Evidence map›Paper›PMID 37257143›Full record

Trial reportJournal of clinical oncology : official journal of the American Society of Clinical Oncology2023

Children's Oncology Group AALL1331: Phase III Trial of Blinatumomab in Children, Adolescents, and Young Adults With Low-Risk B-Cell ALL in First Relapse.

Laura E Hogan, Patrick A Brown, Lingyun Ji, Xinxin Xu, Meenakshi Devidas, Teena Bhatla, Michael J Borowitz, Elizabeth A Raetz, Andrew Carroll, Nyla A Heerema and 8 more

3 registry-linked trialsOpen access · greenAbstract readRandomized Controlled TrialClinical Trial, Phase III
In one paragraph

Trial report in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 65 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed, 2 pooled it
23.8field-weighted citation impact, top 1% 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.

NCT02101853 phase3active not recruitingnot on this map

Risk-Stratified Randomized Phase III Testing of Blinatumomab (NSC#765986) in First Relapse of Childhood B-Lymphoblastic Leukemia (B-ALL)

TypeinterventionalSponsorNational Cancer Institute (NCI)Ran2014 to 2026Enrolled669ConditionsRecurrent B Acute Lymphoblastic LeukemiaArmsAllogeneic Hematopoietic Stem Cell Transplantation, Asparaginase, Blinatumomab, Cyclophosphamide, Cytarabine
NCT06607419 phase2 / phase3recruitingnot on this mapstarted 2024, after this paper: background citation

Efficacy Study of Blinatumomab Clean Up Early Residual Disease for Newly Diagnosed Pediatric B Lymphoblastic Leukemia

TypeinterventionalSponsorShanghai Jiao Tong University School of MedicineRan2024 to 2030Enrolled90ConditionsB-Cell Lymphoblastic LeukemiaArmsBlinatumomab
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

65 citing papers in PubMed, 2 syntheses or guidelines pooled it, 82 citations in OpenAlex.

  1. Guideline
  2. Guideline
  3. Trial
  4. Trial
  5. Observational
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Targeted therapies in pediatric oncology: A start.Molecular therapy. Oncology · 2026
    Review
  20. Article

5 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 18 institutions in 3 countries.

Laura E HoganDepartment of Pediatrics, Stony Brook Children's, Stony Brook, NY.ORCID 0000-0001-8841-3296
Patrick A BrownBristol Myers Squibb, Princeton, NJ.
Lingyun JiDepartment of Population and Public Health Sciences, Keck School of Medicine, University of Southern California, Los Angeles, CA.ORCID 0000-0003-2500-1993
Xinxin XuChildren's Oncology Group, Monrovia, CA.
Meenakshi DevidasDepartment of Global Pediatric Medicine, St Jude Children's Research Hospital, Memphis, TN.
Teena BhatlaChildrens Hospital of New Jersey at Newark Beth Israel, Newark, NJ.
Michael J BorowitzDepartments of Pathology and Oncology, Johns Hopkins University School of Medicine, Baltimore, MD.
Elizabeth A RaetzDepartment of Pediatrics, NYU Langone Health, New York, NY.ORCID 0000-0002-8547-1658
Andrew CarrollUniversity of Alabama at Birmingham, Birmingham, AL.ORCID 0000-0001-9844-730X
Nyla A HeeremaDepartment of Pathology, The Ohio State University, Columbus, OH.
Gerhard ZugmaierAmgen Research (Munich), GmbH, Munich, Germany.
Elad SharonDivision of Cancer Treatment and Diagnosis, National Cancer Institute, Cancer Therapy Evaluation Program, Bethesda, MD.ORCID 0000-0002-0044-9719
Melanie B BernhardtSection of Hematology/Oncology, Department of Pediatrics, Baylor College of Medicine, Houston, TX.ORCID 0000-0002-9612-3624
Stephanie A TerezakisDepartment of Radiation Oncology, University of Minnesota, Minneapolis, MN.ORCID 0000-0002-8125-3987
Lia GoreUniversity of Colorado School of Medicine and Center for Cancer and Blood Disorders, Children's Hospital Colorado, Aurora, CO.ORCID 0000-0002-2546-4616
James A WhitlockHospital for Sick Children and University of Toronto, Toronto, Canada.ORCID 0000-0002-7887-0634
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 Pennsylvania, Philadelphia, PA.ORCID 0000-0002-5492-3957
Mignon L LohBen Towne Center for Childhood Cancer Research, Seattle Children's Research Institute, Seattle, WA.
Amgen (Germany) · DEBaylor College of Medicine · USBristol-Myers Squibb (United States) · USChildren's Hospital Colorado · USChildren's Hospital of Philadelphia · USChildren's Oncology Group · USJohns Hopkins University · USNational Cancer Institute · USNewark Beth Israel Medical Center · USNYU Langone Health · USSeattle Children's Hospital · USSt. Jude Children's Research Hospital · USStony Brook Children's Hospital · USThe Ohio State University · USUniversity of Alabama at Birmingham · USUniversity of Minnesota · USUniversity of Southern California · USUniversity of Toronto · CA

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
NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899
6 · The paper itself

Abstract

purposeBlinatumomab, a bispecific T-cell engager immunotherapy, is efficacious in relapsed/refractory B-cell ALL (B-ALL) and has a favorable toxicity profile. One aim of the Children's Oncology Group AALL1331 study was to compare survival of patients with low-risk (LR) first relapse of B-ALL treated with chemotherapy alone or chemotherapy plus blinatumomab. PATIENTS AND

methodsAfter block 1 reinduction, patients age 1-30 years with LR first relapse of B-ALL were randomly assigned to block 2/block 3/two continuation chemotherapy cycles/maintenance (arm C) or block 2/two cycles of continuation chemotherapy intercalated with three blinatumomab blocks/maintenance (arm D). Patients with CNS leukemia received 18 Gy cranial radiation during maintenance and intensified intrathecal chemotherapy. The primary and secondary end points were disease-free survival (DFS) and overall survival (OS).

resultsThe 4-year DFS/OS for the 255 LR patients accrued between December 2014 and September 2019 were 61.2% ± 5.0%/90.4% ± 3.0% for blinatumomab versus 49.5% ± 5.2%/79.6% ± 4.3% for chemotherapy (

conclusionFor children, adolescents, and young adults with B-ALL in LR first relapse, there was no statistically significant difference in DFS or OS between the blinatumomab and standard chemotherapy arms overall. However, blinatumomab significantly improved DFS and OS for the two thirds of patients with BM ± EM relapse, establishing a new standard of care for this population. By contrast, similar outcomes and poor DFS for both arms were observed in the one third of patients with IEM; new treatment approaches are needed for these patients (ClinicalTrials.gov identifier: NCT02101853).

Indexed as

Antibodies, BispecificAntineoplastic AgentsAdolescentAdultChildChild, PreschoolDisease-Free SurvivalHumansInfantRecurrenceYoung AdultAntibodies, BispecificAntineoplastic Agentsblinatumomab

Identifiers

PMID37257143
PMCPMC10852366
OpenAlexW4378802651

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.