Evidence map›Paper›PMID 31582362›Full record

Trial reportBlood2019

Hypertension and incident cardiovascular events following ibrutinib initiation.

Tyler Dickerson, Tracy Wiczer, Allyson Waller, Jennifer Philippon, Kyle Porter, Devin Haddad, Avirup Guha, Kerry A Rogers, Seema Bhat, John C Byrd and 3 more

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Blood, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 146 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
146citing papers in PubMed, 1 pooled it
15.7field-weighted citation impact, top 1% 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

146 citing papers in PubMed, 1 synthesis or guideline pooled it, 241 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Acalabrutinib Versus Ibrutinib in Previously Treated Chronic Lymphocytic Leukemia: Results of the First Randomized Phase III Trial.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2021
    Trial
  7. Trial
  8. Stratifying Cardiovascular Risk in Patients With HCC Receiving Atezolizumab/Bevacizumab: A Comparison of ESC and CARDIOSOR Scores.Liver international : official journal of the International Association for the Study of the Liver · 2026
    Observational
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Cardiovascular Toxicity of BTKi in Chronic B-Cell Malignancies.Reviews in cardiovascular medicine · 2026
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

86 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 1 country.

Tyler DickersonDepartment of Pharmacy, James Cancer Hospital and Solove Research Institute, and.
Tracy WiczerDepartment of Pharmacy, James Cancer Hospital and Solove Research Institute, and.
Allyson WallerDepartment of Pharmacy, James Cancer Hospital and Solove Research Institute, and.
Jennifer PhilipponDepartment of Pharmacy, James Cancer Hospital and Solove Research Institute, and.
Kyle PorterCenter for Biostatistics, Department of Biomedical Informatics, The Ohio State University, Columbus, OH.
Devin HaddadCardio-oncology Program, Division of Cardiology, The Ohio State University Medical Center, Columbus, OH; and.
Avirup GuhaCardio-oncology Program, Division of Cardiology, The Ohio State University Medical Center, Columbus, OH; and.
Kerry A RogersDivision of Hematology, The Ohio State University, Columbus, OH.
Seema BhatDivision of Hematology, The Ohio State University, Columbus, OH.
John C ByrdDivision of Hematology, The Ohio State University, Columbus, OH.
Jennifer A WoyachDivision of Hematology, The Ohio State University, Columbus, OH.
Farrukh AwanDivision of Hematology, The Ohio State University, Columbus, OH.
Daniel AddisonCardio-oncology Program, Division of Cardiology, The Ohio State University Medical Center, Columbus, OH; and.
The Ohio State University · USThe Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute · USThe Ohio State University Wexner Medical Center · US

Funding

Translational Training Grant in Experimental TherapeuticsK12CA133250 · NCI · OHIO STATE UNIVERSITY · PI WILLIAM E. CARSON, Rosa Lapalombella · 2008 to 2026
$15.0M
Targeted Therapy for LeukemiaR35CA197734 · NCI · UNIVERSITY OF CINCINNATI · PI BYRD, JOHN C. · 2015 to 2021
$6.6M
Improving BTK Directed Therapy for CLLR01CA197870 · NCI · OHIO STATE UNIVERSITY · PI WOYACH, JENNIFER A. · 2015 to 2019
$1.8M
Targeted Therapies and Mechanisms of Resistance in Chronic Lymphocytic LeukemiaK23CA178183 · NCI · OHIO STATE UNIVERSITY · PI WOYACH, JENNIFER A. · 2013 to 2017
$866k
NCI NIH HHS K12 CA133250NCI NIH HHS K23 CA178183NCI NIH HHS R01 CA197870NCI NIH HHS R35 CA197734
6 · The paper itself

Abstract

Ibrutinib is associated with dramatic efficacy against B-cell malignancies. Yet, it has been linked with potentially limiting cardiotoxicity, including emerging reports of profound hypertension (HTN). The long-term incidence, severity, and impact of HTN development with ibrutinib are unknown. Therefore, in 562 consecutive patients treated with ibrutinib for B-cell malignancies from 2009 through 2016, we assessed the new/incident or worsened HTN (systolic blood pressure [BP] cutoff, 130 mm Hg). Observed incident HTN rates were compared with Framingham-heart-predicted incident HTN rates. We also evaluated the relationship of HTN to the development of other major adverse cardiovascular events (MACEs), including arrhythmia, myocardial infarction, stroke, heart failure, and cardiovascular death. Further, we assessed the effects of different antihypertensive classes on ibrutinib-related HTN. Overall, 78.3% of ibrutinib users developed new or worsened HTN over a median of 30 months. New HTN developed in 71.6% of ibrutinib users, with a time to 50% cumulative incidence of 4.2 months. Among those without preceding HTN, 17.7% developed high-grade HTN (BP >160/100 mm Hg). In multivariate regression, new or worsened HTN was associated with increased MACEs (hazard ratio [HR], 2.17; 95% confidence interval [CI], 1.08-4.38). No single antihypertensive class was associated with prevention or control of ibrutinib-related HTN. However, antihypertensive initiation was associated with a lower risk of a MACE (HR, 0.40; 95% CI, 0.24-0.66). Collectively, these data suggest that ibrutinib is associated with a substantial increase in the incidence and severity of HTN, and that HTN development carries a higher risk of subsequent cardiotoxic events.

Indexed as

Hematologic NeoplasmsHypertensionPyrazolesPyrimidinesStrokeAdenineAgedAntihypertensive AgentsFemaleHeart DiseasesHumansIncidenceMaleMiddle AgedPiperidinesAdenineAntihypertensive AgentsibrutinibPiperidinesPyrazolesPyrimidines

Identifiers

PMID31582362
PMCPMC6887116
OpenAlexW2978550355

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.