Evidence map›Paper›PMID 40406256›Full record

ArticleFrontiers in oncology2025

Optimal fractionation scheme for lymphocyte infiltration in glioblastoma multiforme radiotherapy.

Lorea Iturri, Cristéle Gilbert, Julie Espenon, Annaïg Bertho, Sarah Potiron, Marjorie Juchaux, Yolanda Prezado

Abstract read
In one paragraph

Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Lorea IturriInstitut Curie, Université Paris Sciences et Lettres (PSL), Centre National pour la recherche scientifique (CNRS) Unité mixte de recherche (UMR3347), Inserm U1021, Signalisation Radiobiologie et Cancer, Orsay, France.
Cristéle GilbertInstitut Curie, Université Paris Sciences et Lettres (PSL), Centre National pour la recherche scientifique (CNRS) Unité mixte de recherche (UMR3347), Inserm U1021, Signalisation Radiobiologie et Cancer, Orsay, France.
Julie EspenonInstitut Curie, Université Paris Sciences et Lettres (PSL), Centre National pour la recherche scientifique (CNRS) Unité mixte de recherche (UMR3347), Inserm U1021, Signalisation Radiobiologie et Cancer, Orsay, France.
Annaïg BerthoInstitut Curie, Université Paris Sciences et Lettres (PSL), Centre National pour la recherche scientifique (CNRS) Unité mixte de recherche (UMR3347), Inserm U1021, Signalisation Radiobiologie et Cancer, Orsay, France.
Sarah PotironInstitut Curie, Université Paris Sciences et Lettres (PSL), Centre National pour la recherche scientifique (CNRS) Unité mixte de recherche (UMR3347), Inserm U1021, Signalisation Radiobiologie et Cancer, Orsay, France.
Marjorie JuchauxInstitut Curie, Université Paris Sciences et Lettres (PSL), Centre National pour la recherche scientifique (CNRS) Unité mixte de recherche (UMR3347), Inserm U1021, Signalisation Radiobiologie et Cancer, Orsay, France.
Yolanda PrezadoInstitut Curie, Université Paris Sciences et Lettres (PSL), Centre National pour la recherche scientifique (CNRS) Unité mixte de recherche (UMR3347), Inserm U1021, Signalisation Radiobiologie et Cancer, Orsay, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Radioresistant and immunosuppressive tumors, such as glioblastoma multiforme (GBM), remain a challenge, as current clinical approaches-surgical resection and chemoradiation-do not yet provide effective treatment. Materials and methods: Two orthotopic rat glioma models with differing vascularization and immunogenicity were irradiated with three dose fractionation schemes. Tumor immune cell populations were analyzed by flow cytometry. Results: A single high dose (25 Gy) or extreme hypofractionation is required to elicit a significant immune infiltration in tumors. Conclusions: Using RT as an immune primer in GBM would require very high and toxic doses with conventional RT methods. While 25 Gy is used in conventional stereotactic radiosurgery, such a high dose is typically limited to small brain volumes. Novel approaches, such as FLASH-RT or minibeam RT, offer alternatives to mitigate toxicity while achieving the required doses.

Indexed as

fractionationgliomainfiltrationlymphocytesradiotherapy

Identifiers

PMID40406256
PMCPMC12095198

What Socratic holds

Textmetadata
LicenceCC BY
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.