Evidence map›Paper›PMID 32415406›Full record

ReviewCurrent hematologic malignancy reports2020

Management of Ibrutinib Toxicities: a Practical Guide.

Masa Lasica, Constantine S Tam

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current hematologic malignancy reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
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

21 citing papers in PubMed.

  1. Review
  2. Cardiovascular Safety of Bruton Tyrosine Kinase Inhibitors: From Ibrutinib to Next-Generation Agents.American journal of cardiovascular drugs : drugs, devices, and other interventions · 2026
    Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Updates of primary central nervous system lymphoma.Therapeutic advances in hematology · 2024
    Review
  9. Article
  10. Article
  11. Article
  12. Cystoid macular edema secondary to ibrutinib.American journal of ophthalmology case reports · 2022
    Article
  13. Review
  14. Upfront therapy: the case for continuous treatment.Hematology. American Society of Hematology. Education Program · 2021
    Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Review
  20. 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

2 authors.

Masa LasicaDepartment of Haematology, St Vincent's Hospital, Melbourne, Australia.
Constantine S TamDepartment of Haematology, St Vincent's Hospital, Melbourne, Australia. Constantine.Tam@petermac.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewIbrutinib is a first-in-class, highly potent Bruton tyrosine kinase inhibitor which has become standard of care for patients with chronic lymphocytic leukaemia and other lymphoproliferative disorders. It requires indefinite administration which places emphasis on toxicity and long-term tolerance. RECENT

findingsExtensive use of ibrutinib in studies and clinical practice has better defined its full toxicity profile which has made its use more challenging than initially foreseen. In particular, dysrhythmias, bleeding, infections and constitutional symptoms have been reported and can result in dose reduction or discontinuation of ibrutinib. Herein, we review the common as well as rare but important toxicities and discuss approach and management on a practical level. We also highlight that patients should be regularly monitored for adverse events and proactively treated to minimise side effects and avoid disruption.

Indexed as

AdenineAgammaglobulinaemia Tyrosine KinaseAntineoplastic AgentsDrug-Related Side Effects and Adverse ReactionsHumansPiperidinesProtein Kinase InhibitorsRisk AssessmentRisk FactorsTreatment OutcomeAdenineAgammaglobulinaemia Tyrosine KinaseAntineoplastic AgentsBTK protein, humanibrutinibPiperidinesProtein Kinase InhibitorsBleedingCLLIbrutinibIbrutinib-related AFToxicities

Identifiers

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.