Evidence map›Paper›PMID 42199604›Full record

ReviewMolecular therapy. Oncology2026

New developments and prospects for drug delivery in medulloblastoma.

Kaoutar Bentayebi, Sara Louati, Keittisak Suwan, Rachid Eljaoudi, Amin Hajitou

Abstract readReview
In one paragraph

Review in Molecular therapy. Oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Kaoutar BentayebiCancer Phage Therapy Laboratory, Department of Brain Sciences, Imperial College London, London, UK.
Sara LouatiMedical Biotechnology Laboratory, Faculty of Medicine and Pharmacy, University Mohammed V, Rabat, Morocco.
Keittisak SuwanCancer Phage Therapy Laboratory, Department of Brain Sciences, Imperial College London, London, UK.
Rachid EljaoudiMedical Biotechnology Laboratory, Faculty of Medicine and Pharmacy, University Mohammed V, Rabat, Morocco.
Amin HajitouCancer Phage Therapy Laboratory, Department of Brain Sciences, Imperial College London, London, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Medulloblastoma accounts for approximately 20% of all pediatric brain tumors. Standard treatment typically involves a multimodal approach including surgery, radiation therapy, and chemotherapy. Despite advances in molecular classification and the development of targeted therapies, long-term survival and quality of life remain suboptimal, particularly for patients with high-risk subgroups. Although targeted therapies hold significant promise, their effective delivery to the brain remains a major challenge. The unique cerebellar microenvironment, including the blood-brain barrier, the blood-brain-tumor barrier, and the blood-cerebrospinal fluid barrier, restricts drug penetration and therapeutic efficacy. To overcome these limitations, innovative strategies are being explored to bypass or transiently modulate these barriers in a subgroup- and compartment-specific manner. These approaches include nanoparticle-based delivery systems, focused ultrasound, intrathecal administration, and rational combination therapies. Emerging platforms such as transmorphic phage/adeno-associated virus vectors and lysosomal targeting strategies are under active investigation and may further enhance therapeutic precision. This review provides a comprehensive overview of current brain-targeted drug delivery systems for medulloblastoma, highlighting barrier heterogeneity, recurrence patterns, and emerging technologies with the potential to improve therapeutic efficacy and long-term outcomes for children affected by this aggressive pediatric brain tumor.

Indexed as

central nervous systemcompartment-matched deliverydrug transportgene therapyMT: Special Issue - Advancements in pediatric cancer therapypreclinical modelstranslational science

Identifiers

PMID42199604
PMCPMC13200042

What Socratic holds

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LicenceCC BY
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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.