Evidence map›Paper›PMID 41120656›Full record

ReviewPaediatric drugs2026

Medulloblastoma: Current Standard of Care and Future Treatment Opportunities.

Lisa Mayr, Amedeo A Azizi, Johannes Gojo, Andreas Peyrl

Abstract readReview
In one paragraph

Review in Paediatric drugs, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. 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

4 authors.

Lisa MayrDepartment of Pediatrics and Adolescent Medicine, Medical University of Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria.
Amedeo A AziziDepartment of Pediatrics and Adolescent Medicine, Medical University of Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria.
Johannes GojoDepartment of Pediatrics and Adolescent Medicine, Medical University of Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria.
Andreas PeyrlDepartment of Pediatrics and Adolescent Medicine, Medical University of Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria. andreas.peyrl@meduniwien.ac.at.ORCID http://orcid.org/0000-0002-5736-8231

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Medulloblastoma, the most common malignant brain tumor of childhood, is an aggressive embryonal tumor that arises from the posterior fossa. On the molecular level, four clinically relevant subgroups have been established, which have already been integrated into routine diagnostic procedures and treatment stratification. The initial step in treating medulloblastoma typically involves maximal safe surgical resection, followed by craniospinal irradiation in most patients (except very young children) and chemotherapy. Efforts to improve cure rates and reduce long-term detrimental effects led to the reduction in radiotherapy and adaptation of chemotherapy. Gradually, over the past decades, these strategies have resulted in significant improvements in treatment outcomes. However, patients with a medulloblastoma recurrence still fare badly, especially those children who already had radiotherapy as part of their initial treatment. Whereas there is no universal treatment strategy at relapse and the outcome remains poor, recently, the administration of anti-angiogenic metronomic therapy led to sustained long-term survival in a quarter of patients. Nonetheless, there remains an unmet need to improve survival and mitigate therapy-induced morbidity by developing new treatment strategies. Promising new approaches include targeting the Sonic Hedgehog pathway, addressing transcriptional and epigenetic drivers, improving drug delivery, and overcoming treatment resistance. Although the most common malignant brain tumor of childhood, the number of novel approaches in addition to a molecularly subdivided entity renders it difficult to form large clinical trials.

Indexed as

Antineoplastic AgentsCerebellar NeoplasmsMedulloblastomaChildHumansStandard of CareAntineoplastic Agents

Identifiers

PMID41120656
PMCPMC12864240

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.