Evidence map›Paper›PMID 40055259›Full record

ArticleJournal of neuro-oncology2025

Extra-central nervous system metastasis from high-grade glioma: a single-institution experience.

Christina Abi Faraj, Ian E McCutcheon, Maria A Gubbiotti, Subha Perni, Maria K Gule-Monroe, Kadir Akdemir, Victoria E Clark, Evan D Bander, Monica E Loghin, Sujit S Prabhu and 2 more

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Article in Journal of neuro-oncology, 2025. 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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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

12 authors.

Christina Abi FarajDepartment of Neurosurgery, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.ORCID http://orcid.org/0000-0002-6441-4291
Ian E McCutcheonDepartment of Neurosurgery, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
Maria A GubbiottiDepartment of Neuropathology, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
Subha PerniDepartment of Radiation Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
Maria K Gule-MonroeDepartment of Neuroradiology, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
Kadir AkdemirDepartment of Neurosurgery, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
Victoria E ClarkDepartment of Neurosurgery, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
Evan D BanderDepartment of Neurosurgery, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
Monica E LoghinDepartment of Neuro-Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
Sujit S PrabhuDepartment of Neurosurgery, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
Frederick F LangDepartment of Neurosurgery, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
Jeffrey S WeinbergDepartment of Neurosurgery, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA. jweinberg@mdanderson.org.ORCID http://orcid.org/0000-0001-5587-6673

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeExtra-central nervous system metastasis (ECM) from glioblastoma and other high-grade gliomas (HGGs) is exceedingly rare, likely due to central nervous system barriers and the short overall survival (OS) in HGG patients, limiting the timeframe for metastasis. Improved treatments have extended survival, potentially increasing ECM incidence, though mechanisms remain unclear.

methodsThis retrospective study examines HGG patients (n = 16) with ECM treated at The University of Texas M. D. Anderson Cancer Center from 1993 to 2023.

resultsMedian age at HGG and ECM diagnoses were 33.6 and 35.1 years, respectively, with a slight female predominance. Diagnoses included glioblastoma, IDH-wildtype WHO Grade 4 (n = 11), epithelioid glioblastoma WHO Grade 4 (n = 2), astrocytoma IDH-mutant WHO Grade 4 (n = 2), and H3K27-altered diffuse midline glioma (n = 1). Median interval from HGG to ECM diagnosis was 10 months. The temporal lobe was the most common HGG site, with ECM primarily in cervical lymph nodes, bone, parotid gland, and cranial soft tissues. Genomic profiling identified TP53, EGFR, RB1, NF1, TERT promoter, and BRAF V600E mutations. Median OS from HGG diagnosis was 23.4 months, and median OS following ECM diagnosis was 5.9 months. Chemotherapy and radiotherapy to ECM sites extended survival. Leptomeningeal disease was present in 50% of cases and correlated with worse prognosis. ECM typically developed in advanced disease stages.

conclusionThis study highlights genomic alterations, management, and outcomes associated with ECM in HGG. Tumor spread may stem from neurosurgical manipulation and occur via hematogenous and/or lymphatic routes. Multimodal treatment extends survival. Targeted therapies based on molecular profiles should be explored.

Indexed as

Brain NeoplasmsGliomaAdolescentAdultAgedFemaleFollow-Up StudiesHumansMaleMiddle AgedMutationNeoplasm GradingPrognosisRetrospective StudiesSurvival RateYoung AdultDiffuse midline gliomaExtra-central nervous system metastasisGlioblastomaHigh-grade glioma

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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.