Evidence map›Paper›PMID 37403747›Full record

ArticleCancer medicine2023

Incidence and prognostic impact of U2AF1 mutations and other gene alterations in myelodysplastic neoplasms with isolated 20q deletion.

Martín I Castillo, Villamón E Ribate, Calabuig M Muñoz, Sanz G Santillana, Such E Taboada, Mora E Casterá, Calasanz M J Abinzano, Irigoyen A Barranco, Collado R Nieto, Vara M Pampliega and 11 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

3 citing papers in PubMed, 3 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

21 authors at 10 institutions in 1 country.

Martín I CastilloServicio de Hematología, Hospital Clínico Universitario de Valencia, Instituto de Investigación Sanitaria INCLIVA, Valencia, Spain.ORCID 0000-0003-1511-4687
Villamón E RibateServicio de Hematología, Hospital Clínico Universitario de Valencia, Instituto de Investigación Sanitaria INCLIVA, Valencia, Spain.
Calabuig M MuñozServicio de Hematología, Hospital Clínico Universitario de Valencia, Instituto de Investigación Sanitaria INCLIVA, Valencia, Spain.
Sanz G SantillanaServicio de Hematología, Hospital Universitario y Politécnico La Fe, Instituto de Investigación Sanitaria La Fe, CIBERONC - ISCIII, Valencia, Spain.
Such E TaboadaServicio de Hematología, Hospital Universitario y Politécnico La Fe, Instituto de Investigación Sanitaria La Fe, CIBERONC - ISCIII, Valencia, Spain.
Mora E CasteráServicio de Hematología, Hospital Universitario y Politécnico La Fe, Instituto de Investigación Sanitaria La Fe, CIBERONC - ISCIII, Valencia, Spain.
Calasanz M J AbinzanoCIMA LAB Diagnostics, Universidad de Navarra, CIBERONC - ISCIII, Pamplona, Spain.
Irigoyen A BarrancoCIMA LAB Diagnostics, Universidad de Navarra, CIBERONC - ISCIII, Pamplona, Spain.
Collado R NietoServicio de Hematología, Consorcio Hospital General Universitario de Valencia, Valencia, Spain.
Vara M PampliegaServicio de Hematología y Hemoterapia del Hospital Universitario de Cruces, Barakaldo, Spain.
M L BlancoServicio de Hematología, Hospital de la Santa Creu i Sant Pau, Valencia, Spain.
Álvarez S de AndrésNIMGenetics, Genómica y Medicina, Madrid, Spain.
Pérez J de OteyzaServicio de Hematología, Hospital Universitario HM Madrid, Madrid, Spain.
Bernal T Del CastilloServicio de Hematología, Hospital Universidad de Asturias, IISPA, IUOPA, Valencia, Spain.
Granada I FontServicio de Hematología, Hospital Germans Trias i Pujol, Institut Català d'Oncologia, Institut de Recerca contra la Leucèmia Josep Carreras, Universidad Autónoma de Barcelona, CIBERONC - ISCIII, Bellaterra, Spain.
Jerez A CayuelaServicio de Hematología, Hospital Universitario Morales Meseguer, Murcia, Spain.
M Díez-CampeloServicio de Hematología, Hospital Universitario de Salamanca, CIBERONC - ISCIII, Salamanca, Spain.
Abellán R SánchezDepartamento de Bioquímica y Patología Molecular, Hospital Clínico Universitario de Valencia, Instituto de Investigación Sanitaria INCLIVA, Valencia, Spain.
Solano C VercetServicio de Hematología, Hospital Clínico Universitario de Valencia, Instituto de Investigación Sanitaria INCLIVA, Valencia, Spain.
Tormo M DíazServicio de Hematología, Hospital Clínico Universitario de Valencia, Instituto de Investigación Sanitaria INCLIVA, Valencia, Spain.
Grupo Español de Síndromes Mielodisplásicos (GESMD)
Hospital Clínico Universitario de Valencia · ESInstituto de Salud Carlos III · ESComplejo Hospitalario de Salamanca · ESHospital de Cruces · ESHospital de Sant Pau · ESHospital General Universitario De Valencia · ESHospital General Universitario Morales Meseguer · ESHospital Universitario HM Madrid · ESInstituto de Medicina Genómica · ESUniversitat Autònoma de Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn myelodysplastic neoplasms (MDS), the 20q deletion [del(20q)] is a recurrent chromosomal abnormality that it has a high co-occurrence with U2AF1 mutations. Nevertheless, the prognostic impact of U2AF1 in these MDS patients is uncertain and the possible clinical and/or prognostic differences between the mutation type and the mutational burden are also unknown.

methodsOur study analyzes different molecular variables in 100 MDS patients with isolated del(20q). RESULTS &

conclusionsWe describe the high incidence and negative prognostic impact of U2AF1 mutations and other alterations such as in ASXL1 gene to identify prognostic markers that would benefit patients to receive earlier treatment.

Indexed as

Myelodysplastic SyndromesSplicing Factor U2AFHumansIncidenceMutationPrognosisSplicing Factor U2AFU2AF1 protein, human20q deletionmyelodysplastic neoplasmsprognosisquantitative allele-specific PCRU2AF1 mutations

Identifiers

PMID37403747
PMCPMC10501246
OpenAlexW4383187548

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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.