Evidence map›Paper›PMID 40800943›Full record

ArticleImaging neuroscience (Cambridge, Mass.)2025

Detecting glioblastoma infiltration beyond conventional imaging tumour margins using MTE-NODDI.

Saketh R Karamched, Dunja Gorup, Daniele Tolomeo, Lucy J Brooks, Ting Gong, Andreas Christ Sølvsten Jørgensen, Ciaran Scott Hill, Melanie Clements, Tammy L Kalber, Jack A Wells and 7 more

Abstract read
In one paragraph

Article in Imaging neuroscience (Cambridge, Mass.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

1 citing paper in PubMed.

  1. Review
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

17 authors.

Saketh R KaramchedUCL Centre for Advanced Biomedical Imaging, Division of Medicine, University College London, London, United Kingdom.
Dunja GorupUCL Centre for Advanced Biomedical Imaging, Division of Medicine, University College London, London, United Kingdom.
Daniele TolomeoIXICO plc, London, United Kingdom.
Lucy J BrooksSamantha Dickson Brain Cancer Unit, UCL Cancer Institute, London, United Kingdom.
Ting GongUCL Hawkes Institute, Department of Computer Science, University College London, London, United Kingdom.
Andreas Christ Sølvsten JørgensenDepartment of Mathematics, Faculty of Natural Sciences, Imperial College London, London, United Kingdom.
Ciaran Scott HillSamantha Dickson Brain Cancer Unit, UCL Cancer Institute, London, United Kingdom.
Melanie ClementsSamantha Dickson Brain Cancer Unit, UCL Cancer Institute, London, United Kingdom.
Tammy L KalberUCL Centre for Advanced Biomedical Imaging, Division of Medicine, University College London, London, United Kingdom.
Jack A WellsUCL Centre for Advanced Biomedical Imaging, Division of Medicine, University College London, London, United Kingdom.
Daniel J StuckeyUCL Centre for Advanced Biomedical Imaging, Division of Medicine, University College London, London, United Kingdom.
Lewis ThorneDepartment of Neurosurgery, The National Hospital for Neurology and Neurosurgery, London, United Kingdom.
Vahid ShahrezaeiDepartment of Mathematics, Faculty of Natural Sciences, Imperial College London, London, United Kingdom.
Samuel MargueratUCL Cancer Institute, London, United Kingdom.
Hui ZhangUCL Hawkes Institute, Department of Computer Science, University College London, London, United Kingdom.
Simona ParrinelloSamantha Dickson Brain Cancer Unit, UCL Cancer Institute, London, United Kingdom.
Mark F LythgoeUCL Centre for Advanced Biomedical Imaging, Division of Medicine, University College London, London, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma (GBM) is the most common and aggressive brain tumour with starkresistance to available therapies, leading to relapse and a median survival of<15 months. A key cause of therapy resistance is diffuse infiltration oftumour cells into brain regions surrounding the tumour, which presents a majorclinical challenge as existing imaging techniques offer limited detection of theresectable margin. Here, we use diffusion weighted imaging (DWI) and apply themultiple echo time neurite orientation dispersion and density imaging(MTE-NODDI) model as a tool to detect tumour cells in the hard-to-distinguishmargin. We used the G144 patient-derived xenograft model, with characteristicinvasion along white matter tracts, in combination with MTE-NODDI. Tumourdevelopment was monitored, and magnetic resonance imaging (MRI) data wereacquired over a 4-week period, starting at 4 weeks after stereotactic injectionof tumour cells. MTE-NODDI demonstrated sensitivity to the developing tumour inthe invading margin, and changes in measured parameters were apparent from 6weeks after injection. In comparison to standard DWI, MTE-NODDI showed increasedsensitivity to the tumour-associated changes in the margin. Furthermore,extraneurite volume fraction (

Indexed as

diffusion-weighted imagingglioblastomaimaging biomarkersmultiple echo-time NODDINODDItranslational imagingtumour cellstumour invasion

Identifiers

PMID40800943
PMCPMC12319949

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.