Evidence map›Paper›PMID 30642919›Full record

ReviewBlood2019

How I manage ibrutinib intolerance and complications in patients with chronic lymphocytic leukemia.

Deborah M Stephens, John C Byrd

Open access · bronzeAbstract readCase ReportsReview
In one paragraph

Review in Blood, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed, 1 pooled it
14.7field-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

66 citing papers in PubMed, 1 synthesis or guideline pooled it, 143 citations in OpenAlex.

  1. Guideline
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  4. Population Pharmacokinetics of Ibrutinib in Healthy Adults.European journal of drug metabolism and pharmacokinetics · 2021
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6 more citing papers are in PubMed but not listed here.

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 at 2 institutions in 2 countries.

Deborah M StephensDivision of Hematology and Hematologic Malignancies, Department of Internal Medicine, University of Utah, Salt Lake City, UT; and.ORCID 0000-0001-9188-5008
John C ByrdDivision of Hematology, Department of Internal Medicine.
Institute of Medicinal Plant Development · CNUniversity of Utah · US

Funding

Targeted Therapy for LeukemiaR35CA197734 · NCI · UNIVERSITY OF CINCINNATI · PI BYRD, JOHN C. · 2015 to 2021
$6.6M
Novel Strategies to Eliminate Resistance to B-cell Receptor Inhibitor Therapy in Lymphoid MalignanciesK23CA212271 · NCI · UNIVERSITY OF UTAH · PI STEPHENS, DEBORAH · 2016 to 2020
$902k
NCI NIH HHS K23 CA212271NCI NIH HHS R35 CA197734
6 · The paper itself

Abstract

Chronic lymphocytic leukemia (CLL) therapy has changed dramatically with the introduction of several targeted therapeutics. Ibrutinib was the first approved for use in 2014 and now is used for initial and salvage therapy of CLL patients. With its widespread use in clinical practice, ibrutinib's common and uncommon adverse events reported less frequently in earlier clinical trials have been experienced more frequently in real-world practice. In particular, atrial fibrillation, bleeding, infections, and arthralgias have been reported. The management of ibrutinib's adverse events often cannot be generalized but must be individualized to the patient and their long-term risk of additional complications. When ibrutinib was initially developed, there were limited therapeutic alternatives for CLL, which often resulted in treating through the adverse events. At the present time, there are several effective alternative agents available, so transition to an alternative CLL directed therapy may be considered. Given the continued expansion of ibrutinib across many therapeutic areas, investigation of the pathogenesis of adverse events with this agent and also clinical trials examining therapeutic approaches for complications arising during therapy are needed. Herein, we provide strategies we use in real-world CLL clinical practice to address common adverse events associated with ibrutinib.

Indexed as

AdenineAgedAnticoagulantsAnti-Infective AgentsArthralgiaAtrial FibrillationDrug Resistance, NeoplasmFemaleHemorrhageHumansInfectionsLeukemia, Lymphocytic, Chronic, B-CellMaleMiddle AgedPiperidinesPrognosisAdenineAnticoagulantsAnti-Infective AgentsibrutinibPiperidinesPyrazolesPyrimidines

Identifiers

PMID30642919
PMCPMC6428663
OpenAlexW2909557351

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.