Evidence map›Paper›PMID 34177947›Full record

ReviewFrontiers in immunology2021

Resistance Mutations to BTK Inhibitors Originate From the NF-κB but Not From the PI3K-RAS-MAPK Arm of the B Cell Receptor Signaling Pathway.

C I Edvard Smith, Jan A Burger

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 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
6.5field-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

41 citing papers in PubMed, 63 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 2 countries.

C I Edvard SmithDepartment of Laboratory Medicine, Karolinska Institutet (KI), Huddinge, Sweden.
Jan A BurgerDepartment of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Karolinska Institutet · SEThe University of Texas MD Anderson Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since the first clinical report in 2013, inhibitors of the intracellular kinase BTK (BTKi) have profoundly altered the treatment paradigm of B cell malignancies, replacing chemotherapy with targeted agents in patients with chronic lymphocytic leukemia (CLL), mantle cell lymphoma (MCL), and Waldenström's macroglobulinemia. There are over 20 BTKi, both irreversible and reversible, in clinical development. While loss-of-function (LoF) mutations in the

Indexed as

MutationAgammaglobulinaemia Tyrosine KinaseAnimalsB-LymphocytesCARD Signaling Adaptor ProteinsDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticGuanylate CyclaseHematologic NeoplasmsHumansMitogen-Activated Protein KinasesNF-kappa BPhosphatidylinositol 3-KinasePhospholipase C gammaProtein Kinase Inhibitorsras ProteinsAgammaglobulinaemia Tyrosine KinaseBTK protein, humanCARD11 protein, humanCARD Signaling Adaptor ProteinsGuanylate CyclaseMitogen-Activated Protein KinasesNF-kappa BPhosphatidylinositol 3-KinasePhospholipase C gammaPLCG2 protein, humanProtein Kinase Inhibitorsras ProteinsB cell receptorBtkCARD11chronic lymphocytic leukemiaibrutinibmantle cell lymphomaresistance mutationWaldenström’s macroglobulinemia

Identifiers

PMID34177947
PMCPMC8222783
OpenAlexW3166816485

What OpenQuestion 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 OpenQuestion graph.