Evidence map›Paper›PMID 41530365›Full record

SynthesisActa neurochirurgica2026

Determinants of survival after re-resection for recurrent glioblastoma: a meta-analysis.

Manuel V Baby, Rithvik M Narendranath, Symriti Kaur-Paneser, Daniele S C Ramsay, Hariharan Subbiah Ponniah, Srikar R Namireddy, Ahmed Salih, Ahkash Thavarajasingam, Daniel Scurtu, Andreas Kramer and 5 more

Abstract readMeta-Analysis
In one paragraph

Synthesis in Acta neurochirurgica, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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

15 authors.

Manuel V BabyImperial Brain and Spine Initiative, Imperial College London, London, UK.
Rithvik M NarendranathImperial Brain and Spine Initiative, Imperial College London, London, UK.
Symriti Kaur-PaneserImperial Brain and Spine Initiative, Imperial College London, London, UK.
Daniele S C RamsayImperial Brain and Spine Initiative, Imperial College London, London, UK.
Hariharan Subbiah PonniahImperial Brain and Spine Initiative, Imperial College London, London, UK.
Srikar R NamireddyImperial Brain and Spine Initiative, Imperial College London, London, UK.
Ahmed SalihImperial Brain and Spine Initiative, Imperial College London, London, UK.
Ahkash ThavarajasingamImperial Brain and Spine Initiative, Imperial College London, London, UK.
Daniel ScurtuDepartment of Neurosurgery, University Medical Center Mainz, Mainz, Germany.
Andreas KramerDepartment of Neurosurgery, LMU University Hospital, LMU Munich, Munich, Germany.
Veit StöckleinDepartment of Neurosurgery, LMU University Hospital, LMU Munich, Munich, Germany.
Darius KalasauskasDepartment of Neurosurgery, LMU University Hospital, LMU Munich, Munich, Germany.
Dragan JankovicDepartment of Neurosurgery, LMU University Hospital, LMU Munich, Munich, Germany.
Florian RingelDepartment of Neurosurgery, LMU University Hospital, LMU Munich, Munich, Germany.
Santhosh G ThavarajasingamImperial Brain and Spine Initiative, Imperial College London, London, UK. santhoshgthava@outlook.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeGlioblastoma (GBM) inevitably recurs despite maximal safe resection and standard chemoradiotherapy. The factors influencing survival after first recurrence and re-resection remain controversial. RESEARCH QUESTION: What are the prognostic factors influencing survival following re-resection of glioblastoma?

methodsA systematic search of major databases was conducted for original studies reporting on survival outcomes. Data on hazard ratios (HR) for overall survival and key prognostic factors were extracted, followed by meta-analyses of univariate and multivariate Cox models. Study quality and risk of bias were assessed.

resultsA total of 30 studies were included. Gross total resection and methylated MGMT promoter status were significantly associated with improved survival, with pooled HRs of 0.52 (95% CI: 0.36-0.76, p < 0.001) and 0.58 (95% CI: 0.45-0.75, p < 0.001), respectively. In contrast, age was modestly associated with worse survival (HR: 1.02, 95% CI: 1.01-1.03, p < 0.001). Preoperative Karnofsky Performance Status (KPS) < 70 was associated with worse survival (HR: 2.25, 95% CI: 1.59-3.19, p < 0.001). Adjuvant chemotherapy (HR: 0.69, 95% CI: 0.33-1.45, p = 0.33) and time to re-resection (HR: 0.69, 95% CI: 0.41-1.16, p = 0.16) failed to show consistent survival benefits.

conclusionOur findings suggest gross total resection of contrast-enhancing tumour and MGMT promoter methylation are strongly associated with improved survival following first recurrence of glioblastoma. Conversely, age, preoperative KPS, adjuvant chemotherapy, and timing of re-resection showed inconsistent or non-significant associations, emphasizing the need for prospective studies to refine prognostic assessments and guide individualized treatment strategies in recurrent glioblastoma.

Indexed as

Brain NeoplasmsGlioblastomaNeoplasm Recurrence, LocalHumansPrognosisReoperationGlioblastomaPrognosticRecurrenceRe-resectionSurvival

Identifiers

PMID41530365
PMCPMC12804209

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.