Evidence map›Paper›PMID 32246395›Full record

ArticleJournal of neuro-oncology2020

GD2 targeting by dinutuximab beta is a promising immunotherapeutic approach against malignant glioma.

Sascha Marx, Fabian Wilken, Isabel Wagner, Madlen Marx, Sascha Troschke-Meurer, Maxi Zumpe, Sandra Bien-Moeller, Martin Weidemeier, Joerg Baldauf, Steffen K Fleck and 4 more

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of neuro-oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.3field-weighted citation impact, top 11% 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.

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

15 citing papers in PubMed, 24 citations in OpenAlex.

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  7. Targeting Oncogenic Rewiring of Lipid Metabolism for Glioblastoma Treatment.International journal of molecular sciences · 2022
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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

14 authors at 1 institution in 1 country.

Sascha MarxDepartment of Neurosurgery, University Medicine Greifswald, 17475, Greifswald, Germany. sascha.marx@uni-greifswald.de.ORCID http://orcid.org/0000-0002-6451-5404
Fabian WilkenDepartment of Neurosurgery, University Medicine Greifswald, 17475, Greifswald, Germany.
Isabel WagnerDepartment of Neurosurgery, University Medicine Greifswald, 17475, Greifswald, Germany.
Madlen MarxDepartment of Pediatric Oncology and Hematology, University Medicine Greifswald, 17475, Greifswald, Germany.ORCID http://orcid.org/0000-0003-2040-0514
Sascha Troschke-MeurerDepartment of Pediatric Oncology and Hematology, University Medicine Greifswald, 17475, Greifswald, Germany.ORCID http://orcid.org/0000-0002-6185-462X
Maxi ZumpeDepartment of Pediatric Oncology and Hematology, University Medicine Greifswald, 17475, Greifswald, Germany.ORCID http://orcid.org/0000-0003-0297-6739
Sandra Bien-MoellerDepartment of Neurosurgery, University Medicine Greifswald, 17475, Greifswald, Germany.
Martin WeidemeierDepartment of Neurosurgery, University Medicine Greifswald, 17475, Greifswald, Germany.
Joerg BaldaufDepartment of Neurosurgery, University Medicine Greifswald, 17475, Greifswald, Germany.
Steffen K FleckDepartment of Neurosurgery, University Medicine Greifswald, 17475, Greifswald, Germany.
Bernhard H RauchDepartment of Pharmacology, C_DAT, University Medicine Greifswald, 17475, Greifswald, Germany.
Henry W S SchroederDepartment of Neurosurgery, University Medicine Greifswald, 17475, Greifswald, Germany.
Holger LodeDepartment of Pediatric Oncology and Hematology, University Medicine Greifswald, 17475, Greifswald, Germany.ORCID http://orcid.org/0000-0002-1201-208X
Nikolai SiebertDepartment of Pediatric Oncology and Hematology, University Medicine Greifswald, 17475, Greifswald, Germany.ORCID http://orcid.org/0000-0001-6254-1302
Universitätsmedizin Greifswald · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeDisialoganglioside GD

methodsExpression levels of GD2 and complement regulatory proteins (CRP; CD46, CD55 and CD59) on well-known and newly established primary tumor originated GBM cell lines were analyzed by flow cytometry. Ab-dependent cellular (ADCC) and complement-dependent cytotoxicity (CDC) mediated by dinutuximab beta against GBM cells were determined by a non-radioactive calcein-AM-based assay.

resultsAnalysis of primary GBM cells revealed a heterogeneous GD2 expression that varied between the cell lines analyzed with higher expression levels in the tumor surface compared to the core originated cells. Both GD2-positive and -negative tumor cells were detected in every cell line analyzed. In contrast to CDC, ADCC mediated by dinutuximab beta was observed against the majority of GBM cells. Importantly, CDC-resistant cells showed high expression of the CRP CD46, CD55 and CD59.

conclusionOur present data show anti-tumor effects mediated by dinutuximab beta against GBM cells providing a rationale for a GD2-directed immunotherapy against GBM. Due to high CRP expression, a combining of GD2-targeting with CRP blockade might be a further treatment option for GBM.

Indexed as

Antibodies, MonoclonalAntineoplastic AgentsBrain NeoplasmsCell Line, TumorGangliosidesGene Expression Regulation, NeoplasticGliomaHumansImmunotherapyAntibodies, MonoclonalAntineoplastic AgentsdinutuximabGangliosidessialogangliosidesADCCCDCComplement regulating proteinsDinutuximab betaGD2GlioblastomaGliomaImmunotherapy

Identifiers

PMID32246395
OpenAlexW3014642446

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.