Evidence map›Paper›PMID 38507506›Full record

ArticleNeuro-oncology2024

Insights from a multicenter study on adult H3 K27M-mutated glioma: Surgical resection's limited influence on overall survival, ATRX as molecular prognosticator.

Alice Ryba, Zeynep Özdemir, Nitzan Nissimov, Lisa Hönikl, Nicolas Neidert, Martin Jakobs, Darius Kalasauskas, Aleksandrs Krigers, Claudius Thomé, Christian F Freyschlag and 14 more

Abstract readMulticenter Study
In one paragraph

Article in Neuro-oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors.

Alice RybaDepartment of Neurosurgery, Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-0130-8838
Zeynep ÖzdemirDepartment of Neurosurgery, University Hospital of Münster, Münster, Germany.
Nitzan NissimovDepartment of Neurosurgery, Charité University Hospital Berlin, Berlin, Germany.
Lisa HöniklDepartment of Neurosurgery, Technical University Munich, Munich, Germany.
Nicolas NeidertDepartment of Neurosurgery, Charité University Hospital Berlin, Berlin, Germany.
Martin JakobsDepartment of Neurosurgery, Heidelberg University Hospital, Heidelberg, Germany.
Darius KalasauskasDepartment of Neurosurgery, University Medical Center Mainz, Mainz, Germany.
Aleksandrs KrigersDepartment of Neurosurgery, Medical University of Innsbruck, Innsbruck, Austria.
Claudius ThoméDepartment of Neurosurgery, Medical University of Innsbruck, Innsbruck, Austria.
Christian F FreyschlagDepartment of Neurosurgery, Medical University of Innsbruck, Innsbruck, Austria.
Florian RingelDepartment of Neurosurgery, University Medical Center Mainz, Mainz, Germany.
Andreas UnterbergDepartment of Neurosurgery, Heidelberg University Hospital, Heidelberg, Germany.
Philip Dao TrongDepartment of Neurosurgery, Heidelberg University Hospital, Heidelberg, Germany.
Jürgen BeckDepartment of Neurosurgery, Medical Center - University of Freiburg, Freiburg, Germany.
Dieter Henrik HeilandDepartment of Neurosurgery, Medical Center - University of Freiburg, Freiburg, Germany.
Bernhard MeyerDepartment of Neurosurgery, Technical University Munich, Munich, Germany.
Peter VajkoczyDepartment of Neurosurgery, Charité University Hospital Berlin, Berlin, Germany.
Julia OnkenDepartment of Neurosurgery, Charité University Hospital Berlin, Berlin, Germany.
Walter StummerDepartment of Neurosurgery, University Hospital of Münster, Münster, Germany.ORCID 0000-0002-3460-0640
Eric Suero MolinaDepartment of Neurosurgery, University Hospital of Münster, Münster, Germany.
Jens GemptDepartment of Neurosurgery, Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Manfred WestphalDepartment of Neurosurgery, Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0003-3483-6335
Ulrich SchüllerInstitute of Neuropathology, Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-8731-1121
Malte MohmeDepartment of Neurosurgery, Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0003-0627-9092

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundH3 K27M-mutated gliomas were first described as a new grade 4 entity in the 2016 World Health Organization classification. Current studies have focused on its typical appearance in children and young adults, increasing the need to better understand the prognostic factors and impact of surgery on adults. Here, we report a multicentric study of this entity in adults.

methodsWe included molecularly confirmed H3 K27M-mutated glioma cases in patients ≥ 18 years diagnosed between 2016 and 2022. Clinical, radiological, and surgical features were analyzed. Univariate and multivariate analyses were performed to identify prognostic factors.

resultsAmong 70 patients with a mean age of 36.1 years, the median overall survival (OS) was 13.6 ± 14 months. Gross-total resection was achieved in 14.3% of patients, whereas 30% had a subtotal resection and 54.3% a biopsy. Tumors located in telencephalon/diencephalon/myelencephalon were associated with a poorer OS, while a location in the mesencephalon/metencephalon showed a significantly longer OS (8.7 vs. 25.0 months, P = .007). Preoperative Karnofsky-Performance Score (KPS) ≤ 80 showed a reduced OS (4.2 vs. 18 months, P = .02). Furthermore, ATRX loss, found in 25.7%, was independently associated with an increased OS (31 vs. 8.3 months, P = .0029). Notably, patients undergoing resection showed no survival benefit over biopsy (12 vs. 11 months, P = .4006).

conclusionsThe present study describes surgical features of H3 K27M-mutated glioma in adulthood in a large multicentric study. Our data reveal that ATRX status, location and KPS significantly impact OS in H3 K27M-mutated glioma. Importantly, our dataset indicates that resection does not offer a survival advantage over biopsy.

Indexed as

Brain NeoplasmsGliomaHistonesMutationX-linked Nuclear ProteinAdolescentAdultAgedBiomarkers, TumorFemaleFollow-Up StudiesHumansMaleMiddle AgedPrognosisRetrospective StudiesATRX protein, humanBiomarkers, TumorHistonesX-linked Nuclear ProteinH3F3AH3 K27Mhigh-grade gliomaHIST1H3BHistone H3

Identifiers

PMID38507506
PMCPMC11300017

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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.