Evidence map›Paper›PMID 36920679›Full record

ArticleJournal of neuro-oncology2023

Medulloblastoma in adults: evaluation of the Dutch society for neuro-oncology treatment protocol.

L Bleeker, M C M Kouwenhoven, I de Heer, B I Lissenberg-Witte, A H Gijsbers, H J Dubbink, J M Kros, J M M Gijtenbeek, E Kurt, C C D van der Rijt and 7 more

Open access · hybridFull text read
In one paragraph

Article in Journal of neuro-oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Brain Tumor Classification by Methylation Profile.Journal of Korean medical science · 2023
    Review
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 at 7 institutions in 1 country.

L BleekerBrain Tumor Center Amsterdam, Department of Neurology, Amsterdam UMC, Amsterdam, The Netherlands. l.bleeker@olvg.nl.ORCID http://orcid.org/0000-0003-1338-1167
M C M KouwenhovenBrain Tumor Center Amsterdam, Department of Neurology, Amsterdam UMC, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0001-5252-4365
I de HeerBrain Tumor Center, Department of Neurology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0003-3178-7603
B I Lissenberg-WitteDepartment of Epidemiology and Data Science, Amsterdam UMC, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0001-9448-1826
A H GijsbersThe Nationwide Network and Registry of Histopathology and Cytopathology in the Netherlands (PALGA), Houten, The Netherlands.
H J DubbinkBrain Tumor Center, Department of Pathology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0002-2160-5207
J M KrosBrain Tumor Center, Department of Pathology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0002-4727-0724
J M M GijtenbeekDepartment of Neurology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.ORCID http://orcid.org/0000-0002-0844-7259
E KurtDepartment of Neurosurgery, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.ORCID http://orcid.org/0000-0003-3768-4007
C C D van der RijtDepartment of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0001-5996-1242
A T Swaak-KragtenDepartment of Radiation Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0003-4721-5802
F Y de VosCancer Center, Department of Medical Oncology, University Medical Center Utrecht, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0002-9082-5991
H L van der WeideUniversity Medical Center Groningen, Department of Radiation Oncology, University of Groningen, Groningen, The Netherlands.ORCID http://orcid.org/0000-0001-6734-2345
P J FrenchBrain Tumor Center, Department of Neurology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0002-0668-9529
M J van den BentBrain Tumor Center, Department of Neurology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0001-5710-5127
P WesselingDepartment of Pathology, Amsterdam University Medical Centers/VUmc, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0001-5453-5201
J E C BrombergBrain Tumor Center, Department of Neurology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0002-3830-7142
Erasmus MC Cancer Institute · NLAmsterdam Neuroscience · NLRadboud University Nijmegen · NLAmsterdam University Medical Centers · NLPrincess Máxima Center · NLUniversity Medical Center Groningen · NLUniversity Medical Center Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeMedulloblastoma is a rare tumor in adults. The objective of this nationwide, multicenter study was to evaluate the toxicity and efficacy of the Dutch treatment protocol for adult medulloblastoma patients.

methodsAdult medulloblastoma patients diagnosed between 2010 and 2018 were identified in the Dutch rare tumors registry or nationwide pathology database. Patients with intention to treat according to the national treatment protocol were included. Risk stratification was performed based on residual disease, histological subtype and extent of disease. All patients received postoperative radiotherapy [craniospinal axis 36 Gy/fossa posterior boost 19.8 Gy (14.4 Gy in case of metastases)]. High-risk patients received additional neoadjuvant (carboplatin-etoposide), concomitant (vincristine) and adjuvant chemotherapy (carboplatin-vincristine-cyclophosphamide) as far as feasible by toxicity. Methylation profiling, and additional next-generation sequencing in case of SHH-activated medulloblastomas, were performed.

resultsForty-seven medulloblastoma patients were identified, of whom 32 were treated according to the protocol. Clinical information and tumor material was available for 28 and 20 patients, respectively. The histological variants were mainly classic (43%) and desmoplastic medulloblastoma (36%). Sixteen patients (57%) were considered standard-risk and 60% were SHH-activated medulloblastomas. Considerable treatment reductions and delays in treatment occurred due to especially hematological and neurotoxicity. Only one high-risk patient could complete all chemotherapy courses. 5-years progression-free survival (PFS) and overall survival (OS) for standard-risk patients appeared worse than for high-risk patients (PFS 69% vs. 90%, OS 81% vs. 90% respectively), although this wasn't statistically significant.

conclusionCombined chemo-radiotherapy is a toxic regimen for adult medulloblastoma patients that may result in improved survival.

Indexed as

Cerebellar NeoplasmsMedulloblastomaAdultAntineoplastic Combined Chemotherapy ProtocolsCarboplatinCombined Modality TherapyHumansMulticenter Studies as TopicVincristineCarboplatinVincristineAdultsMedulloblastomaMethylation arrayToxicityTreatment

Identifiers

PMID36920679
PMCPMC10050065
OpenAlexW4324306012

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read112
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.