Evidence map›Paper›PMID 34248972›Full record

ReviewFrontiers in immunology2021

Targeting Bruton's Tyrosine Kinase in CLL.

Inhye E Ahn, Jennifer R Brown

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
8.0field-weighted citation impact, top 2% 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

47 citing papers in PubMed, 76 citations in OpenAlex.

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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 1 country.

Inhye E AhnLymphoid Malignancies Section, National Heart, Lung, and Blood Institute, Bethesda, MD, United States.
Jennifer R BrownChronic Lymphocytic Leukemia Center, Division of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA, United States.
Dana-Farber Cancer Institute · USNational Heart Lung and Blood Institute · US

Funding

Unlocking the Potential of PI3K Inhibition in CLLR01CA213442 · NCI · DANA-FARBER CANCER INST · PI BROWN, JENNIFER R · 2017 to 2021
$2.9M
NCI NIH HHS R01 CA213442
6 · The paper itself

Abstract

Targeting the B-cell receptor signaling pathway through BTK inhibition proved to be effective for the treatment of chronic lymphocytic leukemia (CLL) and other B-cell lymphomas. Covalent BTK inhibitors (BTKis) led to an unprecedented improvement in outcome in CLL, in particular for high-risk subgroups with

Indexed as

AdenineAgammaglobulinaemia Tyrosine KinaseAnimalsAntineoplastic AgentsBenzamidesHumansLeukemia, Lymphocytic, Chronic, B-CellMolecular Targeted TherapyMutationPiperidinesProtein Kinase InhibitorsPyrazinesPyrazolesPyrimidinesSignal TransductionTreatment OutcomeacalabrutinibAdenineAgammaglobulinaemia Tyrosine KinaseAntineoplastic AgentsBenzamidesBTK protein, humanibrutinibPiperidinesProtein Kinase InhibitorsPyrazinesPyrazolesPyrimidineszanubrutinibacalabrutinibB-cell receptor signaling pathwayBruton’s tyrosine kinasechronic lymphocytic leukemiaibrutinibzanubrutinib

Identifiers

PMID34248972
PMCPMC8261291
OpenAlexW3175740856

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.