Evidence map›Paper›PMID 33739852›Full record

ArticleJournal of clinical oncology : official journal of the American Society of Clinical Oncology2021

Favorable Trisomies and

Leonard A Mattano, Meenakshi Devidas, Kelly W Maloney, Cindy Wang, Alison M Friedmann, Patrick Buckley, Michael J Borowitz, Andrew J Carroll, Julie M Gastier-Foster, Nyla A Heerema and 10 more

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06882057 (Chinese Children's Cancer Group-2025 Protocol for Newly Diagnosed Low Risk Childhood B-cell Acute Lymphoblastic Leukemia), which is not on this map. Cited by 25 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 2 pooled it
5.5field-weighted citation impact, top 4% 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.

NCT06882057 phase2 / phase3recruitingnot on this mapstarted 2025, after this paper: background citation

Chinese Children's Cancer Group-2025 Protocol for Newly Diagnosed Low Risk Childhood B-cell Acute Lymphoblastic Leukemia

TypeinterventionalSponsorInstitute of Hematology & Blood Diseases Hospital, ChinaRan2025 to 2033Enrolled3,000ConditionsAcute Lymphoblastic Leukemia ALL, Childhood Leukemia, Acute Lymphoblastic, B Cell Acute Lymphoblastic Leukemia (B-ALL)ArmsBlinatumomab, Reinduction-2 omission, Chemo-light Maintenance 2
3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 2 syntheses or guidelines pooled it, 42 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Article
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  9. Observational
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  12. Review
  13. Genomic Determinants of Outcome in Acute Lymphoblastic Leukemia.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2024
    Article
  14. Review
  15. Article
  16. Article
  17. Prognostic and Pharmacotypic Heterogeneity of Hyperdiploidy in Childhood ALL.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2023
    Article
  18. Haematologica · 2023
    Article
  19. Article
  20. Article
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

20 authors at 18 institutions in 1 country.

Leonard A MattanoHARP Pharma Consulting, Mystic, CT.ORCID 0000-0002-8409-0589
Meenakshi DevidasDepartment of Global Pediatric Medicine, St Jude Children's Research Hospital, Memphis, TN.ORCID 0000-0002-1099-3478
Kelly W MaloneyDepartment of Pediatrics, University of Colorado and Children's Hospital Colorado, Aurora, CO.ORCID 0000-0002-3711-9529
Cindy WangDepartment of Biostatistics, Colleges of Medicine, Public Health, and Health Professions, University of Florida, Gainesville, FL.
Alison M FriedmannDepartment of Pediatrics, Massachusetts General Hospital Cancer Center, Boston, MA.
Patrick BuckleyDepartment of Pathology, Duke University Medical Center, Durham, NC.
Michael J BorowitzDepartment of Pathology, Johns Hopkins University, Baltimore, MD.
Andrew J CarrollDepartment of Genetics, Children's Hospital of Alabama, Birmingham, AL.ORCID 0000-0001-9844-730X
Julie M Gastier-FosterDepartment of Pathology and Laboratory Medicine, Nationwide Children's Hospital, Ohio State University College of Medicine, Columbus, OH.
Nyla A HeeremaDepartment of Pathology, Wexner Medical Center, Ohio State University, Columbus, OH.
Nina S Kadan-LottickDepartment of Pediatrics, Yale University and Yale Cancer Center, New Haven, CT.ORCID 0000-0002-6857-396X
Yousif H MatloubCase Western Reserve University School of Medicine, Cleveland, OH.
David T MarshallDepartment of Radiation Oncology, Medical University of South Carolina, Charleston, SC.ORCID 0000-0002-6029-1538
Linda C StorkDepartment of Pediatrics, Oregon Health and Science University, Portland, OR.
Mignon L LohDepartment of Pediatrics, Benioff Children's Hospital and the Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA.ORCID 0000-0003-4099-4700
Elizabeth A RaetzPerlmutter Cancer Center and Department of Pediatrics, NYU Langone Medical Center, New York, NY.
Brent L WoodDepartments of Pathology and Medicine, University of Washington, Seattle, WA.ORCID 0000-0001-7414-3969
Stephen P HungerDepartment of Pediatrics and The Center for Childhood Cancer Research, Children's Hospital of Philadelphia and the Perelman School of Medicine at The University of Philadelphia, Philadelphia, PA.ORCID 0000-0002-5492-3957
William L CarrollPerlmutter Cancer Center and Department of Pediatrics, NYU Langone Medical Center, New York, NY.
Naomi J WinickDepartment of Pediatrics, UT Southwestern, Simmons Cancer Center, Dallas, TX.ORCID 0000-0002-6636-3870
NYU Langone Health · USAmerican Association of Colleges of Pharmacy · USChildren's Hospital Colorado · USChildren's Hospital of Philadelphia · USChildren's of Alabama · USDuke Medical Center · USJohns Hopkins University · USMassachusetts General Hospital · USMedical University of South Carolina · USNationwide Children's Hospital · USOregon Health & Science University · USSouthwestern Medical Center · USSt. Jude Children's Research Hospital · USThe Ohio State University Wexner Medical Center · USUniversity of California, San Francisco · USUniversity of Washington · USUniversity School · USYale Cancer Center · US

