Evidence map›Paper›PMID 42709436›Full record

ArticleJAMA network open2026

Blinatumomab Care Delivery for Pediatric B-Cell Acute Lymphoblastic Leukemia.

Daniel J Zheng, Katelyn Oranges, Subhash Ramakrishnan, Lingyun Ji, Melissa P Beauchemin, Sarah W Alexander, Allison Barz Leahy, Kira Bona, Emi H Caywood, Sharon M Castellino and 13 more

Abstract read
In one paragraph

Article in JAMA network open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

23 authors.

Daniel J ZhengUniversity of Pennsylvania, Philadelphia.
Katelyn OrangesDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Subhash RamakrishnanChildren's Oncology Group, Monrovia, California.
Lingyun JiDepartment of Population and Public Health Sciences, Keck School of Medicine, University of Southern California, Los Angeles.
Melissa P BeaucheminColumbia University Irving Medical Center, New York, New York.
Sarah W AlexanderDivision of Hematology, Oncology and Bone Marrow Transplant, BC Children's Hospital, Vancouver, Canada.
Allison Barz LeahyUniversity of Pennsylvania, Philadelphia.
Kira BonaDana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, Massachusetts.
Emi H CaywoodDepartment of Pediatrics, Thomas Jefferson University, Philadelphia, Pennsylvania.
Sharon M CastellinoAflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Winship Cancer Institute, Emory University, Atlanta, Georgia.
Sumit GuptaDivision of Hematology/Oncology, The Hospital for Sick Children, Toronto, Canada.
Douglas S HawkinsSeattle Children's Hospital, University of Washington, Seattle.
Olga MilitanoChildren's Oncology Group, Monrovia, California.
Kathleen E MontgomeryUniversity of Wisconsin-Madison School of Nursing.
Haley NewmanUniversity of Pennsylvania, Philadelphia.
Rachel E RauBen Towne Center for Childhood Cancer and Blood Disorders Research, Seattle Children's Hospital, Seattle, Washington.
Susan RheingoldUniversity of Pennsylvania, Philadelphia.
Joanna M RoblesWake Forest University School of Medicine, Winston Salem, North Carolina.
Michael E RothMD Anderson Cancer Center, Houston, Texas.
David TeacheyUniversity of Pennsylvania, Philadelphia.
Sarah VargasChildren's Oncology Group, Monrovia, California.
Sue ZupanecThe Hospital for Sick Children, Toronto, Ontario, Canada.
Susan K ParsonsTufts Medical Center, Boston, Massachusetts.

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

Importance: Blinatumomab, a novel immunotherapy administered as a 28-day continuous infusion, has fundamentally shifted the treatment paradigm for pediatric B-cell acute lymphoblastic leukemia (B-ALL) and is now considered a component of standard therapy for the most common childhood cancer. However, the care delivery challenges in transitioning from an experimental agent on a clinical trial to widespread clinical implementation are unknown. Objective: To characterize the clinical landscape of pediatric blinatumomab care-delivery practice and challenges in the US from the perspective of treating centers. Design, Setting, and Participants: This survey study was conducted from February to March 2025 among US member institutions of the Children's Oncology Group (COG) across 44 states. Exposure: Institutional characteristics, including participation in the National Cancer Institute Community Oncology Research Program (NCORP), US census region, site-reported annual pediatric ALL patient volume, and prior blinatumomab experience, were assessed. Main Outcomes and Measures: Incorporation of blinatumomab as standard therapy by pediatric B-ALL subtype; major outpatient care-delivery challenges defined as 4 or 5 on a 5-point Likert scale by more than 25% of centers. Results: Of 195 active US COG member institutions, 147 centers completed the survey and were successfully matched with a unique COG identifier, among which 35 institutions (23.8%) were NCORP participants. There were 32 institutions (21.8%) in Midwest, 30 institutions (20.4%) in Northeast, 60 institutions (40.8%) in South, and 25 institutions (17.0%) in West census regions. Most centers reported using blinatumomab as their institutional standard therapy for National Cancer Institute standard risk-average (134 centers [91.2%]), standard risk-high (144 centers [98.0%]), and high-risk (140 centers [95.2%]) B-ALL. Fewer centers reported using blinatumomab for infant (83 centers [56.5%]) or Philadelphia chromosome-positive (96 centers [65.3%]) B-ALL. The most common major outpatient blinatumomab site care-delivery challenges included lack of home care companies (75 centers [51.0%]), family distance to treating center (41 centers [27.9%]), and insurance coverage for home care companies (37 centers [25.2%]). There were 67 sites (45.6%) that reported having no home care company options for any patients. Conclusions and Relevance: In this study, challenges associated with pediatric blinatumomab home care were highly prevalent, with broader implications for health system infrastructure availability. These data highlight a need to plan for clinical implementation strategies alongside the development and testing of novel therapies.

Indexed as

Antibodies, BispecificAntineoplastic AgentsDelivery of Health CarePrecursor B-Cell Lymphoblastic Leukemia-LymphomaAdolescentChildChild, PreschoolFemaleHumansInfantMaleUnited StatesAntibodies, BispecificAntineoplastic Agentsblinatumomab

Identifiers

PMID42709436
PMCPMC13555368

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.