Evidence map›Paper›PMID 38941494›Full record

ArticleJournal of the National Cancer Institute2024

Using neurocognitive phenotypes to inform interventions for adult survivors of childhood cancer.

Pia Banerjee, Nicholas S Phillips, Wei Liu, Matthew J Ehrhardt, Nickhill Bhakta, Tara M Brinkman, Annalynn M Williams, Yutaka Yasui, Raja B Khan, Deokumar Srivastava and 4 more

Abstract read
In one paragraph

Article in Journal of the National Cancer Institute, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

14 authors.

Pia BanerjeeDepartment of Epidemiology and Cancer Control, St Jude Children's Research Hospital, Memphis, TN, USA.
Nicholas S PhillipsDepartment of Psychology and Biobehavioral Science, St Jude Children's Research Hospital, Memphis, TN, USA.ORCID 0000-0002-2021-4036
Wei LiuDepartment of Biostatistics, St Jude Children's Research Hospital, Memphis, TN, USA.
Matthew J EhrhardtDepartment of Epidemiology and Cancer Control, St Jude Children's Research Hospital, Memphis, TN, USA.
Nickhill BhaktaDepartment of Epidemiology and Cancer Control, St Jude Children's Research Hospital, Memphis, TN, USA.
Tara M BrinkmanDepartment of Epidemiology and Cancer Control, St Jude Children's Research Hospital, Memphis, TN, USA.
Annalynn M WilliamsDepartment of Epidemiology and Cancer Control, St Jude Children's Research Hospital, Memphis, TN, USA.
Yutaka YasuiDepartment of Epidemiology and Cancer Control, St Jude Children's Research Hospital, Memphis, TN, USA.ORCID 0000-0002-7717-8638
Raja B KhanDepartment of Pediatric Medicine, Division of Neurology, St Jude Children's Research Hospital, Memphis, TN, USA.
Deokumar SrivastavaDepartment of Biostatistics, St Jude Children's Research Hospital, Memphis, TN, USA.
Kirsten K NessDepartment of Epidemiology and Cancer Control, St Jude Children's Research Hospital, Memphis, TN, USA.
Leslie L RobisonDepartment of Epidemiology and Cancer Control, St Jude Children's Research Hospital, Memphis, TN, USA.
Melissa M HudsonDepartment of Epidemiology and Cancer Control, St Jude Children's Research Hospital, Memphis, TN, USA.
Kevin R KrullDepartment of Psychology and Biobehavioral Science, St Jude Children's Research Hospital, Memphis, TN, USA.

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
URCC NCORP Research BaseUG1CA189961 · NCI · UNIVERSITY OF ROCHESTER · PI Michelle C Janelsins, KAREN M. MUSTIAN · 2014 to 2026
$67.7M
The St. Jude Lifetime CohortU01CA195547 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI HUDSON, MELISSA M, NESS, KIRSTEN KIMBERLIE · 2015 to 2024
$14.9M
Training in Pediatric Cancer Survivorship Outcomes and InterventionsT32CA225590 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI Kevin R Krull · 2018 to 2026
$2.4M
American Lebanese-Syrian Associated CharitiesNational Institute of HealthNCI NIH HHS CA195547NCI NIH HHS P30 CA021765NCI NIH HHS U01 CA195547NCI NIH HHS UG1 CA189961
6 · The paper itself

Abstract

backgroundNeurocognitive impairments are sequelae of childhood cancer treatment, however little guidance is given to clinicians on common phenotypes of impairment or modifiable risk factors that could lead to personalized interventions in survivorship.

methodsStandardized clinical testing of neurocognitive function was conducted in 2958 (74.1%) eligible survivors, who were at least 5 years postdiagnosis and aged older than 18 years, and 477 community controls. Impairment was examined across 20 measures, and phenotypes were determined by latent class analysis. Multinomial logistic regression was used to estimate risk for phenotype, predicted by cancer diagnosis and treatment exposures, chronic health conditions, and lifestyle, adjusted for sex and age. Associations between phenotypes and social attainment were examined.

resultsFive neurocognitive phenotypes were identified in survivors (global impairment 3.7%, impaired attention 5.0%, memory impairment 7.2%, processing speed and executive function impairment 9.3%, no impairment 74.8%). Risk of global impairment was associated with severe chronic health condition burden (odds ratio [OR] = 20.17, 95% confidence interval [CI] = 11.41 to 35.63) including cerebrovascular disease (OR = 14.5, 95% CI = 5.47 to 38.44) and cerebrovascular accident (OR = 14.7, 95% CI = 7.50 to 26.40). Modifiable risk factors, such as quitting smoking, reduced risk for global impairment (OR = 0.21, 95% CI = 0.06 to 0.66). Low physical activity increased risk for global impairment (OR = 4.54, 95% CI = 2.86 to 7.21), attention impairment (OR = 2.01, 95% CI = 1.41 to 2.87), processing speed and executive function impairment (OR = 1.90, 95% CI = 1.46 to 2.48), and memory impairment (OR = 2.09, 95% CI = 1.54 to 2.82).

conclusionsResults support the clinical utility of neurocognitive phenotyping to develop risk profiles and personalized clinical interventions, such as preventing cerebrovascular disease in anthracycline-treated survivors by preventing hypercholesterolemia, smoking, and sedentary lifestyle, to reduce the risk for global impairment.

Indexed as

Cancer SurvivorsNeoplasmsPhenotypeAdolescentAdultChildCognitive DysfunctionFemaleHumansMaleMiddle AgedNeurocognitive DisordersNeuropsychological TestsRisk FactorsYoung Adult

Identifiers

PMID38941494
PMCPMC11542983

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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.