Evidence map›Paper›PMID 41885589›Full record

ArticleNeuro-oncology2026

Cumulative dose of chemotherapy and survival outcomes in children with average-risk medulloblastoma treated on Children's Oncology Group study ACNS0331.

Erin Wright, Catherine Billups, Sarah Rush, Yimei Li, Anna Janns, Jeff M Michalski, Ralph Salloum, Peter de Blank

Abstract read
In one paragraph

Article in Neuro-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.

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0citing papers in PubMed
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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

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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

5 · Who and what money

Authors and funding

8 authors.

Erin WrightDepartment of Hematology-Oncology, Akron Children's Hospital, Akron, Ohio.ORCID 0000-0001-5044-058X
Catherine BillupsDepartment of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee.ORCID 0000-0003-2819-4946
Sarah RushDepartment of Hematology-Oncology, Akron Children's Hospital, Akron, Ohio.ORCID 0000-0002-3416-7031
Yimei LiDepartment of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee.ORCID 0000-0002-7046-4316
Anna JannsDepartment of Pediatrics, Emory School of Medicine, Atlanta, Georgia.
Jeff M MichalskiDepartment of Radiation Oncology, Washington University School of Medicine, St. Louis, Missouri.ORCID 0000-0003-0563-3766
Ralph SalloumDepartment of Hematology-Oncology, Boston Children's Hospital/Dana Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0001-9437-0616
Peter de BlankDepartment of Oncology, University of Cincinnati School of Medicine and Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.ORCID 0000-0001-6623-3040

Funding

NCTN BIQSFP ANBL1531 (NRT)U10CA180886 · NCI · PUBLIC HEALTH INSTITUTE · PI Douglas S. Hawkins · 2014 to 2026
$390.6M
COG SDMC - Statistics CoreU10CA180899 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TODD A ALONZO · 2014 to 2026
$132.8M
Bogniard Family Neuro-Oncology Fund at Akron Children's HospitalNCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899NIH HHS U10CA180886NIH HHS U10CA180899
6 · The paper itself

Abstract

backgroundAlthough survival outcomes for average-risk (AR) medulloblastoma remain excellent, patients experience significant long-term toxicities. To evaluate the effect of therapy dose modifications among children with AR medulloblastoma, we examined the association of cumulative chemotherapy dose with overall survival (OS) and event-free survival (EFS) for patients treated on Children's Oncology Group (COG) study ACNS0331.

methodsA cohort of children enrolled on ACNS0331 (medulloblastoma confirmed by methylation, received standard dose craniospinal radiation, and completed all cycles of chemotherapy) were evaluated for cumulative chemotherapy dose intensity continuously and categorically (≥75% or <75% of planned dose). Cox proportional hazards regression models were used to examine associations of proportion of planned chemotherapy received with outcome. A secondary analysis separately evaluated each of the 4 molecular subgroups: Wnt-activated (WNT), Sonic Hedgehog Activated (SHH), group 3 and group 4.

resultsTwo hundred thirty-five children were followed for a median of 9.3 years (range, 7.0-10.4). Dose intensities of vincristine (VCR) and cisplatin showed the most variability (17% and 23.8% of patients received <75% of expected dosing, respectively). Molecular subgroup remained a significant predictor of outcome (EFS [P = .012] and OS [P = .008]). Cyclophosphamide and lomustine were not examined due to minimal dose variability. No significant differences in EFS or OS were found related to reduced dose intensity for VCR (P = .49 EFS, P = .52 OS) or cisplatin (P = .36 EFS, P = .35 OS) when analyzed independently. There was no difference in the effect of dose reductions by molecular subgroup.

conclusionsModerate dose reductions of at least 25% in VCR and cisplatin do not significantly affect survival in AR medulloblastoma. Effects of larger dose reductions (>50%) or dose reductions in high-risk disease were not studied.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCerebellar NeoplasmsMedulloblastomaAdolescentChildChild, PreschoolCisplatinFemaleFollow-Up StudiesHumansMalePrognosisSurvival RateVincristineCisplatinVincristineaverage-risk medulloblastomacisplatinvincristine

Identifiers

PMID41885589
PMCPMC13338335

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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.