Evidence map›Paper›PMID 40244521›Full record

ArticleJournal of neuro-oncology2025

Combined peritumoral radiomics and clinical features predict 12-month progression free survival in glioblastoma.

Yeong Chul Yun, Johann M E Jende, Freya Garhöfer, Sabine Wolf, Katharina Holz, Anja Hohmann, Philipp Vollmuth, Martin Bendszus, Heinz-Peter Schlemmer, Felix Sahm and 4 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. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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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

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

14 authors.

Yeong Chul YunDepartment of Neuroradiology, Heidelberg University Hospital, Im Neuenheimer Feld 400, Heidelberg, 69120, Germany. YeongChul.Yun@med.uni-heidelberg.de.ORCID http://orcid.org/0009-0005-3552-4968
Johann M E JendeDepartment of Neuroradiology, Heidelberg University Hospital, Im Neuenheimer Feld 400, Heidelberg, 69120, Germany.
Freya GarhöferDepartment of Neuroradiology, Heidelberg University Hospital, Im Neuenheimer Feld 400, Heidelberg, 69120, Germany.
Sabine WolfDepartment of Neuroradiology, Heidelberg University Hospital, Im Neuenheimer Feld 400, Heidelberg, 69120, Germany.
Katharina HolzDepartment of Neuroradiology, Heidelberg University Hospital, Im Neuenheimer Feld 400, Heidelberg, 69120, Germany.
Anja HohmannDepartment of Neurology, Heidelberg University Hospital, Heidelberg, Germany.
Philipp VollmuthDepartment of Neuroradiology, Heidelberg University Hospital, Im Neuenheimer Feld 400, Heidelberg, 69120, Germany.
Martin BendszusDepartment of Neuroradiology, Heidelberg University Hospital, Im Neuenheimer Feld 400, Heidelberg, 69120, Germany.
Heinz-Peter SchlemmerDivision of Radiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Felix SahmDepartment of Neuropathology, Heidelberg University Hospital, Heidelberg, Germany.
Sabine HeilandDepartment of Neuroradiology, Heidelberg University Hospital, Im Neuenheimer Feld 400, Heidelberg, 69120, Germany.
Wolfgang WickDepartment of Neurology, Heidelberg University Hospital, Heidelberg, Germany.
Varun VenkataramaniDepartment of Neurology, Heidelberg University Hospital, Heidelberg, Germany.
Felix T KurzDivision of Radiology, German Cancer Research Center (DKFZ), Heidelberg, Germany. FelixTobias.Kurz@hcuge.ch.ORCID http://orcid.org/0000-0001-7616-7147

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAnalyzing post-treatment MRIs from glioblastoma patients can be challenging due to similar radiological presentations of disease progression and treatment effects. Identifying radiomics features (RFs) revealing progressive glioblastoma can contribute to an improved evaluation of the response assessment.

methods3 Tesla MRI data from 560 glioblastoma patients (mean age 58.1 years) after treatment according to Stupp's protocol were analyzed retrospectively. A total of 418 RFs were extracted from contrast-enhancing tumors, non-enhancing lesions, peritumoral regions (PeriCET) and normal-appearing white matter as regions of interest using PyRadiomics. Dataset was initially split into a training (70%) and a validation (30%) cohort. The training cohort was used for feature selection and model-optimization. Logistic regression was used as a machine-learning model to identify patients with progression-free survival (PFS) as defined by the RANO criteria at 6 and 12 months after treatment. Models were trained with (i) clinical features only, (ii) RFs only, and (iii) a combination of clinical and radiomics features. The performance of each model was evaluated with the validation cohort.

resultsThe predictive performances of the model trained with only RFs from the PeriCET were AUC = 0.61 (95%-CI: 0.51-0.70) and AUC = 0.71 (95%-CI: 0.61-0.81) for 6-months and 12-months PFS respectively. Combining clinical and RFs from PeriCET resulted in overall best performance in predicting patients with progression within 12-months AUC = 0.75 (95%-CI: 0.65-0.85).

conclusionRFs from peritumoral region combined with clinical features including age, sex, and MGMT status can identify patients with 12-months PFS, suggesting the important role of peritumoral regions for the progression of glioblastoma.

Indexed as

Brain NeoplasmsGlioblastomaMagnetic Resonance ImagingAdultAgedDisease ProgressionFemaleFollow-Up StudiesHumansMachine LearningMaleMiddle AgedPrognosisProgression-Free SurvivalRadiomicsRetrospective StudiesGlioblastomaMRIProgression-free survivalRadiomicsRANO

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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.