Evidence map›Paper›PMID 36333718›Full record

ArticleBMC medical genomics2022

Study protocol of the GLOW study: maximising treatment options for recurrent glioblastoma patients by whole genome sequencing-based diagnostics-a prospective multicenter cohort study.

Mark P van Opijnen, Marike L D Broekman, Filip Y F de Vos, Edwin Cuppen, Jacobus J M van der Hoeven, Myra E van Linde, Annette Compter, Laurens V Beerepoot, Martin J van den Bent, Maaike J Vos and 8 more

Registry-linked trialOpen access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in BMC medical genomics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05186064 (Glioblastoma Targeted Treatment Option Maximization by Whole Genome Sequencing), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 24% of its field
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.

NCT05186064 nacompletednot on this map

Glioblastoma Targeted Treatment Option Maximization by Whole Genome Sequencing

TypeinterventionalSponsorUMC UtrechtRan2022 to 2025Enrolled164ConditionsGlioblastomaArmswhole genome sequencing
3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 7 citations in OpenAlex.

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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

18 authors at 14 institutions in 1 country.

Mark P van OpijnenDepartment of Neurosurgery, Haaglanden Medical Center, The Hague, The Netherlands.
Marike L D BroekmanDepartment of Neurosurgery, Haaglanden Medical Center, The Hague, The Netherlands.
Filip Y F de VosDepartment of Medical Oncology, Utrecht University Medical Center, Utrecht, The Netherlands. f.devos@umcutrecht.nl.ORCID 0000-0002-9082-5991
Edwin CuppenHartwig Medical Foundation, Amsterdam, The Netherlands.
Jacobus J M van der HoevenHartwig Medical Foundation, Amsterdam, The Netherlands.
Myra E van LindeDepartment of Medical Oncology, Amsterdam University Medical Centers, Amsterdam, The Netherlands.
Annette CompterDepartment of Neurology, Netherlands Cancer Institute-Antoni Van Leeuwenhoek, Amsterdam, The Netherlands.
Laurens V BeerepootDepartment of Medical Oncology, Elisabeth-Tweesteden Hospital, Tilburg, The Netherlands.
Martin J van den BentDepartment of Neurology, Erasmus Medical Center, Rotterdam, The Netherlands.
Maaike J VosDepartment of Neurology, Haaglanden Medical Center, The Hague, The Netherlands.
Helle-Brit FiebrichDepartment of Medical Oncology, Isala Clinics, Zwolle, The Netherlands.
Johan A F KoekkoekDepartment of Neurology, Haaglanden Medical Center, The Hague, The Netherlands.
Ann HoebenDepartment of Medical Oncology, University Hospital Maastricht, Maastricht, The Netherlands.
Kuan H KhoDepartment of Neurosurgery, Neurocenter, Medisch Spectrum Twente, Enschede, The Netherlands.
Chantal M L DriessenDepartment of Medical Oncology, Radboud University Medical Center, Nijmegen, The Netherlands.
Hanne-Rinck JeltemaDepartment of Neurosurgery, University Medical Center Groningen, Groningen, The Netherlands.
Pierre A J T RobeDepartment of Neurology and Neurosurgery, University Medical Center Utrecht, Utrecht, The Netherlands.
Sybren L N MaasDepartment of Pathology, Leiden University Medical Center, Leiden, The Netherlands.
Leiden University Medical Center · NLUniversity Medical Center Utrecht · NLAmsterdam University Medical Centers · NLElisabeth-TweeSteden Ziekenhuis · NLErasmus MC · NLHartwig Medical Foundation · NLIsala · NLMaastricht University Medical Centre · NLMedisch Centrum Haaglanden · NLMedisch Spectrum Twente · NLRadboud University Nijmegen · NLThe Netherlands Cancer Institute · NLUniversity Medical Center Groningen · NLUtrecht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGlioblastoma (GBM), the most common glial primary brain tumour, is without exception lethal. Every year approximately 600 patients are diagnosed with this heterogeneous disease in The Netherlands. Despite neurosurgery, chemo -and radiation therapy, these tumours inevitably recur. Currently, there is no gold standard at time of recurrence and treatment options are limited. Unfortunately, the results of dedicated trials with new drugs have been very disappointing. The goal of the project is to obtain the evidence for changing standard of care (SOC) procedures to include whole genome sequencing (WGS) and consequently adapt care guidelines for this specific patient group with very poor prognosis by offering optimal and timely benefit from novel therapies, even in the absence of traditional registration trials for this small volume cancer indication.

methodsThe GLOW study is a prospective diagnostic cohort study executed through collaboration of the Hartwig Medical Foundation (Hartwig, a non-profit organisation) and twelve Dutch centers that perform neurosurgery and/or treat GBM patients. A total of 200 patients with a first recurrence of a glioblastoma will be included. Dual primary endpoint is the percentage of patients who receive targeted therapy based on the WGS report and overall survival. Secondary endpoints include WGS report success rate and number of targeted treatments available based on WGS reports and number of patients starting a treatment in presence of an actionable variant. At recurrence, study participants will undergo SOC neurosurgical resection. Tumour material will then, together with a blood sample, be sent to Hartwig where it will be analysed by WGS. A diagnostic report with therapy guidance, including potential matching off-label drugs and available clinical trials will then be sent back to the treating physician for discussing of the results in molecular tumour boards and targeted treatment decision making. DISCUSSION: The GLOW study aims to provide the scientific evidence for changing the SOC diagnostics for patients with a recurrent glioblastoma by investigating complete genome diagnostics to maximize treatment options for this patient group.

trial registrationClinicalTrials.gov Identifier: NCT05186064.

Indexed as

Brain NeoplasmsGlioblastomaChronic DiseaseHumansMulticenter Studies as TopicNeoplasm Recurrence, LocalProspective StudiesWhole Genome SequencingDiagnosticsGlioblastomaRecurrenceTreatment optionsWhole genome sequencing

Identifiers

PMID36333718
PMCPMC9636658
OpenAlexW4308354355

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Registered trials

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.