Evidence map›Paper›PMID 28673395›Full record

ReviewHematology/oncology clinics of North America2017

Mechanisms of Resistance to FLT3 Inhibitors and the Role of the Bone Marrow Microenvironment.

Gabriel Ghiaur, Mark Levis

Open access · greenAbstract readReview
In one paragraph

Review in Hematology/oncology clinics of North America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

38 citing papers in PubMed, 70 citations in OpenAlex.

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  11. Therapeutic advances of targeting receptor tyrosine kinases in cancer.Signal transduction and targeted therapy · 2024
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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 1 institution in 1 country.

Gabriel GhiaurAdult Leukemia Program, Division of Hematological Malignancies, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, 1650 Orleans Street CRB I, Room 243, Baltimore, MD 21287, USA. Electronic address: gghiaur1@jhmi.edu.
Mark LevisAdult Leukemia Program, Division of Hematological Malignancies, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, 1650 Orleans Street CRB I, Room 2M44, Baltimore, MD 21287, USA.
Sidney Kimmel Comprehensive Cancer Center · US

Funding

Bone Marrow Microenvironmental Expression of Cytochrome P450 EnzymesK08HL127269 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI GHIAUR, GABRIEL · 2015 to 2019
$823k
NHLBI NIH HHS K08 HL127269
6 · The paper itself

Abstract

The presence of FLT3 mutations in acute myeloid leukemia (AML) carries a particularly poor prognosis, making the development of FLT3 inhibitors an imperative goal. The last decade has seen an abundance of clinical trials using these drugs alone or in combination with chemotherapy. This culminated with the recent approval by the US Food and Drug Administration of Midostaurin for the treatment of FLT3-mutated AML. Initial success has been followed by the emergence of clinical resistance. Although novel FLT3 inhibitors are being developed, studies into mechanisms of resistance raise hope of new strategies to prevent emergence of resistance and eliminate minimal residual disease.

Indexed as

Drug Resistance, NeoplasmAntineoplastic AgentsBone MarrowCell SurvivalCellular Microenvironmentfms-Like Tyrosine Kinase 3Gene DuplicationHumansLeukemia, Myeloid, AcuteMutationProtein Kinase InhibitorsSignal TransductionTandem Repeat SequencesAntineoplastic Agentsfms-Like Tyrosine Kinase 3Protein Kinase InhibitorsAMLFLT3 inhibitorsFLT3-ITDStem cell niche

Identifiers

PMID28673395
PMCPMC5512588
OpenAlexW2614211938

What OpenQuestion holds

Textmetadata
LicenceTDM
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.