Evidence map›Paper›PMID 42622719›Full record

Observational studyChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2026

Reirradiation for diffuse intrinsic pontine glioma in an upper middle-income country: does full dose improve outcomes?

Natália Dassi, Maria Luisa Sucharski Figueiredo, Francine Tesser Gamba, Marcos Devanir Silva da Costa, Ana Carolina Dos Santos Torquato, Jessica Benigno Rodrigues, Ronaldo Modesto de Souza Filho, Sergio Cavalheiro, Patricia Alessandra Dastoli, Frederico Adolfo Silva and 5 more

Abstract readObservational Study
In one paragraph

Observational study in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 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

15 authors.

Natália DassiDepartment of Pediatric Oncology, IOP-GRAACC-Federal University of Sao Paulo, Pedro de Toledo Street, 572, Sao Paulo, 04039001, Brazil. natalia.dassi@unifesp.br.
Maria Luisa Sucharski FigueiredoDepartment of Radiation Oncology, IOP-GRAACC-Federal University of Sao Paulo, Sao Paulo, Brazil.
Francine Tesser GambaGenetics Laboratory, IOP-GRAACC-Federal University of Sao Paulo, Sao Paulo, Brazil.
Marcos Devanir Silva da CostaDepartment of Neurosurgical Oncology, IOP-GRAACC-Federal University of Sao Paulo, Sao Paulo, Brazil.
Ana Carolina Dos Santos TorquatoDepartment of Pediatric Oncology, IOP-GRAACC-Federal University of Sao Paulo, Pedro de Toledo Street, 572, Sao Paulo, 04039001, Brazil.
Jessica Benigno RodriguesDepartment of Pediatric Oncology, IOP-GRAACC-Federal University of Sao Paulo, Pedro de Toledo Street, 572, Sao Paulo, 04039001, Brazil.
Ronaldo Modesto de Souza FilhoDepartment of Pathology , IOP-GRAACC-Federal University of Sao Paulo, Sao Paulo, Brazil.
Sergio CavalheiroDepartment of Neurosurgical Oncology, IOP-GRAACC-Federal University of Sao Paulo, Sao Paulo, Brazil.
Patricia Alessandra DastoliDepartment of Neurosurgical Oncology, IOP-GRAACC-Federal University of Sao Paulo, Sao Paulo, Brazil.
Frederico Adolfo SilvaDepartment of Oncologic Radiology, IOP-GRAACC-Federal University of Sao Paulo, Sao Paulo, Brazil.
Carlota Vitoria Blassioli MoraesDepartment of Pediatric Oncology, IOP-GRAACC-Federal University of Sao Paulo, Pedro de Toledo Street, 572, Sao Paulo, 04039001, Brazil.
Silvia Regina Caminada de ToledoGenetics Laboratory, IOP-GRAACC-Federal University of Sao Paulo, Sao Paulo, Brazil.
Nasjla Saba Da SilvaDepartment of Pediatric Oncology, IOP-GRAACC-Federal University of Sao Paulo, Pedro de Toledo Street, 572, Sao Paulo, 04039001, Brazil.
Michael Jenwei ChenDepartment of Radiation Oncology, IOP-GRAACC-Federal University of Sao Paulo, Sao Paulo, Brazil.
Andrea Maria CappellanoDepartment of Pediatric Oncology, IOP-GRAACC-Federal University of Sao Paulo, Pedro de Toledo Street, 572, Sao Paulo, 04039001, Brazil. andreacappellano@graacc.org.br.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeReirradiation (reRT) during diffuse intrinsic pontine glioma (DIPG) progression has emerged as a potential treatment strategy for prolonging survival.

methodsThis retrospective, single-center observational study was conducted on children diagnosed with DIPG between 2010 and 2025, and data from 58 were collected. Doses for reRT were as follows: 50-54 Gy (1.8-2.0 Gy daily/fractions) or 39 Gy (3 Gy daily/fractions). Overall survival (OS) was defined as the time from diagnosis to the date of death and reRT OS, reirradiation starting to death. The Kaplan-Meier method and log-rank test were used for survival analysis.

resultsThe median age was 7.1 years (range 2.9-16.2 years). Twenty-six patients underwent a biopsy. The H3K27M mutation was the most prevalent in our study, followed by TP53 altered gene. Twenty-two patients underwent reRT at progression. The median time from initial treatment to reRT was 9.9 months (range 6.7 to 20.5 months). Seven of the 22 patients received reRT at a dose of 39 Gy while 14 at doses of 50-54 Gy. The median OS from reRT to death was 5.8 months (range, 0.9-18.3 months). Patients who received reRT had a longer OS compared to those who did not (median OS of 17.9 versus 9.8 months; p = 0.005). Longer time for progression (> 9 months) and dose of reRT > 50 Gy were statistically significantly correlated with better OS. Reirradiation was generally well-tolerated by all patients.

conclusionsThis study offers molecular insights into this tumor type and presents a therapeutic option with higher nominal doses reRT within a palliative context to prolong survival of these patients.

Indexed as

Brain Stem NeoplasmsDiffuse Intrinsic Pontine GliomaRe-IrradiationAdolescentChildChild, PreschoolFemaleHumansMaleRetrospective StudiesTreatment OutcomeDiffuse intrinsic pontine gliomaMolecular alterationsTumor biopsy

Identifiers

PMID42622719
PMCPMC13493434

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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.