Evidence map›Paper›PMID 38791284›Full record

ReviewInternational journal of molecular sciences2024

A Review of Resistance Mechanisms to Bruton's Kinase Inhibitors in Chronic Lymphocytic Leukemia.

Kamil Wiśniewski, Bartosz Puła

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

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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.

Kamil WiśniewskiDepartment of Hematology, Institute of Hematology and Transfusion Medicine, 02-776 Warsaw, Poland.ORCID 0000-0003-4164-9343
Bartosz PułaDepartment of Hematology, Institute of Hematology and Transfusion Medicine, 02-776 Warsaw, Poland.ORCID 0000-0003-0116-5002

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bruton's Tyrosine Kinase (BTK) inhibitors have become one of the most vital drugs in the therapy of chronic lymphocytic leukemia (CLL). Inactivation of BTK disrupts the B-cell antigen receptor (BCR) signaling pathway, which leads to the inhibition of the proliferation and survival of CLL cells. BTK inhibitors (BTKi) are established as leading drugs in the treatment of both treatment-naïve (TN) and relapsed or refractory (R/R) CLL. Furthermore, BTKi demonstrate outstanding efficacy in high-risk CLL, including patients with chromosome 17p deletion,

Indexed as

Agammaglobulinaemia Tyrosine KinaseDrug Resistance, NeoplasmLeukemia, Lymphocytic, Chronic, B-CellProtein Kinase InhibitorsAdenineAntineoplastic AgentsHumansMutationPhospholipase C gammaPiperidinesPyrazolesPyrimidinesAdenineAgammaglobulinaemia Tyrosine KinaseAntineoplastic AgentsBTK protein, humanibrutinibPhospholipase C gammaPiperidinesProtein Kinase InhibitorsPyrazolesPyrimidinesacalabrutinibBTK inhibitorsibrutinibpirtobrutinibresistancezanubrutinib

Identifiers

PMID38791284
PMCPMC11120758

What Socratic holds

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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.