Evidence map›Paper›PMID 41076459›Full record

ArticleActa neuropathologica2025

Molecular characterization and clinical features of diffuse midline glioma in the pediatric precision oncology registry INFORM.

Elke Pfaff, Kathrin Schramm, Mirjam Blattner-Johnson, Barbara C Jones, Sebastian Stark, Gnana Prakash Balasubramanian, Christopher Previti, Robert J Autry, Petra Fiesel, Felix Sahm and 23 more

Abstract read
In one paragraph

Article in Acta neuropathologica, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

33 authors.

Elke PfaffHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
Kathrin SchrammHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
Mirjam Blattner-JohnsonHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
Barbara C JonesHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
Sebastian StarkHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
Gnana Prakash BalasubramanianHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
Christopher PrevitiHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
Robert J AutryHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
Petra FieselDepartment of Neuropathology, Institute of Pathology, Heidelberg University Hospital, Heidelberg, Germany.
Felix SahmDepartment of Neuropathology, Institute of Pathology, Heidelberg University Hospital, Heidelberg, Germany.
David ReussDepartment of Neuropathology, Institute of Pathology, Heidelberg University Hospital, Heidelberg, Germany.
Andreas von DeimlingDepartment of Neuropathology, Institute of Pathology, Heidelberg University Hospital, Heidelberg, Germany.
Cornelis M van TilburgHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
Kristian W PajtlerHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
Till MildeHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
Uta DirksenPediatrics III, West German Cancer Centre Essen, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
Christof M KrammDivision of Pediatric Hematology and Oncology, University Medical Center Goettingen, Göttingen, Germany.
André O von BuerenDivision of Pediatric Hematology and Oncology, Department of Pediatrics, Gynecology and Obstetrics, University Hospital of Geneva, Geneva, Switzerland.
Caroline HutterDepartment of Pediatrics and Adolescent Medicine, St. Anna Children's Hospital, Medical University of Vienna, Vienna, Austria.
Bram de WildePediatric Hematology and Oncology, Ghent University Hospital, Ghent, Belgium.
Jan MolenaarPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Nicolas U GerberDepartment of Oncology and Children's Research Center, University Children's Hospital Zurich, Eleonoren Foundation, Zurich, Switzerland.
Olli LohiFaculty of Medicine and Health Technology, Tampere Center for Child, Adolescent and Maternal Health Research, Tampere University, Tampere, Finland.
Monica C Munthe-KaasDepartment of Pediatric Oncology and Hematology, Oslo University Hospital, Oslo, Norway.
Kleopatra GeorgantziChildhood Cancer Research Unit, Department of Women's and Children's Health, Karolinska Institute, Stockholm, Sweden.
Bernarda KazanowskaDepartment of Pediatric Hematology/Oncology and BMT, University of Wroclaw, Wrocław, Poland.
Michal ZápotockýCenter for Pediatric Neuro-Oncology, Motol University Hospital, Prague, Czech Republic.
Antonis KattamisDivision of Pediatric Hematology-Oncology, First Department of Pediatrics, "Aghia Sophia" Children's Hospital, National and Kapodistrian University of Athens, Athens, Greece.
Maria FilippidouDivision of Pediatric Hematology-Oncology, First Department of Pediatrics, "Aghia Sophia" Children's Hospital, National and Kapodistrian University of Athens, Athens, Greece.
Iris FriedPediatric Hemato-Oncology Unit, Wilf Children's Hospital, Shaare Zedek Medical Center, Jerusalem, Israel.
Stefan M PfisterHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
Olaf WittHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
David T W JonesHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany. david.jones@kitz-heidelberg.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diffuse midline glioma (DMG; a subtype of pediatric high-grade glioma) is a fatal disease in children, due to the localization in critical structures of the central nervous system, its invasive nature, and limited treatment options. Molecularly, DMG with loss of histone 3 K27 trimethylation (mostly through the typical K27M-mutation in histone 3) have been relatively well characterized, however, no unambiguous Achilles' heel for targeted therapeutic approaches could be identified to date. This study integrates detailed molecular characteristics of pediatric DMGs with clinical data in a large, international cohort in order to contribute to a better understanding necessary for further development of therapeutic approaches. A total of 162 DMG tumors were analyzed within the INFORM registry from 01/2015 to 11/2023 using comprehensive molecular profiling (including exome, whole-genome and RNA next-generation sequencing approaches, complemented with DNA methylation analysis). Molecular results were correlated with clinical data of the respective patients including the treatment regimen applied and patients' outcomes. This well-defined cohort of histone 3 K27-altered DMG according to the current WHO classification showed typical molecular alterations for this entity, with differences in frequencies in specific subgroups. The presence of TP53 mutation and the absence of MAPK pathway alteration in the tumors were associated with worse outcomes. In a substantial proportion of patients, genetic alterations serving as targets for potential therapeutic approaches could be identified. This large, international, prospective DMG cohort combines comprehensive molecular characterization of the tumors with registry-level clinical data, thereby contributing to a better understanding of the underlying tumor biology, potential prognostic and predictive markers and the potential impact of targeted therapies.

Indexed as

Brain NeoplasmsGliomaAdolescentChildChild, PreschoolCohort StudiesDNA MethylationFemaleHistonesHumansInfantMaleMutationPrecision MedicineRegistriesHistonesMolecular characterizationPediatric diffuse midline gliomaPredictive and prognostic markersTargeted therapy

Identifiers

PMID41076459
PMCPMC12515216

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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.