Evidence map›Paper›PMID 38326661›Full record

ArticleJournal of neuro-oncology2024

Treatment outcome of IDH1/2 wildtype CNS WHO grade 4 glioma histologically diagnosed as WHO grade II or III astrocytomas.

Naureen Keric, Harald Krenzlin, Darius Kalasauskas, Christian F Freyschlag, Oliver Schnell, Martin Misch, Christian von der Brelie, Jens Gempt, Aleksandrs Krigers, Arthur Wagner and 10 more

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in Journal of neuro-oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

6 citing papers in PubMed, 4 citations in OpenAlex.

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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

20 authors at 6 institutions in 2 countries.

Naureen KericDepartment of Neurosurgery, University Medical Center Mainz, Johannes Gutenberg University of Mainz, Langenbeckstr. 1, 55131, Mainz, Germany. Naureen.keric@unimedizin-mainz.de.ORCID http://orcid.org/0000-0001-8457-0059
Harald KrenzlinDepartment of Neurosurgery, University Medical Center Mainz, Johannes Gutenberg University of Mainz, Langenbeckstr. 1, 55131, Mainz, Germany.
Darius KalasauskasDepartment of Neurosurgery, University Medical Center Mainz, Johannes Gutenberg University of Mainz, Langenbeckstr. 1, 55131, Mainz, Germany.
Christian F FreyschlagDepartment of Neurosurgery, Medical University of Innsbruck, Innsbruck, Austria.
Oliver SchnellDepartment of Neurosurgery, Medical Center University of Freiburg, Freiburg, Germany.
Martin MischDepartment of Neurosurgery, Charité University Berlin, Berlin, Germany.
Christian von der BrelieDepartment of Neurosurgery, University Medical Center Göttingen, Göttingen, Germany.
Jens GemptDepartment of Neurosurgery, Technical University Munich, Munich, Germany.
Aleksandrs KrigersDepartment of Neurosurgery, Medical University of Innsbruck, Innsbruck, Austria.
Arthur WagnerDepartment of Neurosurgery, Technical University Munich, Munich, Germany.
Felipa LangeDepartment of Neurosurgery, University Medical Center Mainz, Johannes Gutenberg University of Mainz, Langenbeckstr. 1, 55131, Mainz, Germany.
Dorothee MielkeDepartment of Neurosurgery, University Medical Center Göttingen, Göttingen, Germany.
Clemens SommerInstitute of Neuropathology, University Medical Center Mainz, Mainz, Germany.
Marc A BrockmannDepartment of Neuroradiology, University Medical Center Mainz, Mainz, Germany.
Bernhard MeyerDepartment of Neurosurgery, Technical University Munich, Munich, Germany.
Veit RohdeDepartment of Neurosurgery, University Medical Center Göttingen, Göttingen, Germany.
Peter VajkoczyDepartment of Neurosurgery, Charité University Berlin, Berlin, Germany.
Jürgen BeckDepartment of Neurosurgery, Medical Center University of Freiburg, Freiburg, Germany.
Claudius ThoméDepartment of Neurosurgery, Medical University of Innsbruck, Innsbruck, Austria.
Florian RingelDepartment of Neurosurgery, University Medical Center Mainz, Johannes Gutenberg University of Mainz, Langenbeckstr. 1, 55131, Mainz, Germany.
Johannes Gutenberg University Mainz · DEInnsbruck Medical University · ATTechnical University of Munich · DEUniversitätsmedizin Göttingen · DECharité - Universitätsmedizin Berlin · DEUniversity of Freiburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIsocitrate dehydrogenase (IDH)1/2 wildtype (wt) astrocytomas formerly classified as WHO grade II or III have significantly shorter PFS and OS than IDH mutated WHO grade 2 and 3 gliomas leading to a classification as CNS WHO grade 4. It is the aim of this study to evaluate differences in the treatment-related clinical course of these tumors as they are largely unknown.

methodsPatients undergoing surgery (between 2016-2019 in six neurosurgical departments) for a histologically diagnosed WHO grade 2-3 IDH1/2-wt astrocytoma were retrospectively reviewed to assess progression free survival (PFS), overall survival (OS), and prognostic factors.

resultsThis multi-center study included 157 patients (mean age 58 years (20-87 years); with 36.9% females). The predominant histology was anaplastic astrocytoma WHO grade 3 (78.3%), followed by diffuse astrocytoma WHO grade 2 (21.7%). Gross total resection (GTR) was achieved in 37.6%, subtotal resection (STR) in 28.7%, and biopsy was performed in 33.8%. The median PFS (12.5 months) and OS (27.0 months) did not differ between WHO grades. Both, GTR and STR significantly increased PFS (P < 0.01) and OS (P < 0.001) compared to biopsy. Treatment according to Stupp protocol was not associated with longer OS or PFS compared to chemotherapy or radiotherapy alone. EGFR amplification (P = 0.014) and TERT-promotor mutation (P = 0.042) were associated with shortened OS. MGMT-promoter methylation had no influence on treatment response.

conclusionsWHO grade 2 and 3 IDH1/2 wt astrocytomas, treated according to the same treatment protocols, have a similar OS. Age, extent of resection, and strong EGFR expression were the most important treatment related prognostic factors.

Indexed as

AstrocytomaBrain NeoplasmsGliomaErbB ReceptorsFemaleHumansIsocitrate DehydrogenaseMaleMiddle AgedMutationPrognosisRetrospective StudiesTreatment OutcomeWorld Health OrganizationErbB ReceptorsIDH1 protein, humanIsocitrate DehydrogenaseExtend of resectionGlioblastomaIDH1/2 wildtypePrognostic factorsWHO grade II or III astrocytomas

Identifiers

PMID38326661
PMCPMC10978634
OpenAlexW4391594854

What OpenQuestion holds

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Registered trials

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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.