Evidence map›Paper›PMID 40737507›Full record

ReviewThe oncologist2025

Considerations for the practical management of cardiovascular risk with Bruton's tyrosine kinase inhibitors for patients with chronic lymphocytic leukemia.

Daniel Lenihan, Michelle Bloom, Robert Copeland-Halperin, Matthew R Fleming, Michael Fradley, Rupal O'Quinn, Seema A Bhat

Abstract readReview
In one paragraph

Review in The oncologist, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–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

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Cardiovascular Toxicity of BTKi in Chronic B-Cell Malignancies.Reviews in cardiovascular medicine · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. 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

7 authors.

Daniel LenihanCardio-Oncology Center of Excellence, Cardiac Rehabilitation, and Heart Failure Clinic, Saint Francis Healthcare System, MO 63703, United States.ORCID 0000-0001-9458-0154
Michelle BloomCardio-oncology program, NYU Langone Health, New York, NY 11501, United States.
Robert Copeland-HalperinCardiology, Northwell Health, New York, NY 11040, United States.
Matthew R FlemingCardiovascular Medicine, Vanderbilt University Medical Center, Nashville, TN 37232, United States.
Michael FradleyCardio-oncology, Hospital of the University of Pennsylvania, Philadelphia, PA 19104, United States.
Rupal O'QuinnCardiovascular Division, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 43210, United States.
Seema A BhatHematology, The Ohio State University Comprehensive Cancer Center, Columbus, OH 43210, United States.

Funding

Vanderbilt Clinical Oncology Research Career Development ProgramK12CA090625 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Debra L. Friedman, Paula Jill Hurley · 2001 to 2026
$16.9M
AstraZenecaNCI NIH HHS K12 CA090625
6 · The paper itself

Abstract

backgroundBruton's tyrosine kinase inhibitors (BTKis) are central to the medical management of chronic lymphocytic leukemia. However, accumulating data suggest an important association with cardiovascular (CV) adverse events (AEs), including arrhythmias, hypertension, and bleeding, in patients with chronic lymphocytic leukemia and other hematological malignancies treated with this therapeutic class. Data from comparative trials with BTKis suggest second-generation agents, for example, acalabrutinib and zanubrutinib, may be associated with fewer CV AEs than first-in-class BTKi ibrutinib.

methodsPubMed and the proceedings of key hematology congresses were searched for relevant information using broad search terms, including chronic lymphocytic leukemia, BTKi, and toxicity.

resultsWhen managing patients with chronic lymphocytic leukemia, screening before and during treatment to assess CV risk is suggested to guide decision-making. Due to the increased toxicity with ibrutinib, the second-generation BTKis are now preferred (per the NCCN Clinical Practice Guidelines in Oncology [NCCN Guidelines]). For patients with a high CV risk, the decision between second-generation BTKi or a time-limited alternative, like venetoclax plus an anti-CD20 monoclonal antibody, should be made on an individual basis after patient consultation and consideration of the presenting characteristics of chronic lymphocytic leukemia in any given patient. The management of anticoagulant/antiplatelet medication during BTKi treatment requires specific attention, with coexistent medications being carefully assessed before starting a BTKi to reduce the risk of bleeding. For patients with a new-onset or worsening CV events during BTKi therapy, management may involve temporarily stopping the BTKi or switching to another class of therapy. To ensure the best outcomes, a collaborative care approach is essential, and some patients may need to be referred to a cardiologist/cardio-oncologist for specialist management.

conclusionBaseline and ongoing CV risk assessment, careful monitoring, management, and a multidisciplinary team approach are all critical to ensure optimal oncologic and CV outcomes for patients with chronic lymphocytic leukemia receiving BTKis.

Indexed as

Agammaglobulinaemia Tyrosine KinaseCardiovascular DiseasesLeukemia, Lymphocytic, Chronic, B-CellProtein Kinase InhibitorsAdenineBenzamidesHumansPiperidinesPyrazinesPyrazolesPyrimidinesTyrosine Kinase InhibitorsacalabrutinibAdenineAgammaglobulinaemia Tyrosine KinaseBenzamidesBTK protein, humanibrutinibPiperidinesProtein Kinase InhibitorsPyrazinesPyrazolesPyrimidinesTyrosine Kinase InhibitorsarrhythmiaBruton’s tyrosine kinase inhibitorcardiovascularchronic lymphocytic leukemiahemorrhagehypertension

Identifiers

PMID40737507
PMCPMC12548057

What OpenQuestion holds

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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.