Evidence map›Paper›PMID 32304218›Full record

Trial reportNeuro-oncology2020

Excellent outcome of young children with nodular desmoplastic medulloblastoma treated on "Head Start" III: a multi-institutional, prospective clinical trial.

Girish Dhall, Sharon H O'Neil, Lingyun Ji, Kelley Haley, Ashley M Whitaker, Marvin D Nelson, Floyd Gilles, Sharon L Gardner, Jeffrey C Allen, Albert S Cornelius and 11 more

Open access · bronzeAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Neuro-oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 2 pooled it
7.8field-weighted citation impact, top 2% of its field
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

59 citing papers in PubMed, 2 syntheses or guidelines pooled it, 91 citations in OpenAlex.

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  9. Pediatric medulloblastoma.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2026
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 15 institutions in 2 countries.

Girish DhallDivision of Pediatric Hematology-Oncology, University of Alabama Birmingham, Birmingham, Alabama, USA.
Sharon H O'NeilDivision of Neurology and The Saban Research Institute, Children's Hospital Los Angeles (CHLA), Los Angeles, California, USA.
Lingyun JiDepartment of Preventive Medicine, Keck School of Medicine at the University of Southern California, Los Angeles, California, USA.
Kelley HaleyDivision of Hematology-Oncology CHLA, Los Angeles, California, USA.
Ashley M WhitakerDivision of Hematology-Oncology CHLA, Los Angeles, California, USA.
Marvin D NelsonDepartment of Radiology CHLA, Los Angeles, California, USA.
Floyd GillesDepartment of Pathology CHLA, Los Angeles, California, USA.
Sharon L GardnerDivision of Pediatric Hematology-Oncology, NYU Medical Center, New York, New York, USA.
Jeffrey C AllenDivision of Pediatric Hematology-Oncology, NYU Medical Center, New York, New York, USA.
Albert S CorneliusDivision of Pediatric Hematology-Oncology, Helen DeVos Children's Hospital, Grand Rapids, Michigan, USA.
Kamnesh PradhanDivision of Pediatric Hematology-Oncology, Riley Hospital for Children, Indianapolis, Indiana, USA.
James H GarvinDivision of Pediatric Hematology-Oncology, New York Presbyterian Hospital, New York, New York, USA.
Randal S OlshefskiDivision of Pediatric Hematology-Oncology, Nationwide Children's Hospital, Columbus, Ohio, USA.
Juliette HukinDivision of Pediatric Hematology-Oncology, British Columbia Children's Hospital, Vancouver, British Columbia, Canada.
Melanie ComitoDivision of Pediatric Hematology-Oncology, Penn State Hershey Children's Hospital, Hershey, Pennsylvania, USA.
Stewart GoldmanDivision of Pediatric Hematology-Oncology, Lurie Children's Hospital, Chicago, Illinois, USA.
Mark P AtlasDivision of Pediatric Hematology-Oncology, Children's Medical Center of New York, New York, New York, USA.
Andrew W WalterDivision of Pediatric Hematology-Oncology, Alfred I. duPont Hospital for Children, Wilmington, Delaware, USA.
Stephen SandsDepartments of Psychiatry and Behavioral Sciences and Pediatrics, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Richard SpostoDivision of Hematology-Oncology CHLA, Los Angeles, California, USA.
Jonathan L FinlayDivision of Pediatric Hematology-Oncology, Nationwide Children's Hospital, Columbus, Ohio, USA.
APLA Health · USNationwide Children's Hospital · USNYU Langone Health · USAlfred I. duPont Hospital for Children · USBritish Columbia Children's Hospital · CAChildren's Hospital of Los Angeles · USCohen Children's Medical Center · USHelen DeVos Children's Hospital · USLurie Children's Hospital · USMemorial Sloan Kettering Cancer Center · USNewYork–Presbyterian Hospital · USPenn State Milton S. Hershey Medical Center · USRiley Hospital for Children · USUniversity of Alabama at Birmingham · USUniversity of Southern California · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
USC/NORRIS COMPREHENSIVE CANCER CENTER (CORE) SUPPORTP30CA014089 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Fumito Ito · 1985 to 2026
$181.4M
NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA014089
6 · The paper itself

Abstract

background"Head Start" III, was a prospective clinical trial using intensive induction followed by myeloablative chemotherapy and autologous hematopoietic cell rescue (AuHCR) to either avoid or reduce the dose/volume of irradiation in young children with medulloblastoma.

methodsFollowing surgery, patients received 5 cycles of induction followed by myeloablative chemotherapy using carboplatin, thiotepa, and etoposide with AuHCR. Irradiation was reserved for children >6 years old at diagnosis or with residual tumor post-induction.

resultsBetween 2003 and 2009, 92 children <10 years old with medulloblastoma were enrolled. Five-year event-free survival (EFS) and overall survival (OS) rates (±SE) were 46 ± 5% and 62 ± 5% for all patients, 61 ± 8% and 77 ± 7% for localized medulloblastoma, and 35 ± 7% and 52 ± 7% for disseminated patients. Nodular/desmoplastic (ND) medulloblastoma patients had 5-year EFS and OS (±SE) rates of 89 ± 6% and 89 ± 6% compared with 26 ± 6% and 53 ± 7% for classic and 38 ± 13% and 46 ± 14% for large-cell/anaplastic (LCA) medulloblastoma, respectively. In multivariate Cox regression analysis, histology was the only significant independent predictor of EFS after adjusting for stage, extent of resection, regimen, age, and sex (P <0.0001). Five-year irradiation-free EFS was 78 ± 8% for ND and 21 ± 5% for classic/LCA medulloblastoma patients. Myelosuppression was the most common toxicity, with 2 toxic deaths. Twenty-four survivors completed neurocognitive evaluation at a mean of 4.9 years post-diagnosis. IQ and memory scores were within average range overall, whereas processing speed and adaptive functioning were low-average.

conclusionWe report excellent survival and preservation of mean IQ and memory for young children with ND medulloblastoma using high-dose chemotherapy, with most patients surviving without irradiation.

Indexed as

Cerebellar NeoplasmsEarly Intervention, EducationalMedulloblastomaAntineoplastic Combined Chemotherapy ProtocolsCarboplatinChildChild, PreschoolCombined Modality TherapyFemaleHumansMaleProspective StudiesSurvival RateCarboplatindesmoplasticinfantsmedulloblastomamyeloablative chemotherapy

Identifiers

PMID32304218
PMCPMC7746930
OpenAlexW3016851479

What OpenQuestion holds

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Registered trials

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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.