Evidence map›Paper›PMID 25145428›Full record

ReviewFuture oncology (London, England)2014

Quizartinib for the treatment of FLT3/ITD acute myeloid leukemia.

Mark Levis

Open access · greenAbstract readReview
In one paragraph

Review in Future oncology (London, England), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

39 citing papers in PubMed, 61 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Accelerating CAR-T Cell Therapies with Small-Molecule Inhibitors.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2025
    Review
  9. Molecular medicine reports · 2024
    Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Cancers · 2022
    Article
  15. Which FLT3 Inhibitor for Treatment of AML?Current treatment options in oncology · 2022
    Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. Cutting Edge Molecular Therapy for Acute Myeloid Leukemia.International journal of molecular sciences · 2020
    Review
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

1 author at 1 institution in 1 country.

Mark Levis
Sidney Kimmel Comprehensive Cancer Center · US

Funding

University of Texas M.D. Anderson Cancer SPORE-LeukemiaP50CA100632 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KONOPLEVA, MARINA Y · 2003 to 2023
$43.7M
NCI NIH HHS P50 CA100632NCI NIH HHS P50 CA100632-13
6 · The paper itself

Abstract

FLT3/ITD acute myeloid leukemia is a poor prognosis disease driven by a constitutively activated receptor tyrosine kinase, making it an obvious target for drug development. The development of clinically effective FLT3 inhibitors has been slow, in part because many are multi-targeted inhibitors that are not selective or specific for FLT3. Quizartinib is the first small molecule FLT3 tyrosine kinase inhibitor expressly developed as a FLT3 inhibitor. It is potent, selective and has ideal pharmacokinetics in comparison to other compounds previously tested. This article summarizes its advantages and limitations, and details the insights into the biology of the disease that have been uncovered through the laboratory and clinical use of quizartinib.

Indexed as

Antineoplastic AgentsBenzothiazolesClinical Trials as Topicfms-Like Tyrosine Kinase 3HumansLeukemia, Myeloid, AcuteMutagenesis, InsertionalPhenylurea CompoundsTreatment OutcomeAntineoplastic AgentsBenzothiazolesFLT3 protein, humanfms-Like Tyrosine Kinase 3Phenylurea Compoundsquizartinibc-KITFLT3kinaseleukemiaquizartinib

Identifiers

PMID25145428
PMCPMC6081740
OpenAlexW2015611645

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.