Evidence map›Paper›PMID 27391297›Full record

ArticleAnnals of the American Thoracic Society2016

Pulmonary Function after Treatment for Childhood Cancer. A Report from the St. Jude Lifetime Cohort Study (SJLIFE).

Daniel M Green, Liang Zhu, Mingjuan Wang, Kirsten K Ness, Matthew J Krasin, Nickhill H Bhakta, M Beth McCarville, Saumini Srinivasan, Dennis C Stokes, DeoKumar Srivastava and 12 more

Abstract read
In one paragraph

Article in Annals of the American Thoracic Society, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
7.8field-weighted citation impact, top 3% of its field
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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. Pooled it
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  5. Observational
  6. Review
  7. Review
  8. Article
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  12. Article
  13. Fine Particulate Matter and Respiratory Healthcare Encounters among Survivors of Childhood Cancers.International journal of environmental research and public health · 2019
    Article
  14. Review
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  16. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 5 institutions in 3 countries.

Daniel M Green1 Department of Epidemiology and Cancer Control.
Liang Zhu3 Department of Biostatistics.
Mingjuan Wang3 Department of Biostatistics.
Kirsten K Ness1 Department of Epidemiology and Cancer Control.
Matthew J Krasin4 Department of Radiation Oncology.
Nickhill H Bhakta2 Department of Oncology.
M Beth McCarville5 Department of Diagnostic Imaging, and.
Saumini Srinivasan7 Department of Pediatrics, University of Tennessee Health Science Center, Memphis, Tennessee; and.
Dennis C Stokes7 Department of Pediatrics, University of Tennessee Health Science Center, Memphis, Tennessee; and.
DeoKumar Srivastava3 Department of Biostatistics.
Rohit Ojha1 Department of Epidemiology and Cancer Control.
Kyla Shelton1 Department of Epidemiology and Cancer Control.
Ching-Hon Pui2 Department of Oncology.
Gregory T Armstrong1 Department of Epidemiology and Cancer Control.
Daniel A Mulrooney1 Department of Epidemiology and Cancer Control.
Monika Metzger2 Department of Oncology.
Sheri L Spunt2 Department of Oncology.
Fariba Navid2 Department of Oncology.
Andrew M Davidoff9 Department of Surgery, St. Jude Children's Research Hospital, Memphis, Tennessee.
Bhaskar N Rao9 Department of Surgery, St. Jude Children's Research Hospital, Memphis, Tennessee.
Leslie L Robison1 Department of Epidemiology and Cancer Control.
Melissa M Hudson1 Department of Epidemiology and Cancer Control.
Institute of Epidemiology, Disease Control and Research · BDSt. Jude Children's Research Hospital · USUniversity of Tennessee Health Science Center · USLaboratory Imaging (Czechia) · CZRadiation Oncology Institute · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 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
NCI NIH HHS P30 CA021765NCI NIH HHS U01 CA195547
6 · The paper itself

Abstract

rationaleThe relationship between treatment-related impairment of pulmonary function in adult survivors of childhood cancer and subsequent physical function has not been studied.

objectivesIn this prospective evaluation of 606 adult survivors of childhood cancer, we sought to determine the risk factors for, as well as the functional impact of, clinically ascertained pulmonary function impairment.

methodsWe measured FEV1, FVC, total lung capacity (TLC), and single-breath diffusing capacity of the lung for carbon monoxide corrected for hemoglobin (DlCOcorr), expressing the results as percent predicted and lower limit of normal (LLN) values, and we also assessed functional exercise capacity (6-minute-walk distance). Lung radiation exposure was expressed as the estimated percentage of lung tissue that received at least 10 Gy (V10). Associations of clinical and treatment factors with pulmonary function measures were assessed using log-binomial regression to calculate relative risks and 95% confidence intervals. MEASUREMENTS AND MAIN

resultsThe participants' median age at evaluation was 34.2 years, and the median elapsed time from diagnosis was 21.9 years. Among the sample population, 50.7% had an FEV1 percent predicted less than 80%, 47.2% had an FVC percent predicted less than 80%, 31.2% had a TLC percent predicted less than 75%, and 44.6% had DlCOcorr percent predicted less than 75%. Also, 49.0% had FEV1 less than the LLN on the basis of the Global Lung Function Initiative (GLI) criteria, and 45.4% had FVC less than LLN. Obstructive lung defects (FEV1/FVC, <0.7) were found in 0.8%, but none had obstructive lung defects on the basis of the GLI criterion of FEV1/FVC less than the LLN. Restrictive lung defects (TLC, <75%) were found in 31.2% of participants. V10 and elapsed time since diagnosis were associated with abnormal FEV1 and FVC based on the National Cancer Institute Common Terminology Criteria for Adverse Events version 4.03 criteria, and with abnormal FEV1 using the GLI criterion. Age at diagnosis was an additional risk factor for abnormal FVC based on the GLI criteria. Age at diagnosis and V10 were associated with abnormal TLC. Increased body mass index, V10, and elapsed time since diagnosis were risk factors for abnormal DlCOcorr. Abnormal pulmonary function tests were associated with decreased 6-minute walk distance.

conclusionsImpaired pulmonary function in adult survivors of childhood cancer is associated with decreased physical function. These patients may benefit from interventions designed to preserve and/or improve pulmonary function.

Indexed as

AdolescentAdultCancer SurvivorsChildChild, PreschoolFemaleForced Expiratory VolumeHumansInfantInfant, NewbornLungMaleMiddle AgedMultivariate AnalysisProspective StudiesRadiation Exposurelung injurymetastasectomyradiation pneumonitisthoracic surgical procedures

Identifiers

PMID27391297
PMCPMC5059496
OpenAlexW2469326909

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.