Evidence map›Paper›PMID 30514344›Full record

ReviewJournal of hematology & oncology2018

FLT3 inhibitors in acute myeloid leukemia.

Mei Wu, Chuntuan Li, Xiongpeng Zhu

Open access · goldAbstract readReview
In one paragraph

Review in Journal of hematology & oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 100 papers.

0numbers the graph read from it
0cells of the map it votes in
100citing papers in PubMed
15.2field-weighted citation impact, top 1% 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

100 citing papers in PubMed, 175 citations in OpenAlex.

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40 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Mei WuDepartment of Hematology, The People's Hospital of Bozhou, Bozhou, 236800, China.
Chuntuan LiDepartment of Hematology, First Hospital of Quanzhou affiliated to Fujian Medical University, Quanzhou, 362000, China.
Xiongpeng ZhuDepartment of Hematology, First Hospital of Quanzhou affiliated to Fujian Medical University, Quanzhou, 362000, China. xiongpengzhu@163.com.ORCID 0000-0003-4698-2276
Fujian Medical University · CNBozhou People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

FLT3 mutations are one of the most common findings in acute myeloid leukemia (AML). FLT3 inhibitors have been in active clinical development. Midostaurin as the first-in-class FLT3 inhibitor has been approved for treatment of patients with FLT3-mutated AML. In this review, we summarized the preclinical and clinical studies on new FLT3 inhibitors, including sorafenib, lestaurtinib, sunitinib, tandutinib, quizartinib, midostaurin, gilteritinib, crenolanib, cabozantinib, Sel24-B489, G-749, AMG 925, TTT-3002, and FF-10101. New generation FLT3 inhibitors and combination therapies may overcome resistance to first-generation agents.

Indexed as

fms-Like Tyrosine Kinase 3HumansLeukemia, Myeloid, AcuteMutationFLT3 protein, humanfms-Like Tyrosine Kinase 3Acute myeloid leukemiaFLT3FMS-like tyrosine kinase 3 inhibitorsMidostaurin

Identifiers

PMID30514344
PMCPMC6280371
OpenAlexW2902063722

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.