Evidence map›Paper›PMID 41567539›Full record

ArticleFrontiers in neurology2025

Integrating molecular profiling into glioma diagnosis: implications of the WHO-CNS5-2021 classification of adult-type diffuse gliomas in Colombian patients.

Omar Echeverría, Andrés Felipe Patiño-Aldana, Ana María Chinchilla, Nora Contreras, Stevan Peralta, Nicolas Caballero, Hanna Valentina Tovar, José Manuel Palacio, Verónica Uribe, Matteo Mineo-Pachón and 6 more

Abstract read
In one paragraph

Article in Frontiers in neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

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

16 authors.

Omar Echeverría *Center for Research in Genetics and Genomics (CIGGUR), School of Medicine and Health Sciences, Institute of Translational Medicine (IMT), Universidad del Rosario, Bogotá, Colombia.
Andrés Felipe Patiño-Aldana *Clinical Research Group, School of Medicine and Health Sciences, Universidad del Rosario, Bogotá, Colombia.
Ana María ChinchillaCenter for Research in Genetics and Genomics (CIGGUR), School of Medicine and Health Sciences, Institute of Translational Medicine (IMT), Universidad del Rosario, Bogotá, Colombia.
Nora ContrerasCenter for Research in Genetics and Genomics (CIGGUR), School of Medicine and Health Sciences, Institute of Translational Medicine (IMT), Universidad del Rosario, Bogotá, Colombia.
Stevan PeraltaCenter for Research in Genetics and Genomics (CIGGUR), School of Medicine and Health Sciences, Institute of Translational Medicine (IMT), Universidad del Rosario, Bogotá, Colombia.
Nicolas CaballeroCenter for Research in Genetics and Genomics (CIGGUR), School of Medicine and Health Sciences, Institute of Translational Medicine (IMT), Universidad del Rosario, Bogotá, Colombia.
Hanna Valentina TovarClinical Research Group, School of Medicine and Health Sciences, Universidad del Rosario, Bogotá, Colombia.
José Manuel PalacioClinical Research Group, School of Medicine and Health Sciences, Universidad del Rosario, Bogotá, Colombia.
Verónica UribeCenter for Research in Genetics and Genomics (CIGGUR), School of Medicine and Health Sciences, Institute of Translational Medicine (IMT), Universidad del Rosario, Bogotá, Colombia.
Matteo Mineo-PachónCenter for Research in Genetics and Genomics (CIGGUR), School of Medicine and Health Sciences, Institute of Translational Medicine (IMT), Universidad del Rosario, Bogotá, Colombia.
Fernando VelandiaConsultant, Bogotá, Colombia.
William Mauricio Riveros CastilloDepartment of Neurosurgery, Hospital Universitario Mayor Méderi and Samaritana University Hospital, School of Medicine and Health Sciences, Universidad del Rosario, Bogotá, Colombia.
Nattaly ValeroDepartment of Molecular Diagnosis, Genética Molecular de Colombia SAS, Bogotá, Colombia.
Daniel Felipe Silgado-GuzmánDepartment of Molecular Diagnosis, Genética Molecular de Colombia SAS, Bogotá, Colombia.
Alejandro Ondo-MendezClinical Research Group, School of Medicine and Health Sciences, Universidad del Rosario, Bogotá, Colombia.
Dora Janeth Fonseca-MendozaCenter for Research in Genetics and Genomics (CIGGUR), School of Medicine and Health Sciences, Institute of Translational Medicine (IMT), Universidad del Rosario, Bogotá, Colombia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Gliomas are the most frequent type of primary malignant central nervous system (CNS) tumors, representing a group of heterogeneous neoplasms with variable clinical behavior that require adequate diagnostic accuracy. The identification of molecular biomarkers has recently gained significance for the diagnosis, prognosis, and treatment of CNS tumors; the application of current clinical guidelines is necessary. Our study performed a molecular characterization of gliomas in a cohort of Colombian patients using the recommendations of the 2021 World Health Organization (WHO) CNS 5 classification. Materials and methods: We analyzed 22 Colombian patients with CNS tumors. Molecular techniques including Sanger sequencing, multiplex ligation-dependent probe amplification (MLPA) and methylation-specific MLPA (MS-MLPA) were used to identify mutations in Results: Our results demonstrated a 23% discordance rate between histopathologic and molecular classifications, with most of the discrepancies due to an initial histopathologic classification of glioblastomas, which were molecularly reclassified as astrocytomas. In addition, molecular profiling allowed us to identify non-canonical mutations, including Discussion: We highlight the importance of incorporating molecular methods to improve diagnostic accuracy and achieve personalized treatments for gliomas, as proposed by the current 2021 WHO CNS 5 tumor classification guidelines. Performing new studies with larger patient cohorts integrating clinical data is necessary to determine the behavior, epidemiology, and therapeutic outcomes of this type of tumor more comprehensively.

Indexed as

1p/19q co-deletionbrain neoplasmsgliomasIDHmutationsTERT promoterWHO CNS5

Identifiers

PMID41567539
PMCPMC12815851

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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.