Evidence map›Paper›PMID 42428515›Full record

ArticleNeuro-oncology advances

Neurosurgeons' perspective on surgical treatment of glioblastoma: Practices, beliefs and willingness to randomize in surgical trials.

Johnny Duerinck, Louise Lescrauwaet, Philipp Karschnia, Rebeca Pérez Alfayate, Michael D Jenkinson, Eric Suero Molina, Matthias Simon, Jasper Gerritsen, Jorn Van Der Veken, Thiebaud Picart and 7 more

Abstract read
In one paragraph

Article in Neuro-oncology advances. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

17 authors.

Johnny DuerinckDepartment of Neurosurgery, Universitair Ziekenhuis Brussel (UZ Brussel), Brussels, Belgium.ORCID https://orcid.org/0000-0001-9869-9806
Louise LescrauwaetDepartment of Neurosurgery, Universitair Ziekenhuis Brussel (UZ Brussel), Brussels, Belgium.
Philipp KarschniaDepartment of Neurosurgery, Universitaetsklinikum Erlangen-Nuremberg, Friedrich-Alexander-University Erlangen, Erlangen, Germany.ORCID https://orcid.org/0000-0002-1254-5310
Rebeca Pérez AlfayateHospital Clínico San Carlos, Madrid, Spain.
Michael D JenkinsonUniversity of Liverpool, Liverpool, UK.
Eric Suero MolinaDepartment of Neurosurgery, University Hospital Münster, Münster, Germany.
Matthias SimonBethel Clinic, University of Bielefeld Medical Center, Bielefeld, Germany.ORCID https://orcid.org/0000-0001-7508-3072
Jasper GerritsenNeurosurgery, Erasmus Medical Center, Rotterdam, Netherlands.
Jorn Van Der VekenFlinders Medical Centre, Bedford Park, Australia.ORCID https://orcid.org/0000-0002-8351-1978
Thiebaud PicartNeurosurgery, Hôpital Neurologique Pierre Wertheimer, Lyon, France.
Emilie Le RhunDepartment of Medical Oncology and Oncology, Brain Tumor Center, University Hospital and University of Zurich, Zurich, Switzerland.ORCID https://orcid.org/0000-0002-9408-3278
Giuseppe MinnitiDepartment of Radiological Sciences, Oncology and Anatomical Pathology, Sapienza University of Rome, Rome, Italy.
Matthias PreusserDivision of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Michael WellerDepartment of Neurology, University Hospital & University of Zurich, Zurich, Switzerland.ORCID https://orcid.org/0000-0002-1748-174X
Mandy Melissa Jane WittensIMEC-SMIT, Vrije Universiteit Brussel (VUB), Brussels, Belgium.
Asgeir S JakolaSahlgrenska University Hospital, Gothenburg, Sweden, and section of clinical neuroscience, institute of neuroscience and physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg.
Alireza MansouriNeurosurgery, Penn State Health, Hershey, Pennsylvania, USA.ORCID https://orcid.org/0000-0002-7442-7539

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The optimal extent of resection for glioblastoma remains debated, with high-level evidence from randomized controlled trials (RCTs) notably scarce. We aimed to evaluate international surgical practices, perceived quality of evidence, and feasibility of future RCTs through an international survey of neurosurgeons. Methods: An international survey was distributed via European Organization for Research and Treatment of Cancer (EORTC), European Association of Neurosurgical Societies (EANS), Congress of Neurological Surgeons (CNS), and national societies. We used descriptive statistics to summarize surgical practices and univariate analysis and multivariate regression to identify demographic or institutional factors associated with clinical decision-making. Results: Responses were received from 328 neurosurgeons across 38 countries. Participation was predominantly from Europe (81.1%), with 12.2% from North America. Most participants (82.9%) practiced in academic centers. While 60.4% identified supramarginal resection (SMR) as the optimal surgical goal, 37.8% aim for complete resection of enhancing tumor (CRET). Overall, 90.2% viewed the evidence for CRET as strong, compared to 63.1% for SMR. Despite these views, 72.6% expressed willingness to randomize patients between CRET and SMR, while 49.4% would be willing to randomize between partial resection and biopsy, if CRET is not feasible. Despite differences in individual practice, willingness to participate in RCTs remained consistent across geographic regions. The incomplete overlap between case-based decisions and general willingness to randomize highlights the importance of case-specific nuances. A paradox was observed where perceived weak evidence correlated with lower willingness to randomize( Conclusion: There is substantial global willingness among neurosurgeons to participate in surgical RCTs for glioblastoma. These findings provide a foundation for designing future international trials to resolve long-standing controversies regarding optimal surgical strategy for glioblastoma.

Indexed as

clinical equipoiseextent of resection (EOR)glioblastomasupramarginal resectionsurgical randomized controlled trials (RCTs)

Identifiers

PMID42428515
PMCPMC13348702

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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.