Evidence map›Paper›PMID 42240773›Full record

Observational studyJournal of neuro-oncology2026

Report of treatment intensity and survival outcomes in older patients with glioblastoma diagnosed according to WHO CNS 5 classification.

Sophie Therese Williams, Sarah Kingdon, Ola Rominiyi, Cressida Lorimer, Edward Chandy, Mareike Thompson, Ciaran Scott Hill, Giles Critchley, Stephen David Robinson, Histo-Mol GBM collaborative

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Journal of neuro-oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Sophie Therese WilliamsDivision of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UK.ORCID http://orcid.org/0000-0002-5843-0295
Sarah KingdonTessa Jowell Brain Cancer Mission, London, UK.ORCID http://orcid.org/0000-0002-6582-9632
Ola RominiyiDivision of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UK.ORCID http://orcid.org/0000-0002-9724-0224
Cressida LorimerSussex Cancer Centre, University Hospitals Sussex NHS Foundation Trust, Brighton, UK.ORCID http://orcid.org/0000-0001-9299-7394
Edward ChandySussex Cancer Centre, University Hospitals Sussex NHS Foundation Trust, Brighton, UK.ORCID http://orcid.org/0000-0002-6117-8692
Mareike ThompsonCambridge University Hospitals NHS Foundation Trust, Cambridge, UK.ORCID http://orcid.org/0000-0001-7128-8353
Ciaran Scott HillNational Hospital for Neurology and Neurosurgery, Brain Tumour Service (Neuro-Oncology), London, UK.ORCID http://orcid.org/0000-0002-4488-4034
Giles CritchleyDepartment of Neurosurgery, University Hospitals Sussex NHS Foundation Trust, Brighton, UK. giles.critchley@nhs.net.
Stephen David RobinsonSussex Cancer Centre, University Hospitals Sussex NHS Foundation Trust, Brighton, UK. stephen.robinson@nhs.net.ORCID http://orcid.org/0000-0003-0623-4636
Histo-Mol GBM collaborative

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeGlioblastoma is the most common primary brain cancer in adults, with half of cases diagnosed in patients aged ≥ 65 years. However, definitions of older adults vary, resulting in treatment variation between centres. This study aimed to report on the treatment intensity and survival outcomes in older patients with glioblastoma diagnosed according to WHO CNS 5 classification.

methodsWe conducted a retrospective, multicentre cohort study (Histo-Mol GBM Collaborative) of consecutive patients with pathologically confirmed glioblastoma, IDH-wildtype diagnosed in 2021, according to the 2021 WHO CNS 5 classification, across 52 centres in the UK, Ireland, New Zealand, and Australia. Demographic, molecular, treatment, and survival data were analysed.

resultsOf 1,857 patients, 863 (46.5%) were aged ≥ 65 years. Older patients had worse performance status, were more likely to have a biopsy, and received less intensive oncological therapy. Molecular testing was less comprehensive for older patients, but in those patients tested there was no difference with older age. Median overall survival declined with older age, with the steepest reduction in patients ≥ 70 years. Patients aged 65-69 derived comparable benefit from conventionally fractionated chemoradiation to adults aged < 65, whereas outcomes in those aged ≥ 70 were equivalent when treated with hypofractionated or conventionally fractionated chemoradiation. In multivariate analysis, oncological treatment intensity, completion of adjuvant therapy, and MGMT promoter methylation were independent predictors of survival.

conclusionsThis international clinical dataset of adults diagnosed with glioblastoma since the introduction of the WHO CNS 5 criteria supports the use of conventionally fractionated chemoradiation in fit patients < 70, while hypofractionated regimens are appropriate for those ≥ 70. Surgical extent, treatment intensity, and MGMT methylation remain key determinants of survival in older patients with glioblastoma.

Indexed as

Brain NeoplasmsChemoradiotherapyGlioblastomaAgedAged, 80 and overAge FactorsFemaleFollow-Up StudiesHumansMaleMiddle AgedPrognosisRetrospective StudiesSurvival RateCIMPACT-NOWGlioblastomaOlder adultsSurvival outcomesWHO CNS 5

Identifiers

PMID42240773
PMCPMC13236755

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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.