Evidence map›Paper›PMID 34671057›Full record

ArticleScientific reports2021

Prognostic significance of FLT3-ITD length in AML patients treated with intensive regimens.

Tamara Castaño-Bonilla, Juan M Alonso-Dominguez, Eva Barragán, Rebeca Rodríguez-Veiga, Claudia Sargas, Cristina Gil, Carmen Chillón, María B Vidriales, Raimundo García, Joaquín Martínez-López and 26 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
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  6. Molecular medicine reports · 2024
    Article
  7. Review
  8. Recent advances in CAR-T cell therapy for acute myeloid leukaemia.Journal of cellular and molecular medicine · 2024
    Review
  9. Review
  10. Shift of N-MYC Oncogene Expression in AML Patients Carrying the FLT3-ITD Mutation.Pathophysiology : the official journal of the International Society for Pathophysiology · 2023
    Article
  11. Article
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  13. Article
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  15. Review
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  18. No Evidence thatDisease markers · 2022
    Article
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

36 authors at 20 institutions in 1 country.

Tamara Castaño-BonillaHematology Department, Hospital Universitario Fundación Jiménez Díaz, Avenida Reyes Católicos, 2, 28040, Madrid, Spain.
Juan M Alonso-DominguezHematology Department, Hospital Universitario Fundación Jiménez Díaz, Avenida Reyes Católicos, 2, 28040, Madrid, Spain. juan.adominguez@fjd.es.ORCID 0000-0001-6233-5912
Eva BarragánHematology Department, Hospital Universitario La Fe de Valencia, Valencia, Spain.
Rebeca Rodríguez-VeigaHematology Department, Hospital Universitario La Fe de Valencia, Valencia, Spain.
Claudia SargasHematology Department, Hospital Universitario La Fe de Valencia, Valencia, Spain.
Cristina GilHematology Department, Hospital General de Alicante, Alicante, Spain.
Carmen ChillónHematology Department, Hospital Universitario de Salamanca, Salamanca, Spain.
María B VidrialesHematology Department, Hospital Universitario de Salamanca, Salamanca, Spain.
Raimundo GarcíaHematology Department, Hospital General de Castellón, Castellón, Spain.
Joaquín Martínez-LópezHematology Department, Hospital Universitario Doce de Octubre, Complutense University, CNIO, Madrid, Spain.
Rosa AyalaHematology Department, Hospital Universitario Doce de Octubre, Complutense University, CNIO, Madrid, Spain.
María J LarrayozMolecular Biology Department, Cimalab Diagnosis, Clínica Universitaria de Navarra, Navarra, Spain.
Eduardo AnguitaHematology Department, Hospital Universitario Clínico San Carlos, Medicine Department, UCM, Madrid, Spain.
Rebeca CuelloHematology Department, Hospital Universitario de Valladolid, Valladolid, Spain.
Alberto CantalapiedraHematology Department, Hospital Universitario Río Hortega, Valladolid, Spain.
Estrella CarrilloHematology Department, Hospital Universitario Virgen del Rocío, Instituto de Biomedicina de Sevilla (IBIS/CISC/CIBERON), Sevilla, Spain.
Elena Soria-SaldiseHematology Department, Hospital Universitario Virgen del Rocío, Instituto de Biomedicina de Sevilla (IBIS/CISC/CIBERON), Sevilla, Spain.
Jorge LabradorHematology Department, Hospital Universitario de Burgos, Burgos, Spain.
Isabel RecioHematology Department, Hospital Ntra. Sra. de Sonsoles de Ávila-Complejo Asistencial Ávila, Ávila, Spain.
Lorenzo AlgarraHematology Department, Hospital General de Albacete, Albacete, Spain.
Carlos Rodríguez-MedinaHematology Department, Hospital Universitario de Gran Canaria Doctor Negrín, Las Palmas de Gran Canaria, Spain.
Cristina Bilbao-SyeiroHematology Department, Hospital Universitario de Gran Canaria Doctor Negrín, Las Palmas de Gran Canaria, Spain.
Juan A López-LópezHematology Department, Hospital General Ciudad de Jaén, Jaén, Spain.
Josefina SerranoUGC de Hematologia, Hospital U. Reina Sofia, IMIBIC, UCO, Cordoba, Córdoba, Spain.
Erik De CaboHematology Department, Hospital Comarcal del Bierzo, León, Spain.
María J SayasHematology Department, Hospital Universitario Doctor Peset, Valencia, Spain.
María T OlaveHematology Department, Hospital Clínico Universitario Lozano Blesa, Zaragoza, Spain.
Joaquín Sánchez-GarcíaUGC de Hematologia, Hospital U. Reina Sofia, IMIBIC, UCO, Cordoba, Córdoba, Spain.
Mamen MateosHematology Department, Complejo Hospitalario de Navarra, Navarra, Spain.
Carlos BlasHematology Department, Hospital Universitario Fundación Jiménez Díaz, Avenida Reyes Católicos, 2, 28040, Madrid, Spain.
Jose L López-LorenzoHematology Department, Hospital Universitario Fundación Jiménez Díaz, Avenida Reyes Católicos, 2, 28040, Madrid, Spain.
Daniel Lainez-GonzalezInstituto de Investigación Sanitaria (IIS-FJD), Hospital Universitario Fundación Jiménez Díaz, Madrid, Spain.
Juana SerranoInstituto de Investigación Sanitaria (IIS-FJD), Hospital Universitario Fundación Jiménez Díaz, Madrid, Spain.
David Martínez-CuadrónHematology Department, Hospital Universitario La Fe de Valencia, Valencia, Spain.
Miguel A SanzHematology Department, Hospital Universitario La Fe de Valencia, Valencia, Spain.
Pau MontesinosHematology Department, Hospital Universitario La Fe de Valencia, Valencia, Spain.
Instituto de Investigación Sanitaria La Fe · ESHospital Universitario Fundación Jiménez Díaz · ESInstituto Maimónides de Investigación Biomédica de Córdoba · ESComplejo Hospitalario de Salamanca · ESHospital Universitario 12 De Octubre · ESHospital Universitario de Gran Canaria Doctor Negrín · ESInstituto de Biomedicina de Sevilla · ESCatholic University of Ávila · ESComplejo Hospitalario de Jaén · ESComplejo Hospitalario de Navarra · ESHospital Clínico San Carlos · ESHospital Clínico Universitario de Valladolid · ESHospital Clínico Universitario Lozano Blesa · ESHospital El Bierzo · ESHospital General Universitari de Castelló · ESHospital General Universitario de Albacete · ESHospital General Universitario de Alicante Doctor Balmis · ESHospital Universitario de Burgos · ESHospital Universitario Doctor Peset · ESHospital Universitario Río Hortega · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

