmunoglobulin GImmunosuppressive Agents

Identifiers

PMID24532277
PMCPMC3963003
OpenAlexW1968142663

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.