Evidence map›Paper›PMID 42493681›Full record

ArticleJournal of neuro-oncology2026

Salvage therapies for recurrent grade 4 IDH-wildtype glioma: a BRAIN Registry analysis of real-world treatment patterns.

Emma Sanderson, Katharine Drummond, Anthony Dowling, Iwan Bennett, Ronnie Freilich, Claire Phillips, Elizabeth Ahern, David Campbell, Robert Campbell, Rosemary Harrup and 12 more

Abstract read
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In one paragraph

Article 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

22 authors.

Emma SandersonPersonalised Oncology Division, The Walter and Eliza Hall Institute of Medial Research, Parkville, VIC, Australia. sanderson.e@wehi.edu.au.
Katharine DrummondDepartment of Neurosurgery, Royal Melbourne Hospital, Parkville, VIC, Australia.
Anthony DowlingDepartment of Medical Oncology, St Vincent's Hospital Melbourne, Fitzroy, VIC, Australia.
Iwan BennettDepartment of Neurosurgery, The Alfred, Melbourne, VIC, Australia.
Ronnie FreilichCabrini Hospital, Malvern, VIC, Australia.
Claire PhillipsDepartment of Radiation Oncology, Peter MacCallum Cancer Centre, Parkville, VIC, Australia.
Elizabeth AhernDepartment of Medical Oncology, Monash Health, Clayton, VIC, Australia.
David CampbellDepartment of Medical Oncology, University Hospital Geelong, Barwon Health, Geelong, VIC, Australia.
Robert CampbellDepartment of Medical Oncology, Bendigo Health, Bendigo, VIC, Australia.
Rosemary HarrupCancer & Blood Services, Royal Hobart Hospital, Hobart, TAS, Australia.
Simone ReevesBallarat Austin Radiation Oncology Centre, Ballarat, VIC, Australia.
Ian CollinsDepartment of Medical Oncology, Southwest Healthcare, Warrnambool, VIC, Australia.
Ross JennensEpworth Richmond, Richmond, VIC, Australia.
Sachin JoshiDepartment of Medical Oncology, Latrobe Regional Health, Traralgon, VIC, Australia.
Hui GanDepartment of Medical Oncology, Austin Health, Heidelberg, VIC, Australia.
Michael FayGenesisCare, Newcastle, NSW, Australia.
James LynamCalvary Mater Newcastle and Newcastle Private Hospital, Newcastle, NSW, Australia.
Lisi Elizabeth LimDepartment of Medical Oncology, Grampians Health Ballarat, Ballarat, VIC, Australia.
Mark RosenthalDepartment of Medical Oncology, Peter MacCallum Cancer Centre, Parkville, VIC, Australia.
Megan DumasPersonalised Oncology Division, The Walter and Eliza Hall Institute of Medial Research, Parkville, VIC, Australia.
Peter GibbsPersonalised Oncology Division, The Walter and Eliza Hall Institute of Medial Research, Parkville, VIC, Australia.
Lucy GatelyPersonalised Oncology Division, The Walter and Eliza Hall Institute of Medial Research, Parkville, VIC, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe prognosis for patients with glioblastoma after failure of first-line therapy is poor. Despite this, the standard of care for patients with recurrent disease is not well-defined. Here we report on the use of salvage therapies in glioblastoma using real-world data.

methodsData were extracted from the BRAIN Registry for patients diagnosed with glioblastoma (Grade 4, IDH wild-type) between 09/2019 and 01/2024. Only patients who received salvage therapies following a documented date of recurrence/progression were included. Relevant descriptive and intergroup statistics were used, with survival calculated using Kaplan-Meier and Cox regression used for multivariate analyses.

results275 patients were identified. Median age was 61 (range:23-88) years, with 56% being ECOG 0-1 at recurrence. Median time to progression was 7.6 months with 65% recurring/progressing during first-line therapy. Systemic therapy (85%) was most utilised with 67% receiving single-agent bevacizumab. Outcomes in this subgroup were similar to clinical trial data. 29% patients underwent re-resection with 58% of these then receiving systemic treatment. Compared with no surgery, patients who underwent re-resection were younger (p = 0.02), of better performance status (p = 0.006) and more likely to have recurred post completing first-line therapy (p = 0.001). Few patients (n = 9) received re-irradiation with median of 15 months between radiation events. Median post-progression survival (PPS) was 9.5 months. After adjustment for confounders, there was no difference in PPS for patients who underwent re-resection versus systemic therapy alone (p = 0.242). The survival differences observed between treatment modalities likely reflect patient factors influencing treatment selection and were impacted by small subgroup sizes.

conclusionSystemic therapy is most utilised in the salvage setting, predominantly bevacizumab. Certain patient characteristics were associated with re-resection. Re-irradiation was rarely used. CLINICAL TRIAL NUMBER: ACTRN12618001959268.

Indexed as

Brain NeoplasmsGliomaNeoplasm Recurrence, LocalSalvage TherapyAdultAgedAged, 80 and overBevacizumabFemaleFollow-Up StudiesHumansIsocitrate DehydrogenaseMaleMiddle AgedPrognosisRegistriesBevacizumabIDH1 protein, humanIsocitrate DehydrogenaseGlioblastomaRadiotherapyRecurrenceSurgerySystemic therapyTreatment patterns

Identifiers

What OpenQuestion holds

Textmetadata
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.