Evidence map›Paper›PMID 38503417›Full record

ArticleBMJ open2024

Adjuvant Wilms' tumour 1-specific dendritic cell immunotherapy complementing conventional therapy for paediatric patients with high-grade glioma and diffuse intrinsic pontine glioma: protocol of a monocentric phase I/II clinical trial in Belgium.

Toon Van Genechten, Maxime De Laere, Jolien Van den Bossche, Barbara Stein, Kim De Rycke, Caroline Deschepper, Katja Hazes, Renke Peeters, Marie-Madeleine Couttenye, Katrien Van De Walle and 14 more

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

Article in BMJ open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04911621 (Adjuvant Dendritic Cell Immunotherapy Complementing Conventional Therapy for Pediatric Patients With High-grade Glioma and Diffuse Intrinsic Pontine Glioma), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 32% 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.

NCT04911621 phase1 / phase2completednot on this map

Adjuvant Dendritic Cell Immunotherapy Complementing Conventional Therapy for Pediatric Patients With High-grade Glioma and Diffuse Intrinsic Pontine Glioma

TypeinterventionalSponsorUniversity Hospital, AntwerpRan2021 to 2025Enrolled10ConditionsHigh Grade Glioma, Diffuse Intrinsic Pontine GliomaArmsDendritic cell vaccination + temozolomide-based chemoradiation, Dendritic cell vaccination +- conventional next-line treatment
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 3 citations in OpenAlex.

  1. Advances inMolecular therapy. Nucleic acids · 2026
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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

24 authors at 2 institutions in 1 country.

Toon Van GenechtenPediatric Oncology, University Hospital Antwerp, Edegem, Antwerpen, Belgium toon.vangenechten@uza.be.ORCID 0000-0002-3787-9667
Maxime De LaereLaboratory of Experimental Hematology, Vaccine & Infectious Disease Institute, University of Antwerp Faculty of Medicine and Health Sciences, Wilrijk, Belgium.
Jolien Van den BosscheLaboratory of Experimental Hematology, Vaccine & Infectious Disease Institute, University of Antwerp Faculty of Medicine and Health Sciences, Wilrijk, Belgium.
Barbara SteinCenter for Cell Therapy and Regenerative Medicine, University Hospital Antwerp, Edegem, Antwerpen, Belgium.
Kim De RyckeCenter for Cell Therapy and Regenerative Medicine, University Hospital Antwerp, Edegem, Antwerpen, Belgium.
Caroline DeschepperPediatric Oncology, University Hospital Antwerp, Edegem, Antwerpen, Belgium.
Katja HazesPediatric Oncology, University Hospital Antwerp, Edegem, Antwerpen, Belgium.
Renke PeetersPediatric Oncology, University Hospital Antwerp, Edegem, Antwerpen, Belgium.
Marie-Madeleine CouttenyeDepartment of Nephrology, University Hospital Antwerp, Edegem, Belgium.
Katrien Van De WalleDepartment of Nephrology, University Hospital Antwerp, Edegem, Belgium.
Ella RoelantStatistics, Universitair Ziekenhuis Antwerpen, Edegem, Antwerpen, Belgium.
Sabine MaesAnesthesiology, University Hospital Antwerp, Edegem, Antwerpen, Belgium.
Stephanie Vanden BosscheRadiology, University Hospital Antwerp, Edegem, Antwerpen, Belgium.
Sven DekeyzerRadiology, University Hospital Antwerp, Edegem, Antwerpen, Belgium.
Manon HuizingCell and Tissue Bank, University Hospital Antwerp, Edegem, Antwerp, Belgium.
Kim CaluwaertCenter for Cell Therapy and Regenerative Medicine, University Hospital Antwerp, Edegem, Antwerpen, Belgium.
Griet NijsCenter for Cell Therapy and Regenerative Medicine, University Hospital Antwerp, Edegem, Antwerpen, Belgium.
Nathalie CoolsLaboratory of Experimental Hematology, Vaccine & Infectious Disease Institute, University of Antwerp Faculty of Medicine and Health Sciences, Wilrijk, Belgium.
Joris VerlooyPediatric Oncology, University Hospital Antwerp, Edegem, Antwerpen, Belgium.
Koen NorgaPediatric Oncology, University Hospital Antwerp, Edegem, Antwerpen, Belgium.
Stijn VerhulstPediatrics, University Hospital Antwerp, Edegem, Antwerpen, Belgium.
Sebastien AnguilleLaboratory of Experimental Hematology, Vaccine & Infectious Disease Institute, University of Antwerp Faculty of Medicine and Health Sciences, Wilrijk, Belgium.
Zwi BernemanLaboratory of Experimental Hematology, Vaccine & Infectious Disease Institute, University of Antwerp Faculty of Medicine and Health Sciences, Wilrijk, Belgium.
Eva LionCenter for Cell Therapy and Regenerative Medicine, University Hospital Antwerp, Edegem, Antwerpen, Belgium.
Antwerp University Hospital · BEUniversity of Antwerp · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionDiffuse intrinsic pontine glioma (DIPG) and paediatric high-grade glioma (pHGG) are aggressive glial tumours, for which conventional treatment modalities fall short. Dendritic cell (DC)-based immunotherapy is being investigated as a promising and safe adjuvant therapy. The Wilms' tumour protein (WT1) is a potent target for this type of antigen-specific immunotherapy and is overexpressed in DIPG and pHGG. Based on this, we designed a non-randomised phase I/II trial, assessing the feasibility and safety of METHODS AND ANALYSIS: 10 paediatric patients with newly diagnosed or pretreated HGG or DIPG were treated according to the trial protocol. The trial protocol consists of leukapheresis of mononuclear cells, the manufacturing of autologous WT1/DC vaccines and the combination of WT1/DC-vaccine immunotherapy with conventional antiglioma treatment. In newly diagnosed patients, this comprises chemoradiation (oral temozolomide 90 mg/m ETHICS AND DISSEMINATION: The ethics committee of the Antwerp University Hospital and the University of Antwerp granted ethics approval. Results of the clinical trial will be shared through publication in a peer-reviewed journal and presentations at conferences. TRIAL REGISTRATION NUMBER: NCT04911621.

Indexed as

Cancer VaccinesDiffuse Intrinsic Pontine GliomaGliomaKidney NeoplasmsVaccinesWilms TumorBelgiumChildClinical Trials, Phase I as TopicClinical Trials, Phase II as TopicDendritic CellsHumansImmunotherapyQuality of LifeRNA, MessengerTemozolomideCancer VaccinesRNA, MessengerTemozolomideVaccinesWT1 ProteinsIMMUNOLOGYNeurological oncologyPaediatric oncology

Identifiers

PMID38503417
PMCPMC10952861
OpenAlexW4394738393

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.