Funding

NCTN BIQSFP ANBL1531 (NRT)U10CA180886 · NCI · PUBLIC HEALTH INSTITUTE · PI Douglas S. Hawkins · 2014 to 2026
$390.6M
COG FOREIGN ACCRUALU10CA098543 · NCI · NATIONAL CHILDHOOD CANCER FOUNDATION · PI ADAMSON, PETER C. · 2003 to 2013
$335.5M
COG SDMC - Statistics CoreU10CA180899 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TODD A ALONZO · 2014 to 2026
$132.8M
Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Children's Oncology Group Statistics &Data Center GrantU10CA098413 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI DEVIDAS, MEENAKSHI · 2003 to 2013
$67.5M
COG U24 Funding 2026-2027U24CA196173 · NCI · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI Mignon Lee-Cheun Loh, Nilsa Del Carmen Ramirez Milan · 2015 to 2026
$62.5M
NCATS NIH HHS UL1 TR001863NCI NIH HHS U10 CA098413NCI NIH HHS U10 CA098543NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899NCI NIH HHS U24 CA196173
6 · The paper itself

Abstract

purposeChildren's Oncology Group (COG) AALL0331 tested whether pegaspargase intensification on a low-intensity chemotherapy backbone would improve the continuous complete remission (CCR) rate in a low-risk subset of children with standard-risk B-acute lymphoblastic leukemia (ALL).

methodsAALL0331 enrolled 5,377 patients with National Cancer Institute standard-risk B-ALL (age 1-9 years, WBC < 50,000/μL) between 2005 and 2010. Following a common three-drug induction, a cohort of 1,857 eligible patients participated in the low-risk ALL random assignment. Low-risk criteria included no extramedullary disease, < 5% marrow blasts by day 15, end-induction marrow minimal residual disease < 0.1%, and favorable cytogenetics (

resultsThe 6-year CCR and overall survival (OS) rates for the entire low-risk cohort were 94.7% ± 0.6% and 98.7% ± 0.3%, respectively. The CCR rates were similar between arms (intensified pegaspargase 95.3% ± 0.8%

conclusionStandard COG therapy without intensified pegaspargase, which can easily be given as an outpatient with limited toxicity, cures nearly all children with B-ALL identified as low-risk by clinical, early response, and favorable cytogenetic criteria.

Indexed as

TrisomyAntineoplastic Combined Chemotherapy ProtocolsChildChild, PreschoolCore Binding Factor Alpha 2 SubunitETS Translocation Variant 6 ProteinFemaleHumansInfantMaleNeoplasm, ResidualOncogene Proteins, FusionPrecursor B-Cell Lymphoblastic Leukemia-LymphomaCore Binding Factor Alpha 2 SubunitETS Translocation Variant 6 ProteinOncogene Proteins, FusionTEL-AML1 fusion protein

Identifiers

PMID33739852
PMCPMC8274747
OpenAlexW3137758248

What OpenQuestion holds

Textmetadata
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Registered trials

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.