Evidence map›Paper›PMID 41247617›Full record

Observational studyJournal of neuro-oncology2025

GLIMMER: an interim subgroup analysis from an ongoing prospective study evaluating hyperspectral imaging for MGMT promoter methylation in gliomas.

Johannes Wach, Ferdinand Weber, Tim Wende, Martin Vychopen, Alonso Barrantes-Freer, Annekatrin Pfahl, Hannes Köhler, Erdem Güresir

Abstract readObservational Study
In one paragraph

Observational study in Journal of neuro-oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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

8 authors.

Johannes Wach *Department of Neurosurgery, University Hospital Leipzig, Leipzig, Saxony, Germany. johannes.wach@medizin.uni-leipzig.de.
Ferdinand Weber *Department of Neurosurgery, University Hospital Leipzig, Leipzig, Saxony, Germany.
Tim WendeDepartment of Neurosurgery, University Hospital Leipzig, Leipzig, Saxony, Germany.
Martin VychopenDepartment of Neurosurgery, University Hospital Leipzig, Leipzig, Saxony, Germany.
Alonso Barrantes-FreerPaul-Flechsig-Institute of Neuropathology, University Hospital Leipzig, Leipzig, Saxony, Germany.
Annekatrin PfahlInnovation Center Computer Assisted Surgery, Faculty of Medicine, Leipzig University, 04103, Leipzig, Saxony, Germany.
Hannes KöhlerInnovation Center Computer Assisted Surgery, Faculty of Medicine, Leipzig University, 04103, Leipzig, Saxony, Germany.
Erdem GüresirDepartment of Neurosurgery, University Hospital Leipzig, Leipzig, Saxony, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMGMT promoter methylation is of importance in glioma regarding prognosis and management. Non-methylated MGMT glioblastoma patients seem to benefit more from gross total resection. MGMT status is not ultra-rapidly available in the operating room. The presents study is the first aiming to evaluate whether the novel imaging technique intraoperative hyperspectral imaging (HSI) can predict MGMT promoter methylation status in glioma patients using a novel optical scoring system.

methodsThis was a prospective subgroup analysis of 25 glioma patients enrolled in a single-center observational study. Patients underwent in-vivo HSI (spectral range: 500-1000 nm) targeting non-contrast-enhancing tumor regions during resection. Two optical parameters-tissue water index (TWI) and organ hemoglobin index (OHI)-were extracted and combined into a novel three-point GLIMMER score. Primary endpoint was MGMT promoter methylation status determined by pyrosequencing. Diagnostic performance of the GLIMMER score was measured by AUC, sensitivity, and specificity. A subgroup analysis focused on IDH-wild-type glioblastoma (n = 16).

resultsOHI ≤ 0.606 and TWI ≥ 0.501 were significantly associated with MGMT promoter methylation. The combined GLIMMER score achieved an AUC of 0.95 (95% CI, 0.87-1.00) with 94.7% sensitivity and 83.3% specificity. In the glioblastoma subgroup, the AUC was 0.97, with 100% sensitivity and 75% specificity. Patients scoring ≥ 1 point had significantly higher MGMT methylation (31.5%) than those scoring 0 points (7.9%; p < 0.001).

conclusionsThe GLIMMER score suggests potential ultra-rapid, non-invasive intraoperative estimation of MGMT promoter methylation with high diagnostic performance. These findings necessitate further validation with in-vivo HSI-guided biopsies to guide future personalized resection strategies in glioma patients. CLINICAL TRIAL NUMBER: German Clinical Trials Register (DRKS, Trial number: DRKS00036771, Registration date: 05.05.2025).

Indexed as

Brain NeoplasmsDNA MethylationDNA Modification MethylasesDNA Repair EnzymesGliomaPromoter Regions, GeneticTumor Suppressor ProteinsAdultAgedFemaleHumansMaleMiddle AgedProspective StudiesDNA Modification MethylasesDNA Repair EnzymesMGMT protein, humanTumor Suppressor ProteinsGlioblastomaGlioma surgeryHyperspectral imagingIntraoperative imagingMGMT promoter methylationOptical biomarkersSupramaximal resection

Identifiers

PMID41247617
PMCPMC12628469

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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.