Evidence map›Paper›PMID 42538814›Full record

ArticleAnnals of the American Thoracic Society2026

Longitudinal Changes in Pulmonary Function After Treatment of Childhood Cancer: A Report from the St. Jude Lifetime Cohort Study.

Neel S Bhatt, Lu Xie, Kendrick Li, DeoKumar Srivastava, Gregory T Armstrong, Andrew M Davidoff, Stephanie B Dixon, Amar Gajjar, I-Chan Huang, Melissa M Hudson and 9 more

Abstract read
In one paragraph

Article in Annals of the American Thoracic Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the 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.

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

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

19 authors.

Neel S BhattClincal Research Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Lu XieDepartment of Biostatistics, St. Jude Children's Research Hospital, Memphis, TN, USA.
Kendrick LiDepartment of Biostatistics, St. Jude Children's Research Hospital, Memphis, TN, USA.
DeoKumar SrivastavaDepartment of Biostatistics, St. Jude Children's Research Hospital, Memphis, TN, USA.
Gregory T ArmstrongDepartment of Epidemiology and Cancer Control, St. Jude Children's Research Hospital, Memphis, TN, USA.
Andrew M DavidoffDepartment of Surgery, St. Jude Children's Research Hospital, Memphis, TN, USA.
Stephanie B DixonDepartment of Epidemiology and Cancer Control, St. Jude Children's Research Hospital, Memphis, TN, USA.
Amar GajjarDepartment of Pediatric Medicine, St. Jude Children's Research Hospital, Memphis, TN, USA.
I-Chan HuangDepartment 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.
Matthew J KrasinDepartment of Radiation Oncology, St. Jude Children's Research Hospital, Memphis, TN, USA.
Mary E Beth McCarvilleDepartment of Radiology, St. Jude Children's Research Hospital, Memphis, TN, USA.
Thomas E MerchantDepartment of Radiation Oncology, St. Jude Children's Research Hospital, Memphis, TN, USA.
Daniel A MulrooneyDepartment of Epidemiology and Cancer Control, 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.
Saumini SrinivasanDepartment of Pediatrics, University of Michigan, Ann Arbor, MI, USA.
Daniel M GreenDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, TN, USA.
Dennis C StokesDepartment of Pediatrics, Vanderbilt University School of Medicine, Nashville, TN, USA.

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI Shondra Michelle Miller · 1985 to 2026
$166.9M
The St. Jude Lifetime CohortU01CA195547 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI HUDSON, MELISSA M, NESS, KIRSTEN KIMBERLIE · 2015 to 2024
$14.9M
The St. Jude Lifetime Cohort StudyU01CA301480 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI MELISSA M HUDSON, Kirsten Kimberlie Ness · 2025 to 2026
$2.1M
NCI NIH HHS P30 CA021765NCI NIH HHS U01 CA195547NCI NIH HHS U01 CA301480
6 · The paper itself

Abstract

RATIONALE/

objectivesData on longitudinal changes in pulmonary function in long-term childhood cancer survivors remain limited. Using a well-characterized cohort of childhood cancer survivors, we analyzed these changes through serial PFT assessments among those exposed to pulmonary-toxic therapy, with available radiation dosimetry data.

methodsIn this single-institutional, hospital-based, retrospective cohort study, Z-scores for FEV1, TLC, and DLCOcorr were calculated, with Z-score ≤-1.65 being considered abnormal. Patient and treatment-related risk-factors for worsening or persistently abnormal Z-scores were assessed. Associations between Z-scores and changes in six-minute walk distance (6MWT), QOL, and persistence or new development of cardiopulmonary and fatigue-related symptoms were studied.

resultsAmong 606 survivors at a median of 27.2 (range 11.3-54.0) years from diagnosis, abnormal FEV1, TLC, and DLCOcorr Z-scores were noted in 49.5%, 51.4%, and 38.0%, respectively. Among those with ≥2 PFT assessments (n = 480), all Z-scores declined, most pronounced at ≥ 30-years from diagnosis. Each 10% increase in lung tissue receiving ≥10 Gy radiation was associated with declining or persistently abnormal FEV1 at 5-years after first PFT (OR 1.18, 95%CI 1.03-1.35). Obesity was associated with declining FEV1 and TLC; Smoking status was associated with declining DLCOcorr Z-scores. Worsening or persistently abnormal Z-scores for FEV1, TLC, and DLCOcorr were associated with decline in 6MWT distance and self-reported physical function. Decline in Z-scores were associated with greater odds of persistent or newly developed shortness of breath with exercise. Decline in DLCOcorr was associated with chronic cough, faintness, and dizziness.

conclusionsPulmonary function declined over time in adult survivors of childhood cancer exposed to pulmonary-toxic therapy, with radiation exposure portending higher risk. Declines were associated with reduced exercise capacity and QOL and increased cardiopulmonary and fatigue-related symptoms. Our findings help identify survivors who may benefit from interventions to preserve pulmonary function.

Indexed as

childhood cancer survivorspulmonary dysfunctionradiation exposure

Identifiers

PMID42538814
PMCPMC13587709

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.