Evidence map›Paper›PMID 40700618›Full record

Trial reportJournal of the National Cancer Institute2025

Group-based trajectories of health-related quality of life among pediatric patients with high-risk Hodgkin lymphoma.

AnnaLynn M Williams, Angie Mae Rodday, Lindsay A Renfro, Yue Wu, Tara O Henderson, Frank G Keller, Angela Punnett, David Hodgson, Kara M Kelly, Sharon M Castellino and 1 more

Registry-linked trialAbstract readClinical Trial, Phase IIIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Journal of the National Cancer Institute, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02166463 (A Randomized Phase 3 Study of Brentuximab Vedotin), which is not on this 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.

NCT02166463 phase3active not recruitingnot on this map

A Randomized Phase 3 Study of Brentuximab Vedotin (SGN-35) for Newly Diagnosed High-Risk Classical Hodgkin Lymphoma (cHL) in Children and Young Adults

TypeinterventionalSponsorNational Cancer Institute (NCI)Ran2015 to 2026Enrolled600ConditionsAnn Arbor Stage IIB Hodgkin Lymphoma, Ann Arbor Stage IIIB Hodgkin Lymphoma, Ann Arbor Stage IVA Hodgkin Lymphoma, Ann Arbor Stage IVB Hodgkin LymphomaArmsBleomycin Sulfate, Brentuximab Vedotin, Cyclophosphamide, Doxorubicin Hydrochloride, Etoposide
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

11 authors.

AnnaLynn M WilliamsDivision of Supportive Care in Cancer, Department of Surgery, University of Rochester Medical Center, Rochester, NY, United States.ORCID 0000-0002-7042-5851
Angie Mae RoddayInstitute for Clinical Research and Health Policy Studies, Tufts Medical Center, Boston, MA, United States.ORCID 0000-0002-8671-3401
Lindsay A RenfroDivision of Biostatistics, Department of Population and Public Health Sciences, University of Southern California and Children's Oncology Group, Los Angeles, CA, United States.ORCID 0000-0002-4306-1896
Yue WuDepartment of Biostatistics, University of Florida, Gainesville, FL, United States.ORCID 0009-0005-8020-2650
Tara O HendersonDepartment of Pediatrics, University of Chicago Pritzker School of Medicine and Comer Children's Hospital, Chicago, IL, United States.ORCID 0000-0001-9394-6206
Frank G KellerDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA, United States.
Angela PunnettDivision of Hematology-Oncology, Department of Paediatrics, Hospital for Sick Children and University of Toronto, Toronto, ON, Canada.ORCID 0000-0003-4541-0823
David HodgsonDepartment Radiation Oncology, University of Toronto, Toronto, ON, Canada.ORCID 0000-0003-4687-4582
Kara M KellyDepartment of Pediatrics, Roswell Park Comprehensive Cancer Center, University at Buffalo Jacobs School of Medicine and Biomedical Sciences, Buffalo, NY, United States.ORCID 0000-0003-1473-3937
Sharon M CastellinoDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA, United States.ORCID 0000-0001-8367-2002
Susan K ParsonsInstitute for Clinical Research and Health Policy Studies, Tufts Medical Center, Boston, MA, United States.ORCID 0000-0003-0282-6490

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
URCC NCORP Research BaseUG1CA189961 · NCI · UNIVERSITY OF ROCHESTER · PI Michelle C Janelsins, KAREN M. MUSTIAN · 2014 to 2026
$67.7M
Towards a preventive cancer vaccine for children with constitutional mismatch repair deficiencyUG1CA189955 · NCI · PUBLIC HEALTH INSTITUTE · PI BRAD H POLLOCK, Michael E. Roth · 2014 to 2026
$62.5M
Aging-Related Biomarkers of Neurocognitive Function in Long-term Hodgkin Lymphoma SurvivorsR00CA256356 · NCI · UNIVERSITY OF ROCHESTER · PI WILLIAMS, ANNALYNN · 2022 to 2024
$655k
Children's OncologyChildren's Oncology Group U10CA098543Leukemia and Lymphoma SocietyNCI NIH HHS R00 CA256356NCI NIH HHS U10 CA098543NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899NCI NIH HHS UG1 CA189955NCI NIH HHS UG1 CA189961NCORP Grant R00CA256356NCORP Grant UG1CA189955NCTN Operations Center U10CA180886NCTN Statistics and Data Center U10CA180899NIH HHSSt Baldrick's Foundation
6 · The paper itself

Abstract

backgroundHealth-related quality of life (HRQoL) was recently demonstrated to improve throughout therapy for high-risk pediatric Hodgkin lymphoma (HL); however, average scores may not reflect individual differences. This study aimed to identify subgroups of patients with similar HRQoL trajectories from pre- to post-therapy.

methodsAHOD1331 trial participants aged 11-20 (n = 268; mean [SD] age = 15.6 [1.9]; 48% male) completed the Child Health Ratings Inventories-Global scale (HRQoL) prior to treatment, after cycle 2, after cycle 5, and the end of treatment. Group-based trajectory models (GBTMs) identified latent clusters of individuals with similar HRQoL patterns over time. Multivariable multinomial logistic regression estimated the association between a priori defined characteristics and membership in trajectory-based groups. Log-rank tests examined differences in post-T4 progression-free survival (PFS) by trajectory groups.

resultsGBTM identified 3 HRQoL groups: Group 1 (consistently unfavorable [25.7%]), Group 2 (moderate-and-increasing [44.8%]), and Group 3 (consistently favorable [29.5%]). Older age (odds ratio = 1.24, 95% confidence interval = 1.03 to 1.50; P = .022), female sex (2.48, 1.23 to 4.99; P = .011), and Hispanic ethnicity (2.31, 0.97 to 5.50; P = .059) were associated with increased odds of membership in Group 1 vs Group 3. Older age (1.18, 1.00 to 1.39; P = .038) and B-symptoms (2.18, 1.09 to 4.33; P = .027) were associated with increased odds of Group 2 membership vs Group 3. Group membership was not associated with post-T4 PFS.

conclusionsA subgroup of high-risk pediatric HL patients experience persistently poor HRQoL, starting at diagnosis and continuing through therapy. Age, female sex, Hispanic ethnicity, and B-symptoms were linked to worse HRQoL. These findings can help identify patients at higher risk for poor HRQoL and guide intervention. CLINICALTRIALS.GOV: NCT02166463.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsHodgkin DiseaseQuality of LifeAdolescentAge FactorsChildFemaleHumansMaleProgression-Free SurvivalYoung Adult

Identifiers

PMID40700618
PMCPMC12505141

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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.