Evidence map›Paper›PMID 41254957›Full record

ArticlePediatric pulmonology2025

Physical Functioning Report and Pulmonary Function Deficit in Childhood and Adolescent Acute Lymphoblastic Leukemia Survivors: A National Cross-Sectional ALL-STAR Lungs Study.

Sonja Izquierdo Riis Meyer, Mette Tiedemann Skipper, Birgitte Klug Albertsen, Ruta Tuckuviene, Peder Skov Wehner, Thomas Leth Frandsen, Kjeld Schmiegelow, Liv Andrés-Jensen, Kim Gjerum Nielsen, Sune Leisgaard Mørck Rubak

Abstract read
In one paragraph

Article in Pediatric pulmonology, 2025. 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

10 authors.

Sonja Izquierdo Riis MeyerDepartment of Paediatrics and Adolescent Medicine, Danish Centre of Paediatric Pulmonology and Allergology, Aarhus University Hospital, Aarhus, Denmark.ORCID 0000-0003-0144-2196
Mette Tiedemann SkipperDepartment of Clinical Medicine, Aarhus University, Aarhus, Denmark.ORCID 0000-0002-6281-4814
Birgitte Klug AlbertsenDepartment of Clinical Medicine, Aarhus University, Aarhus, Denmark.ORCID 0000-0002-3902-3694
Ruta TuckuvieneDepartment of Paediatrics, Aalborg University Hospital, Aalborg, Denmark.ORCID 0009-0007-2024-0553
Peder Skov WehnerDepartment of Paediatric Haematology and Oncology, H.C. Andersen Children's Hospital, Odense University Hospital, Odense, Denmark.
Thomas Leth FrandsenMary Elizabeth's Hospital - Rigshospitalet for Children, Teens and Expecting Families, Juliane Marie Centre, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.ORCID 0000-0001-8495-5274
Kjeld SchmiegelowDepartment of Paediatrics and Adolescent Medicine, Juliane Marie Centre, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.ORCID 0000-0002-0829-4993
Liv Andrés-JensenDepartment of Paediatrics and Adolescent Medicine, Juliane Marie Centre, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.ORCID 0000-0003-3437-8338
Kim Gjerum NielsenInstitute of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0001-5906-9449
Sune Leisgaard Mørck RubakDepartment of Paediatrics and Adolescent Medicine, Danish Centre of Paediatric Pulmonology and Allergology, Aarhus University Hospital, Aarhus, Denmark.ORCID 0000-0001-7010-2350

Funding

This study has received funding from the Danish Childhood Cancer Foundation (2017-2082, 2019-5966, 2019-5934, 2020-5769, 2020-6737, 2022-8161), The Danish Cancer Society (R192-A11590, R-257-A14720 and R-302-A17277), Riisfort Fonden (grant numbers not applicable (NA)), The Danish Cancer Research Foundation (FID20823), NordForsk (ID 91 172), Ingeniør Otto Christensens Fond (101459), A.P. Møller and Chastine Mc-Kinney Møller Foundation (18-L-0225, L-2022-00042), Skagen Teddy Bear Museum (NA), Childrens' Lung Foundation (NA), Frimodt-Heineke Fonden (NA), Carl og Ellen Hertz's Legat til dansk læge- og naturvidenskab (5-22-2), Fabrikant Einar Willumsens Mindelegat (NA), Frøken Amalie Jørgensens Mindelegat (NA), Anders Hasselbalchs fond til leukæmiens bekæmpelse (NA), Aarhus University Research Foundation (AUFF-F-2024-11-35). The funders were not involved in designing the study, collecting or analyzing data, interpreting results, drafting the manuscript or deciding whether to submit it for publication.
6 · The paper itself

Abstract

backgroundChildhood acute lymphoblastic leukemia (ALL) survivors face an increased risk of pulmonary function deficit (PFD), which may affect physical functioning. We aimed to evaluate parent proxy- and self-reported physical functioning and the association with PFD and abnormal bronchodilator response ( + BDR) among survivors versus controls.

methodsThis cross-sectional study (February 2019-May 2024) included N = 184 ALL survivors (aged 5-17.9 years) from a national NOPHO ALL2008 protocol-treated cohort (eligible, N = 295) ( ≥ 1 year after treatment cessation) and 207 controls. Physical functioning was assessed using the Paediatric Quality of Life Inventory (PedsQL) questionnaire. Pulmonary function tests (PFTs) identified PFD (abnormal PFT) and +BDR according to ERS/ATS criteria. Ordinal logistic regression and t-test compared groups.

resultsALL survivor parents proxy-reported significantly poorer physical functioning than controls (mean difference [MD] -13.3 95% CI [-16.3; -10.3] to MD -10.3 [-17.2; -3.3], p < 0.001 to p = 0.004), but clinically significant impairments were restricted to parent proxy-reports from survivors treated with high-risk (HR) chemotherapy (MD -19.9 [-29.0; -10.7] to -11.5 [-17.5; -5.6], p < 0.001) and stem cell transplantation (HR-SCT) (MD -24.7 [-30.1; -19.4] to -16.9 [-27.4; -6.5], p < 0.001 to p = 0.002) as well as self-reports from HR (MD -11.2 [-18.9; -3.4], p = 0.006) and HR-SCT survivors (MD -14.5 [-24.1; -4.8], p = 0.004). Among 5-15-year-olds, PFD/ + BDR was associated with significantly poorer parent proxy-reported physical functioning in survivors versus controls (MD -14.3 [-21.2; -7.3], p < 0.001). Significant deficits in these groups related to running, engaging in sports/exercise and lifting heavy objects. PFD/ + BDR was not associated with poorer physical functioning reports within survivors (MD -2.5 [-9.0; 3.3] to 0.1 [-13.7; 13.8], p = 0.36-0.99).

conclusionsPhysical functioning in survivors compared to controls varies with intensity of treatment, most evident in HR and HR-SCT survivors, with impairments linked to PFD and +BDR in the youngest. Among survivors, physical functioning did not align with PFD and +BDR status, highlighting the need for parallel assessment of objective and subjective measures during follow-up. Baseline PFT and tailored follow-up are essential for high-risk groups, to detect PFD early and intervene.

Indexed as

Cancer SurvivorsLungPrecursor Cell Lymphoblastic Leukemia-LymphomaAdolescentChildChild, PreschoolCross-Sectional StudiesFemaleHumansMaleQuality of LifeRespiratory Function TestsSelf ReportSurveys and Questionnairesbronchodilator responseleukemia survivorsphysical functioningpulmonary function deficitpulmonary function test in infants/children

Identifiers

PMID41254957
PMCPMC12627931

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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.