Evidence map›Paper›PMID 27776353›Full record

ReviewOncotarget2017

Bruton tyrosine kinase inhibitor ONO/GS-4059: from bench to bedside.

Jingjing Wu, Mingzhi Zhang, Delong Liu

Open access · diamondAbstract readReview
In one paragraph

Review in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

16 citing papers in PubMed, 28 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

3 authors at 1 institution in 1 country.

Jingjing WuDepartment of Oncology, The first Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Mingzhi ZhangDepartment of Oncology, The first Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Delong LiuDepartment of Oncology, The first Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
First Affiliated Hospital of Zhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Bruton tyrosine kinase (BTK) inhibitor, ibrutinib, has been approved for the treatment of chronic lymphocytic leukemia, mantle cell lymphoma, and Waldenstrom's macroglobulinemia. Acquired resistance to ibrutinib due to BTK C481S mutation has been reported. Mutations in PLCγ2 can also mediate resistance to ibrutinib. Untoward effects due to off-target effects are also disadvantages of ibrutinib. More selective and potent BTK inhibitors (ACP-196, ONO/GS-4059, BGB-3111, CC-292) are being investigated. This review summarized the preclinical research and clinical data of ONO/GS-4059.

Indexed as

Agammaglobulinaemia Tyrosine KinaseClinical Trials as TopicDrug Resistance, NeoplasmHumansImidazolesLeukemia, Lymphocytic, Chronic, B-CellLymphoma, Mantle-CellMutationPhospholipase C gammaProtein-Tyrosine KinasesPyrimidinesTreatment OutcomeWaldenstrom MacroglobulinemiaAgammaglobulinaemia Tyrosine KinaseBTK protein, humanImidazolesPhospholipase C gammaProtein-Tyrosine KinasesPyrimidinestirabrutinibBruton tyrosine kinaseibrutinibONO/GS-4059

Identifiers

PMID27776353
PMCPMC5351700
OpenAlexW2535927310

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.