Evidence map›Paper›PMID 40359980›Full record

ArticleJournal of Korean medical science2025

Radiation-Induced Meningiomas Have an Aggressive Clinical Course: Genetic Signature Is Limited to

Tae-Kyun Kim, Jong Seok Lee, Ji Hoon Phi, Seung Ah Choi, Joo Whan Kim, Chul-Kee Park, Hongseok Yun, Young-Soo Park, Sung-Hye Park, Seung-Ki Kim

Abstract read
In one paragraph

Article in Journal of Korean medical science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

10 authors.

Tae-Kyun Kim *Department of Neurosurgery, Nara Medical University, Nara, Japan.ORCID https://orcid.org/0000-0003-2765-7937
Jong Seok Lee *Department of Neurosurgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-1423-2681
Ji Hoon PhiDivision of Pediatric Neurosurgery, Seoul National University Children's Hospital, Seoul National University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-9603-5843
Seung Ah ChoiDivision of Pediatric Neurosurgery, Seoul National University Children's Hospital, Seoul National University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-4698-6445
Joo Whan KimDivision of Pediatric Neurosurgery, Seoul National University Children's Hospital, Seoul National University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-2286-3301
Chul-Kee ParkDepartment of Neurosurgery, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-2350-9876
Hongseok YunDepartment of Genomic Medicine, Seoul National University Hospital, Seoul, Korea.ORCID https://orcid.org/0000-0003-2776-5954
Young-Soo ParkDepartment of Neurosurgery, Nara Medical University, Nara, Japan.ORCID https://orcid.org/0000-0003-2271-1332
Sung-Hye ParkNeuroscience Research Institute, Seoul National University Medical Research Center, Seoul National University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-8681-1597
Seung-Ki KimDivision of Pediatric Neurosurgery, Seoul National University Children's Hospital, Seoul National University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-0039-0083

Funding

Institute for Information and Communications Technology Promotion 2019-0567Seoul National University Hospital 22A-017-0100Seoul National University Hospital Lee Kun-hee Child Cancer & Rare Disease Project 24C-039-0000
6 · The paper itself

Abstract

backgroundWhile the clinical course of radiation-induced meningioma (RIM) is considered to be more aggressive than that of sporadic meningioma (SM), the genetic predisposition for RIM is not established well. The present study aimed to analyze the clinical and genetic characteristics of RIMs to increase understanding of the tumorigenesis and prognosis of RIMs.

methodsWe investigated a database of 24 patients who met the RIM criteria between January 2000 and April 2023. Genetic analysis through next-generation sequencing with a targeted gene panel was performed on 10 RIM samples. Clinical, radiological, and pathological parameters were evaluated with genetic analyses.

resultsThe median ages for receiving radiotherapy (RT) and RIM diagnosis were 8.0 and 27.5 years, respectively, with an interval of 17.5 years between RT and RIM diagnosis. RIMs tended to develop in non-skull bases and multifocal locations. Most primary pathologies included germ cell tumors and medulloblastoma. The tumor growth rate was 3.83 cm³ per year, and the median doubling time was 0.8 years. All patients underwent surgical resection of RIMs. The histological grade of RIMs was World Health Organization grade 1 (64%) or 2 (36%). RIMs showed higher incidences in young-age (63%), high-dose (75%), and extended-field (79%) RT groups. The recurrence rate was 21%. Genetic analysis revealed

conclusionThe study reveals a higher prevalence of high-grade tumors among RIMs with more rapid growth and higher recurrences than SMs. Genetically, RIMs are primarily associated with

Indexed as

Epigenesis, GeneticHistonesMeningeal NeoplasmsMeningiomaNeoplasms, Radiation-InducedNeurofibromin 2AdolescentAdultChildFemaleHigh-Throughput Nucleotide SequencingHumansMalePrognosisTelomeraseYoung AdultHistonesNeurofibromin 2NF2 protein, humanTelomeraseBrain NeoplasmGenetic TestingH3K27me3MeningiomaPediatricRadiation

Identifiers

PMID40359980
PMCPMC12070044

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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.