Evidence map›Paper›PMID 33817952›Full record

ArticleMolecular oncology2021

FLT3-ITD mutations in acute myeloid leukaemia - molecular characteristics, distribution and numerical variation.

Caroline Engen, Monica Hellesøy, Tim Grob, Adil Al Hinai, Atle Brendehaug, Line Wergeland, Siv Lise Bedringaas, Randi Hovland, Peter J M Valk, Bjørn T Gjertsen

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
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  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. The Clinical Utility ofCurrent oncology (Toronto, Ont.) · 2023
    Article
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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

10 authors at 2 institutions in 1 country.

Caroline EngenDepartment of Clinical Science, Centre for Cancer Biomarkers CCBIO, University of Bergen, Norway.ORCID 0000-0003-0843-3057
Monica HellesøyHaematology Section, Department of Medicine, Haukeland University Hospital, Helse Bergen HF, Norway.ORCID 0000-0002-0115-7427
Tim GrobDepartment of Haematology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Adil Al HinaiDepartment of Haematology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Atle BrendehaugDepartment of Medical Genetics, Haukeland University Hospital, Helse Bergen HF, Norway.
Line WergelandDepartment of Clinical Science, Centre for Cancer Biomarkers CCBIO, University of Bergen, Norway.
Siv Lise BedringaasDepartment of Clinical Science, Centre for Cancer Biomarkers CCBIO, University of Bergen, Norway.
Randi HovlandDepartment of Medical Genetics, Haukeland University Hospital, Helse Bergen HF, Norway.
Peter J M ValkDepartment of Haematology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Bjørn T GjertsenDepartment of Clinical Science, Centre for Cancer Biomarkers CCBIO, University of Bergen, Norway.ORCID 0000-0001-9358-9704
Haukeland University Hospital · NOUniversity of Bergen · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recurrent somatic internal tandem duplications (ITD) in the FMS-like tyrosine kinase 3 (FLT3) gene characterise approximately one third of patients with acute myeloid leukaemia (AML), and FLT3-ITD mutation status guides risk-adapted treatment strategies. The aim of this work was to characterise FLT3-ITD variant distribution in relation to molecular and clinical features, and overall survival in adult AML patients. We performed two parallel retrospective cohort studies investigating FLT3-ITD length and expression by cDNA fragment analysis, followed by Sanger sequencing in a subset of samples. In the two cohorts, a total of 139 and 172 mutant alleles were identified in 111 and 123 patients, respectively, with 22% and 28% of patients presenting with more than one mutated allele. Further, 15% and 32% of samples had a FLT3-ITD total variant allele frequency (VAF) < 0.3, while 24% and 16% had a total VAF ≥ 0.7. Most of the assessed clinical features did not significantly correlate to FLT3-ITD numerical variation nor VAF. Low VAF was, however, associated with lower white blood cell count, while increasing VAF correlated with inferior overall survival in one of the cohorts. In the other cohort, ITD length above 50 bp was identified to correlate with inferior overall survival. Our report corroborates the poor prognostic association with high FLT3-ITD disease burden, as well as extensive inter- and intrapatient heterogeneity in the molecular features of FLT3-ITD. We suggest that future use of FLT3-targeted therapy could be accompanied with thorough molecular diagnostics and follow-up to better predict optimal therapy responders.

Indexed as

Gene DuplicationMutationAdolescentAdultAgedAged, 80 and overFemalefms-Like Tyrosine Kinase 3Gene FrequencyHumansLeukemia, Myeloid, AcuteMaleMiddle AgedRetrospective StudiesSurvival AnalysisYoung AdultFLT3 protein, humanfms-Like Tyrosine Kinase 3acute myeloid leukaemiaFLT3-ITDlength mutationoutcomeprognosis

Identifiers

PMID33817952
PMCPMC8410560
OpenAlexW3145710839

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Registered trials

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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.