Evidence map›Paper›PMID 32246042›Full record

ArticleScientific reports2020

Analysis of SNP Array Abnormalities in Patients with DE NOVO Acute Myeloid Leukemia with Normal Karyotype.

Mariam Ibáñez, Esperanza Such, Esther Onecha, Inés Gómez-Seguí, Alessandro Liquori, Jorge Sellés, David Hervás-Marín, Eva Barragán, Rosa Ayala, Marta LLop and 14 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

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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

24 authors at 7 institutions in 1 country.

Mariam IbáñezHematology Service, Hospital Universitario y Politécnico La Fe, Valencia, Spain.ORCID http://orcid.org/0000-0002-7486-4659
Esperanza SuchHematology Service, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
Esther OnechaHospital 12 de Octubre, Madrid, Spain.
Inés Gómez-SeguíHematology Service, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
Alessandro LiquoriCentro de Investigación Biomédica en Red de Cáncer, Madrid, Spain.ORCID http://orcid.org/0000-0002-4842-5986
Jorge SellésArray's Unit. Instituto Investigación Sanitaria Fundación La Fe, Valencia, Spain.
David Hervás-MarínBiostadistic Unit. Instituto Investigación Sanitaria Fundación La Fe, Valencia, Spain.ORCID http://orcid.org/0000-0003-0635-4961
Eva BarragánCentro de Investigación Biomédica en Red de Cáncer, Madrid, Spain.
Rosa AyalaHospital 12 de Octubre, Madrid, Spain.
Marta LLopCentro de Investigación Biomédica en Red de Cáncer, Madrid, Spain.
María López-PavíaHematology Service, Hospital General, Valencia, Spain.
Inmaculada RapadoHospital 12 de Octubre, Madrid, Spain.
Alex NeefGrupo de Investigación en Hematología, IIS La Fe, Valencia, Spain.
Alejandra Sanjuan-PlaGrupo de Investigación en Hematología, IIS La Fe, Valencia, Spain.
Claudia SargasGrupo de Investigación en Hematología, IIS La Fe, Valencia, Spain.
Elisa Gonzalez-RomeroCentro de Investigación Biomédica en Red de Cáncer, Madrid, Spain.
Mireia Boluda-NavarroGrupo de Investigación en Hematología, IIS La Fe, Valencia, Spain.
Rafa AndreuHematology Service, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
Leonor SenentHematology Service, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
Pau MontesinosHematology Service, Hospital Universitario y Politécnico La Fe, Valencia, Spain.ORCID http://orcid.org/0000-0002-3275-5593
Joaquín Martínez-LópezHospital 12 de Octubre, Madrid, Spain.
Miguel Angel SanzHematology Service, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
Guillermo SanzHematology Service, Hospital Universitario y Politécnico La Fe, Valencia, Spain.ORCID http://orcid.org/0000-0002-2767-8191
José CerveraHematology Service, Hospital Universitario y Politécnico La Fe, Valencia, Spain. cervera_jos@gva.es.
Hospital Universitari i Politècnic La Fe · ESInstituto de Investigación Sanitaria La Fe · ESCentro de Investigación Biomédica en Red de Cáncer · ESResearch Institute Hospital 12 de Octubre · ESUniversidad Cardenal Herrera CEU · ESHospital General Universitario De Valencia · ESUniversitat de València · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nearly 50% of patients with de novo acute myeloid leukemia (AML) harbor an apparently normal karyotype (NK) by conventional cytogenetic techniques showing a very heterogeneous prognosis. This could be related to the presence of cryptic cytogenetic abnormalities (CCA) not detectable by conventional methods. The study of copy number alterations (CNA) and loss of heterozygozity (LOH) in hematological malignancies is possible using a high resolution SNP-array. Recently, in clinical practice the karyotype study has been complemented with the identification of point mutations in an increasing number of genes. We analyzed 252 de novo NK-AML patients from Hospital La Fe (n = 44) and from previously reported cohorts (n = 208) to identify CCA by SNP-array, and to integrate the analysis of CCA with molecular alterations detected by Next-Generation-sequencing. CCA were detected in 58% of patients. In addition, 49% of them harbored CNA or LOH and point mutations, simultaneously. Patients were grouped in 3 sets by their abnormalities: patients carrying several CCA simultaneously, patients with mutations in FLT3, NPM1 and/or DNMT3A and patients with an amalgam of mutations. We found a negative correlation between the number of CCA and the outcome of the patients. This study outlines that CCA are present in up to 50% of NK-AML patients and have a negative impact on the outcome. CCA may contribute to the heterogeneous prognosis.

Indexed as

Chromosome AberrationsPolymorphism, Single NucleotideAdultAgedAged, 80 and overDNA Copy Number VariationsFemaleFollow-Up StudiesHigh-Throughput Nucleotide SequencingHumansKaryotypeLeukemia, Myeloid, AcuteLoss of HeterozygosityMaleMiddle AgedNucleophosminNucleophosmin

Identifiers

PMID32246042
PMCPMC7125150
OpenAlexW3014550245

What OpenQuestion holds

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LicenceCC BY
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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.