Evidence map›Paper›PMID 38689540›Full record

ArticlePediatric blood & cancer2024

Late cognitive and adaptive outcomes of patients with neuroblastoma-associated opsoclonus-myoclonus-ataxia-syndrome: A report from the Children's Oncology Group.

Prerna Kumar, Victoria W Willard, Leanne Embry, Arlene Naranjo, Brian LaBarre, Katherine K Matthay, Pedro A de Alarcon

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

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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

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

7 authors.

Prerna KumarPediatrics, University of Illinois College of Medicine Peoria, Peoria, Illinois, USA.ORCID 0009-0004-5688-8229
Victoria W WillardPsychology & Biobehavioral Sciences, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.ORCID 0000-0003-3340-1460
Leanne EmbryPediatrics, UT Health San Antonio, San Antonio, Texas, USA.ORCID 0000-0002-4853-6643
Arlene NaranjoBiostatistics, Children's Oncology Group Statistics & Data Center, University of Florida, Gainesville, Florida, USA.
Brian LaBarreBiostatistics, Children's Oncology Group Statistics & Data Center, University of Florida, Gainesville, Florida, USA.
Katherine K MatthayPediatric Oncology, University of California San Francisco School of Medicine and UCSF Benioff Children's Hospital, San Francisco, California, USA.ORCID 0000-0002-0146-2499
Pedro A de AlarconPediatrics, University of Illinois College of Medicine Peoria, Peoria, Illinois, USA.

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
Children's Oncology Group Statistics &Data Center GrantU10CA098413 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI DEVIDAS, MEENAKSHI · 2003 to 2013
$67.5M
Chair's CA-180886Chair's U10 CA-98543NCI NIH HHS U10 CA098413NCI NIH HHS U10 CA098543NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899NIH HHSStatistical and Data Center CA-180899Statistical and Data Center U10 CA-98413St. Baldrick's Foundation
6 · The paper itself

Abstract

backgroundOpsoclonus-myoclonus-ataxia syndrome (OMAS) is a rare autoimmune disorder of the nervous system presenting with abnormal eye and limb movements, altered gait, and increased irritability. Two to four percent of children diagnosed with neuroblastoma have neuroblastoma-associated OMAS (NA-OMAS). These children typically present with non-high-risk neuroblastoma that is cured with surgery, with or without chemotherapy. Despite excellent overall survival, patients with NA-OMAS can have significant persistent neurological and developmental issues.

objectiveThis study aimed to describe long-term neurocognitive and adaptive functioning of patients with NA-OMAS treated with multimodal therapy, including intravenous immunoglobulin (IVIG) on Children's Oncology Group (COG) protocol ANBL00P3.

methodsOf 53 children enrolled on ANBL00P3, 25 submitted evaluable neurocognitive data at diagnosis and at least one additional time point within 2 years and were included in the analyses. Adaptive development was assessed via the Vineland Adaptive Behavior Scale, and validated, age-appropriate measures of intellectual function were also administered.

resultsTwenty-one of the 25 patients in this cohort ultimately received IVIG. Descriptive spaghetti plots suggest that this cohort demonstrated stable long-term cognitive functioning and adaptive development over time. This cohort also demonstrated decreased OMAS scores over time consistent with improved OMAS symptoms.

conclusionsWhile statistical significance is limited by small sample size and loss to follow-up over 10 years, findings suggest stable long-term cognitive and adaptive functioning over time in this treated cohort.

Indexed as

NeuroblastomaOpsoclonus-Myoclonus SyndromeAdaptation, PsychologicalAdolescentAntineoplastic Combined Chemotherapy ProtocolsChildChild, PreschoolCognitionCombined Modality TherapyFemaleFollow-Up StudiesHumansImmunoglobulins, IntravenousInfantMalePrognosisImmunoglobulins, IntravenousCOG ANBL00P3long‐term neurocognitive and adaptive functioningneuroblastomaopsoclonus‐myoclonus‐ataxia syndrome (OMAS)opsoclonus‐myoclonus syndrome (OMS)

Identifiers

PMID38689540
PMCPMC11116037

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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.