Evidence map›Paper›PMID 32105509›Full record

ArticleJournal of clinical oncology : official journal of the American Society of Clinical Oncology2020

Efficacy of High-Dose Chemotherapy and Three-Dimensional Conformal Radiation for Atypical Teratoid/Rhabdoid Tumor: A Report From the Children's Oncology Group Trial ACNS0333.

Alyssa T Reddy, Douglas R Strother, Alexander R Judkins, Peter C Burger, Ian F Pollack, Mark D Krailo, Allen B Buxton, Chris Williams-Hughes, Maryam Fouladi, Anita Mahajan and 12 more

Open access · greenAbstract read
In one paragraph

Article in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 108 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
108citing papers in PubMed, 1 pooled it
8.2field-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

108 citing papers in PubMed, 1 synthesis or guideline pooled it, 184 citations in OpenAlex.

  1. Pooled it
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  5. Recurrent C19MC-altered embryonal tumors with multilayered rosettes: outcomes of stereotactic radiosurgery.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2026
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  10. Machine learning-driven conditional survival prediction model for atypical teratoid/rhabdoid tumor.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2026
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48 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 18 institutions in 3 countries.

Alyssa T ReddyDepartments of Neurology and Pediatrics, University of California San Francisco, San Francisco, CA.
Douglas R StrotherCumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Alexander R JudkinsDepartment of Pathology and Laboratory Medicine, Children's Hospital Los Angeles; Keck School of Medicine, University of Southern California, Los Angeles, CA.
Peter C BurgerDepartment of Pathology, Johns Hopkins University, Baltimore, MD.
Ian F PollackDepartment Neurosurgery, UPMC Children's Hospital of Pittsburgh, Pittsburgh, PA.
Mark D KrailoDepartment of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA.
Allen B BuxtonChildren's Oncology Group, Monrovia, CA.
Chris Williams-HughesChildren's Oncology Group, Monrovia, CA.
Maryam FouladiDepartment of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Anita MahajanDepartment of Radiation Oncology, Mayo Clinic, Rochester, MN.
Thomas E MerchantDepartment of Radiation Oncology, St Jude Children's Research Hospital, Memphis, TN.
Ben HoDepartment of Cell Biology, Hospital for Sick Children, Toronto, Ontario, Canada.
Claire M MazewskiAflac Cancer & Blood Disorders Center, Children's Healthcare of Atlanta; Department of Pediatrics, Emory University School of Medicine, Atlanta, GA.
Victor A LewisCumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Amar GajjarDepartment of Oncology, St Jude Children's Research Hospital, Memphis, TN.
Louis-Gilbert VezinaDepartment of Radiology, The George Washington University School Medicine and Health Sciences, Washington, DC.
Timothy N BoothDepartment of Radiology, University of Texas Southwestern, Dallas, TX.
Kerry W ParsonsAstraZeneca Pharmaceuticals, Cambridge, UK.
Vicky L PossDepartment of Pediatrics, University of Alabama at Birmingham, Birmingham, AL.
Tianni ZhouDepartment of Mathematics and Statistics, California State University at Long Beach, Long Beach, CA.
Jaclyn A BiegelDepartment of Pathology and Laboratory Medicine, Children's Hospital Los Angeles; Keck School of Medicine, University of Southern California, Los Angeles, CA.
Annie HuangDepartment of Pediatrics, Hospital for Sick Children, Arthur and Sonia Labatt Brain Tumour Research Centre, Toronto, Ontario, Canada.
Children's Oncology Group · USSt. Jude Children's Research Hospital · USUniversity of Calgary · CAUniversity of Southern California · USAstraZeneca (United Kingdom) · GBCalifornia State University, Long Beach · USChildren's Healthcare of Atlanta · USChildren's Hospital of Los Angeles · USChildren's Hospital of Pittsburgh · USCincinnati Children's Hospital Medical Center · USGeorge Washington University · USHospital for Sick Children · CAJohns Hopkins University · USMayo Clinic in Arizona · USSickKids Foundation · CAThe University of Texas Southwestern Medical Center · USUniversity of Alabama at Birmingham · USUniversity of California, San Francisco · US

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
MOLECULAR CYTOGENETICS: PEDIATRIC CNS TUMORSR01CA046274 · NCI · CHILDREN'S HOSP OF PHILADELPHIA · PI BIEGEL, JACLYN A · 1989 to 2012
$2.7M
NCI NIH HHS R01 CA046274NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899
6 · The paper itself

Abstract

purposeAtypical teratoid/rhabdoid tumor (AT/RT) is an aggressive, early-childhood brain tumor without standard effective treatment. To our knowledge, we conducted the first AT/RT-specific cooperative group trial, ACNS0333, to examine the efficacy and safety of intensive postoperative chemotherapy and focal radiation to treat AT/RT. PATIENTS AND

methodsPatients from birth to 22 years of age with AT/RT were eligible. After surgery, they received 2 courses of multiagent chemotherapy, followed by 3 courses of high-dose chemotherapy with peripheral blood stem cell rescue and involved-field radiation therapy. Timing of radiation was based on patient age and disease location and extent. Central testing of tumor and blood for

resultsOf 65 evaluable patients, 54 were < 36 months of age. ACNS0333 therapy significantly reduced the risk of EFS events in patients < 36 months of age compared with the historical cohort (

conclusionThe ACNS0333 regimen dramatically improved survival compared with historical therapies for patients with AT/RT. Clinical characteristics and molecular subgrouping suggest prognostic differences. ACNS0333 results lay a foundation on which to build future studies and incorporate testing of new therapeutic agents.

Indexed as

AdolescentAntineoplastic Combined Chemotherapy ProtocolsChildChild, PreschoolCombined Modality TherapyFemaleHumansInfantInfant, NewbornMalePrognosisRadiotherapy, ConformalRhabdoid TumorSMARCB1 ProteinTeratomaYoung AdultSMARCB1 ProteinSMARCB1 protein, human

Identifiers

PMID32105509
PMCPMC7145589
OpenAlexW3008366344

What OpenQuestion holds

Textmetadata
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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 OpenQuestion graph.