Evidence map›Paper›PMID 34776981›Full record

ArticleFrontiers in pharmacology2021

Safety Profile of Ibrutinib: An Analysis of the WHO Pharmacovigilance Database.

Marion Allouchery, Cécile Tomowiak, Thomas Lombard, Marie-Christine Pérault-Pochat, Francesco Salvo

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Pathogenetic Mechanism of Macular Edema During Treatment with Ibrutinib.Mediterranean journal of hematology and infectious diseases · 2026
    Article
  3. Article
  4. Article
  5. Beyond Atrial Fibrillation and Heart Failure: Ibrutinib-induced Pericardial Effusion.Journal of community hospital internal medicine perspectives · 2025
    Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Cardiotoxicity Induced by Protein Kinase Inhibitors in Patients with Cancer.International journal of molecular sciences · 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

5 authors at 3 institutions in 1 country.

Marion AlloucheryPharmacologie Clinique et Vigilances, CHU de Poitiers, Poitiers, France.
Cécile TomowiakOnco-Hématologie et Thérapie Cellulaire, CHU de Poitiers, Poitiers, France.
Thomas LombardPharmacie à Usage Intérieur, CHU de Poitiers, Poitiers, France.
Marie-Christine Pérault-PochatPharmacologie Clinique et Vigilances, CHU de Poitiers, Poitiers, France.
Francesco SalvoUniversité de Bordeaux, INSERM, BPH, UMR1219, Bordeaux, France.
Inserm · FRUniversité de Bordeaux · FRGestion de l'Eau, Acteurs, Usages · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As ibrutinib has become a standard of care in B-cell malignancies in monotherapy or in combination with other agents, definition of its safety profile appears essential. The aim of this study was to further characterize the safety profile of ibrutinib through the identification of potential safety signals in a large-scale pharmacovigilance database. All serious individual case safety reports (ICSRs) in patients aged ≥18 years involving ibrutinib suspected in the occurrence of serious adverse drug reactions or drug interacting from November 13th, 2013 to December 31st, 2020 were extracted from VigiBase, the World Health Organization global safety database. Disproportionality reporting was assessed using the information component (IC) and the proportional reporting ratio (PRR), with all other anticancer drugs used as the reference group. To mitigate the confounding of age, two subgroups were considered: patients aged<75 years and ≥75 years. A signal of disproportionate reporting (SDR) was defined if both IC and PRR were significant. A total of 16,196 ICSRs were included. The median age of patients was 72.9 years, 42.6% of ICSRs concerned patients aged ≥75 years, and 64.2% male patients. More than half (56.2%) of ICSRs resulted in hospitalization or prolonged hospitalization. Among 713 SDRs, 36 potential safety signals emerged in ibrutinib-treated patients, mainly ischemic heart diseases, pericarditis, uveitis, retinal disorders and fractures. All potential safety signals having arisen in this analysis may support patient care and monitoring of ongoing clinical trials. However, owing to the mandatory limitations of this study, our results need further confirmation using population-based studies.

Indexed as

adverse drug reactionBruton’s tyrosine kinase inhibitordrug safetyibrutinibpharmacovigilance

Identifiers

PMID34776981
PMCPMC8580940
OpenAlexW3208191940

What OpenQuestion holds

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LicenceCC BY
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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.