Evidence map›Paper›PMID 36505804›Full record

ArticleFrontiers in oncology2022

The transcriptomic landscape of elderly acute myeloid leukemia identifies

Sara Villar, Beñat Ariceta, Xabier Agirre, Aura Daniela Urribarri, Rosa Ayala, David Martínez-Cuadrón, Juan Miguel Bergua, Susana Vives, Lorenzo Algarra, Mar Tormo and 11 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. 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

21 authors at 13 institutions in 1 country.

Sara VillarServicio de Hematología y Terapia Celular, Clínica Universidad de Navarra, Instituto de Investigación Sanitaria de Navarra (IDISNA), Pamplona, Spain.
Beñat AricetaCIBERONC Centro de Investigación Biomédica en Red de Cáncer, Pamplona, Spain.
Xabier AgirreCIBERONC Centro de Investigación Biomédica en Red de Cáncer, Pamplona, Spain.
Aura Daniela UrribarriNavarrabiomed, Fundación Miguel Servet, Pamplona, Spain.
Rosa AyalaHospital Universitario 12 de octubre, Madrid, Spain.
David Martínez-CuadrónHospital Universitario y Politécnico la Fe, Valencia, Spain.
Juan Miguel BerguaHospital San Pedro de Alcántara, Cáceres, Spain.
Susana VivesICO Badalona- Hospital Germans Trias i Pujol, Badalona, Spain.
Lorenzo AlgarraHospital General de Albacete, Albacete, Spain.
Mar TormoHospital Clínico Universitario de Valencia, Valencia, Spain.
Pilar MartínezHospital Universitario 12 de octubre, Madrid, Spain.
Josefina SerranoHospital Universitario Reina Sofía, Córdoba, Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Córdoba, Spain.
Catia SimoesProgram of Hematology-Oncology, CIMA, Universidad de Navarra, Pamplona, Spain.
Pilar HerreraHospital Universitario Ramón y Cajal, Madrid, Spain.
Maria José CalasanzCIBERONC Centro de Investigación Biomédica en Red de Cáncer, Pamplona, Spain.
Ana Alfonso-PiérolaServicio de Hematología y Terapia Celular, Clínica Universidad de Navarra, Instituto de Investigación Sanitaria de Navarra (IDISNA), Pamplona, Spain.
Bruno PaivaServicio de Hematología y Terapia Celular, Clínica Universidad de Navarra, Instituto de Investigación Sanitaria de Navarra (IDISNA), Pamplona, Spain.
Joaquín Martínez-LópezHospital Universitario 12 de octubre, Madrid, Spain.
Jesús F San MiguelServicio de Hematología y Terapia Celular, Clínica Universidad de Navarra, Instituto de Investigación Sanitaria de Navarra (IDISNA), Pamplona, Spain.
Felipe PrósperServicio de Hematología y Terapia Celular, Clínica Universidad de Navarra, Instituto de Investigación Sanitaria de Navarra (IDISNA), Pamplona, Spain.
Pau MontesinosHospital Universitario y Politécnico la Fe, Valencia, Spain.
Clinica Universidad de Navarra · ESHospital Universitario 12 De Octubre · ESUniversidad de Navarra · ESHospital Universitari i Politècnic La Fe · ESCentro de Investigación Biomédica en Red de Cáncer · ESHospital Clínico Universitario de Valencia · ESHospital General Universitario de Albacete · ESHospital San Pedro de Alcántara · ESHospital Universitari Germans Trias i Pujol · ESHospital Universitario Ramón y Cajal · ESInstituto Maimónides de Investigación Biomédica de Córdoba · ESNavarrabiomed · ESNavarre Institute of Health Research · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute myeloid leukemia (AML) in the elderly remains a clinical challenge, with a five-year overall survival rate below 10%. The current ELN 2017 genetic risk classification considers cytogenetic and mutational characteristics to stratify fit AML patients into different prognostic groups. However, this classification is not validated for elderly patients treated with a non-intensive approach, and its performance may be suboptimal in this context. Indeed, the transcriptomic landscape of AML in the elderly has been less explored and it might help stratify this group of patients. In the current study, we analyzed the transcriptome of 224 AML patients > 65 years-old at diagnosis treated in the Spanish PETHEMA-FLUGAZA clinical trial in order to identify new prognostic biomarkers in this population. We identified a specific transcriptomic signature for high-risk patients with mutated

Indexed as

acute myeloid leukemiabiomarkerselderlyprognosistranscriptomics

Identifiers

PMID36505804
PMCPMC9729799
OpenAlexW4309845490

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.