Evidence map›Paper›PMID 38822537›Full record

ArticlePediatric blood & cancer2024

Long-term follow-up of patients with intermediate-risk neuroblastoma treated with response- and biology-based therapy: A report from the Children's Oncology Group study ANBL0531.

Erin K Barr, Arlene Naranjo, Clare J Twist, Sheena C Tenney, Mary Lou Schmidt, Wendy B London, Julie Gastier-Foster, E Stanton Adkins, Peter Mattei, Michael H Handler and 5 more

Abstract read
In one paragraph

Article in Pediatric blood & cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

15 authors.

Erin K BarrDepartment of Pediatrics, Texas Tech University Health Sciences, Lubbock, Texas, USA.
Arlene NaranjoDepartment of Biostatistics, University of Florida Children's Oncology Group Statistics and Data Center, Gainesville, Florida, USA.
Clare J TwistRoswell Park Comprehensive Cancer Center, Buffalo, New York, USA.
Sheena C TenneyDepartment of Biostatistics, University of Florida Children's Oncology Group Statistics and Data Center, Gainesville, Florida, USA.
Mary Lou SchmidtDepartment of Pediatrics, University of Illinois at Chicago, Chicago, Illinois, USA.
Wendy B LondonDana-Farber/Boston Children's Cancer and Blood Disorders Center, Harvard Medical School, Boston, Massachusetts, USA.ORCID 0000-0003-3571-6538
Julie Gastier-FosterDepartment of Pediatrics and Pathology/Immunology, Baylor College of Medicine, Houston, Texas, USA.
E Stanton AdkinsDepartment of Pediatrics, Palmetto Health-USC Medical Group, Columbia, South Carolina, USA.
Peter MatteiDepartment of Surgery, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Michael H HandlerDepartment of Neurosurgery, Children's Hospital Colorado, Aurora, Colorado, USA.
Katherine K MatthayDepartment of Pediatrics, University of California San Francisco School of Medicine, San Francisco, California, USA.ORCID 0000-0002-0146-2499
Julie R ParkDepartment of Oncology, St.Jude Children's Research Hospital, Memphis, Tennessee, USA.
John M MarisDepartment of Pediatrics, Children's Hospital of Philadelphia and Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA.ORCID 0000-0002-8088-7929
Ami V DesaiDepartment of Pediatrics, University of Chicago, Chicago, Illinois, USA.
Susan L CohnDepartment of Pediatrics, University of Chicago, Chicago, Illinois, USA.ORCID 0000-0001-5749-7650

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
Discovering mechanisms of neuroblastoma tumorigenesis to improve patient outcomesR35CA220500 · NCI · CHILDREN'S HOSP OF PHILADELPHIA · PI JOHN M MARIS · 2017 to 2026
$8.7M
NCI NIH HHS R35 CA220500NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899NCTN Operations Center U10CA180886St. Baldrick's Foundation
6 · The paper itself

Abstract

backgroundWe previously reported excellent three-year overall survival (OS) for patients with newly diagnosed intermediate-risk neuroblastoma treated with a biology- and response-based algorithm on the Children's Oncology Group study ANBL0531. We now present the long-term follow-up results.

methodsAll patients who met the age, stage, and tumor biology criteria for intermediate-risk neuroblastoma were eligible. Treatment was based on prognostic biomarkers and overall response. Event-free survival (EFS) and OS were estimated by the Kaplan-Meier method.

resultsThe 10-year EFS and OS for the entire study cohort (n = 404) were 82.0% (95% confidence interval (CI), 77.2%-86.9%) and 94.7% (95% CI, 91.8%-97.5%), respectively. International Neuroblastoma Staging System stage 4 patients (n = 133) had inferior OS compared with non-stage 4 patients (n = 271; 10-year OS: 90.8% [95% CI, 84.5%-97.0%] vs 96.6% [95% CI, 93.9%-99.4%], p = .02). Infants with stage 4 tumors with ≥1 unfavorable biological feature (n = 47) had inferior EFS compared with those with favorable biology (n = 61; 10-year EFS: 66.8% [95% CI, 50.4%-83.3%] vs 86.9% [95% CI, 76.0%-97.8%], p = .02); OS did not differ (10-year OS: 84.4% [95% CI, 71.8%-97.0%] vs 95.0% [95% CI, 87.7%-100.0%], p = .08). Inferior EFS but not OS was observed among patients with tumors with (n = 26) versus without (n = 314) 11q loss of heterozygosity (10-year EFS: 68.4% [95% CI, 44.5%-92.2%] vs 83.9% [95% CI, 78.7%-89.2%], p = .03; 10-year OS: 88.0% [95% CI, 72.0%-100.0%] vs 95.7% [95% CI, 92.8%-98.6%], p = .09).

conclusionsThe ANBL0531 trial treatment algorithm resulted in excellent long-term survival. More effective treatments are needed for subsets of patients with unfavorable biology tumors.

Indexed as

NeuroblastomaAdolescentAntineoplastic Combined Chemotherapy ProtocolsChildChild, PreschoolFemaleFollow-Up StudiesHumansInfantInfant, NewbornMaleNeoplasm StagingPrognosisSurvival RateIntermediate risklong‐term follow‐upneuroblastomaoutcomes

Identifiers

PMID38822537
PMCPMC11318088

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