Evidence map›Paper›PMID 40851364›Full record

ArticleNeuro-oncology2025

Rapid intraoperative genetic analysis of adult-type diffuse gliomas using a microfluidic real-time polymerase chain reaction device.

Sachi Maeda, Yotaro Kitano, Fumiharu Ohka, Kazuya Motomura, Kosuke Aoki, Shoichi Deguchi, Yoshiki Shiba, Masafumi Seki, Yuma Ikeda, Hiroki Shimizu and 14 more

Abstract read
In one paragraph

Article in Neuro-oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Contemporary surgical strategies for resection of intracranial gliomas.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    Review
  2. Article
  3. 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

24 authors.

Sachi MaedaDepartment of Neurosurgery, Graduate School of Medicine, Nagoya University, Nagoya, Japan.
Yotaro KitanoDepartment of Neurosurgery, Graduate School of Medicine, Mie University, Tsu, Japan.
Fumiharu OhkaDepartment of Neurosurgery, Graduate School of Medicine, Nagoya University, Nagoya, Japan.ORCID 0000-0002-5569-5626
Kazuya MotomuraDepartment of Neurosurgery, Graduate School of Medicine, Nagoya University, Nagoya, Japan.ORCID 0000-0002-4376-1104
Kosuke AokiDepartment of Neurosurgery, Graduate School of Medicine, Nagoya University, Nagoya, Japan.
Shoichi DeguchiDepartment of Neurosurgery, Graduate School of Medicine, Nagoya University, Nagoya, Japan.
Yoshiki ShibaDepartment of Neurosurgery, Graduate School of Medicine, Nagoya University, Nagoya, Japan.
Masafumi SekiDepartment of Pathology and Laboratory Medicine, Graduate School of Medicine, Nagoya University, Nagoya, Japan.
Yuma IkedaDepartment of Pathology and Laboratory Medicine, Graduate School of Medicine, Nagoya University, Nagoya, Japan.
Hiroki ShimizuDepartment of Neurosurgery, Graduate School of Medicine, Nagoya University, Nagoya, Japan.
Kenichiro IwamiDepartment of Neurosurgery, Graduate School of Medicine, Nagoya University, Nagoya, Japan.
Kazuhito TakeuchiDepartment of Neurosurgery, Graduate School of Medicine, Nagoya University, Nagoya, Japan.
Yuichi NagataDepartment of Neurosurgery, Graduate School of Medicine, Nagoya University, Nagoya, Japan.
Junya YamaguchiDepartment of Neurosurgery, Graduate School of Medicine, Nagoya University, Nagoya, Japan.
Keisuke KimuraDepartment of Neurosurgery, Graduate School of Medicine, Nagoya University, Nagoya, Japan.
Yuhei TakidoDepartment of Neurosurgery, Graduate School of Medicine, Nagoya University, Nagoya, Japan.
Ryo YamamotoDepartment of Neurosurgery, Graduate School of Medicine, Nagoya University, Nagoya, Japan.
Akihiro NakamuraDepartment of Neurosurgery, Graduate School of Medicine, Nagoya University, Nagoya, Japan.
Shohei ItoDepartment of Neurosurgery, Graduate School of Medicine, Nagoya University, Nagoya, Japan.
Keiko ShinjoDivision of Cancer Biology, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID 0000-0002-7797-6453
Yutaka KondoDivision of Cancer Biology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Shohei MiyagiDepartment of Pathology and Laboratory Medicine, Graduate School of Medicine, Nagoya University, Nagoya, Japan.
Kennosuke KarubeDepartment of Pathology and Laboratory Medicine, Graduate School of Medicine, Nagoya University, Nagoya, Japan.
Ryuta SaitoDepartment of Neurosurgery, Graduate School of Medicine, Nagoya University, Nagoya, Japan.

Funding

AMED JP23ck0106816
6 · The paper itself

Abstract

backgroundThe 5th edition of the World Health Organization Classification of Tumors of the CNS introduced a subclassification of tumors based on key molecular markers. In adult-type diffuse gliomas, isocitrate dehydrogenase (IDH) and telomerase reverse transcriptase (TERT) promoter mutations play pivotal roles in the molecular classification. This study developed a rapid genotyping system using GeneSoC, a real-time PCR platform with microfluidic thermal cycling capable of completing 50 cycles of PCR within 20 min.

methodsTo establish optimal analytical conditions, frozen tumor tissues from 67 patients and artificial DNA vectors were analyzed using this system. This system demonstrated a detection limit of at least 5% variant allele frequency for the IDH1 R132H and TERT promoter C228T/C250T mutations. Subsequently, intraoperative testing was performed in 120 cases using this system.

resultsThe sensitivity and specificity of IDH1 R132H mutation were 0.985 and 0.982, respectively, whereas those of TERT promoter C228T/C250T mutation were 1.000 and 1.000, respectively. These mutations were detected intraoperatively within approximately 25 min after tumor tissue collection. Furthermore, this assay identified tumor boundaries in an IDH-mutated glioma case, where IDH1 R132H mutations could not be detected.

conclusionsThe GeneSoC®︎-based rapid genotyping system may be effective not only for intraoperative diagnosis of diffuse glioma but also for detecting tumor boundaries.

Indexed as

Biomarkers, TumorBrain NeoplasmsGliomaIsocitrate DehydrogenaseMutationReal-Time Polymerase Chain ReactionTelomeraseAdultAgedFemaleGenotypeHumansMaleMiddle AgedPrognosisPromoter Regions, GeneticBiomarkers, TumorIDH1 protein, humanIsocitrate DehydrogenaseTelomeraseTERT protein, humanadult-type diffuse gliomaIDH mutationintraoperative genotypingTERT promoter mutation

Identifiers

PMID40851364
PMCPMC12965051

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.