FLT3-ITD mutations are detected in approximately 25% of newly diagnosed adult acute myeloid leukemia (AML) patients and confer an adverse prognosis. The FLT3-ITD allelic ratio has clear prognostic value. Nevertheless, there are numerous manuscripts with contradictory results regarding the prognostic relevance of the length and insertion site (IS) of the FLT3-ITD fragment. We aimed to assess the prognostic impact of these variables on the complete remission (CR) rates, overall survival (OS) and relapse-free survival (RFS) of AML patients with FLT3-ITDmutations. We studied the FLT3-ITD length of 362 adult AML patients included in the PETHEMA AML registry. We tried to validate the thresholds of ITD length previously published (i.e., 39 bp and 70 bp) in intensively treated AML patients (n = 161). We also analyzed the mutational profile of 118 FLT3-ITD AML patients with an NGS panel of 39 genes and correlated mutational status with the length and IS of ITD. The AUC of the ROC curve of the ITD length for OS prediction was 0.504, and no differences were found when applying any of the thresholds for OS, RFS or CR rate. Only four out of 106 patients had ITD IS in the TKD1 domain. Our results, alongside previous publications, confirm that FLT3-ITD length lacks prognostic value and clinical applicability.

Indexed as

AdolescentAdultAgedAged, 80 and overDisease-Free SurvivalFemalefms-Like Tyrosine Kinase 3HumansLeukemia, Myeloid, AcuteMaleMiddle AgedMutationPrognosisRemission InductionRetrospective StudiesYoung AdultFLT3 protein, humanfms-Like Tyrosine Kinase 3

Identifiers

PMID34671057
PMCPMC8528825
OpenAlexW3205389182

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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.