Evidence map›Paper›PMID 42845834›Full record

ArticleFrontiers in oncology2026

Distribution of molecular subtypes in a Colombian cohort of patients with acute lymphoblastic leukemia using whole-transcriptome analysis.

Edward Perez-Arismendi, Natalia Gomez-Lopera, Juan Camilo Villada, Diana Moreno-Garcia, Federico Arroyave-Ossa, Lina Maria Quiroz, Natalia Valencia-Zuluaga, Javier Munoz-Martinez, Alexandra Restrepo-Rincon, Andres Garces-Arias and 1 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Edward Perez-ArismendiGrupo de Investigación Genética Médica, Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia.
Natalia Gomez-LoperaGrupo de Investigación Genética Médica, Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia.
Juan Camilo VilladaServicio de Oncohematología Pediátrica y Trasplante de Médula Ósea, Hospital San Vicente Fundación, Medellín, Colombia.
Diana Moreno-GarciaLaboratorio especializado, Clínica Colsanitas, Bogotá, Colombia.
Federico Arroyave-OssaServicio de Oncología Pediátrica y Trasplante de Médula Ósea, Departamento de Cancerología, Hospital Pablo Tobón Uribe, Medellín, Colombia.
Lina Maria QuirozServicio de Oncología Pediátrica y Trasplante de Médula Ósea, Departamento de Cancerología, Hospital Pablo Tobón Uribe, Medellín, Colombia.
Natalia Valencia-ZuluagaServicio de Oncología Pediátrica y Trasplante de Médula Ósea, Departamento de Cancerología, Hospital Pablo Tobón Uribe, Medellín, Colombia.
Javier Munoz-MartinezServicio de Oncología Pediátrica y Trasplante de Médula Ósea, Departamento de Cancerología, Hospital Pablo Tobón Uribe, Medellín, Colombia.
Alexandra Restrepo-RinconServicio de Oncología Pediátrica y Trasplante de Médula Ósea, Departamento de Cancerología, Hospital Pablo Tobón Uribe, Medellín, Colombia.
Andres Garces-AriasUnidad de Oncología, Hospital Alma Máter de Antioquia, Medellín, Colombia.
Gonzalo Vasquez-PalacioGrupo de Investigación Genética Médica, Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Acute lymphoblastic leukemia (ALL) is a common pediatric malignancy and shows marked genetic heterogeneity. Transcriptomic profiling may improve molecular diagnosis and risk stratification, particularly in admixed Latin American populations. Methods: We characterized the transcriptomic landscape of pediatric ALL in 40 Colombian patients aged <20 years using whole-transcriptome RNA sequencing of diagnostic bone marrow or peripheral blood samples. Bioinformatic analyses enabled molecular subtype assignment, fusion detection, differential expression analysis, and variant calling. Results: The median age was 8 years, and 8 patients had measurable residual disease at the end of induction. The most frequent subtypes were Conclusions: Molecular classification refined conventional risk stratification in 10% of patients, supporting the potential clinical utility of transcriptomic profiling in pediatric ALL.

Indexed as

acute lymphoblastic leukemiadifferential expression analysisgene fusionsmolecular subtypesPh-like ALLRNA-seqsingle nucleotide variantswhole-transcriptome sequencing

Identifiers

PMID42845834
PMCPMC13642327

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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.