Evidence map›Paper›PMID 24954547›Full record

Trial reportBiology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation2014

Parametric response mapping as an indicator of bronchiolitis obliterans syndrome after hematopoietic stem cell transplantation.

Craig J Galbán, Jennifer L Boes, Maria Bule, Carrie L Kitko, Daniel R Couriel, Timothy D Johnson, Vihba Lama, Eef D Telenga, Maarten van den Berge, Alnawaz Rehemtulla and 4 more

Abstract readClinical Trial
In one paragraph

Trial report in Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing 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

52 citing papers in PubMed.

  1. Observational
  2. Article
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  6. Review
  7. Article
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  9. Observational
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  11. Article
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  14. Quantitative accuracy of lung function measurement using parametric response mapping: A virtual imaging study.Proceedings of SPIE--the International Society for Optical Engineering · 2024
    Article
  15. Article
  16. Review
  17. Article
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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.

Craig J GalbánDepartment of Radiology, University of Michigan, Ann Arbor, Michigan. Electronic address: cgalban@med.umich.edu.
Jennifer L BoesDepartment of Radiology, University of Michigan, Ann Arbor, Michigan.
Maria BuleDepartment of Radiology, University of Michigan, Ann Arbor, Michigan.
Carrie L KitkoBlood and Marrow Transplant Program, University of Michigan, Ann Arbor, Michigan; Department of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, Michigan.
Daniel R CourielBlood and Marrow Transplant Program, University of Michigan, Ann Arbor, Michigan; Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan.
Timothy D JohnsonDepartment of Biostatistics, University of Michigan, Ann Arbor, Michigan.
Vihba LamaDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan.
Eef D TelengaDepartment of Pulmonary Diseases, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
Maarten van den BergeDepartment of Pulmonary Diseases, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
Alnawaz RehemtullaDepartment of Radiation Oncology, University of Michigan, Ann Arbor, Michigan.
Ella A KazerooniDepartment of Radiology, University of Michigan, Ann Arbor, Michigan.
Michael J PonkowskiBlood and Marrow Transplant Program, University of Michigan, Ann Arbor, Michigan.
Brian D RossDepartment of Radiology, University of Michigan, Ann Arbor, Michigan.
Gregory A YanikBlood and Marrow Transplant Program, University of Michigan, Ann Arbor, Michigan; Department of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, Michigan; Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan.

Funding

QUANTITATION OF HUMAN BRAIN TUMOR THERAPY RESPONSE BY MRP01CA085878 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ROSS, BRIAN D. · 2001 to 2017
$31.9M
Small Animal Imaging CoreP50CA093990 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ROSS, BRIAN D. · 2002 to 2012
$19.0M
Parametric Response Mapping in COPDR01HL122438 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HAN, MEILAN K, MARTINEZ, FERNANDO J · 2014 to 2017
$4.0M
Training Future Imaging Scientists for BiomedicineT32EB005172 · NIBIB · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI FOWLKES, JEFFREY B · 2008 to 2012
$1.1M
NCI NIH HHS P01 CA085878NCI NIH HHS P01CA085878NCI NIH HHS P50 CA093990NCI NIH HHS P50CA93990NHLBI NIH HHS R01 HL122438NIBIB NIH HHS T32 EB005172NIBIB NIH HHS T32EB005172
6 · The paper itself

Abstract

The management of bronchiolitis obliterans syndrome (BOS) after hematopoietic cell transplantation presents many challenges, both diagnostically and therapeutically. We developed a computed tomography (CT) voxel-wise methodology termed parametric response mapping (PRM) that quantifies normal parenchyma, functional small airway disease (PRM(fSAD)), emphysema, and parenchymal disease as relative lung volumes. We now investigate the use of PRM as an imaging biomarker in the diagnosis of BOS. PRM was applied to CT data from 4 patient cohorts: acute infection (n = 11), BOS at onset (n = 34), BOS plus infection (n = 9), and age-matched, nontransplant control subjects (n = 23). Pulmonary function tests and bronchoalveolar lavage were used for group classification. Mean values for PRM(fSAD) were significantly greater in patients with BOS (38% ± 2%) when compared with those with infection alone (17% ± 4%, P < .0001) and age-matched control subjects (8.4% ± 1%, P < .0001). Patients with BOS had similar PRM(fSAD) profiles, whether a concurrent infection was present or not. An optimal cut-point for PRM(fSAD) of 28% of the total lung volume was identified, with values >28% highly indicative of BOS occurrence. PRM may provide a major advance in our ability to identify the small airway obstruction that characterizes BOS, even in the presence of concurrent infection.

Indexed as

Hematopoietic Stem Cell TransplantationAdolescentAdultAgedBronchiolitis ObliteransBronchoalveolar Lavage FluidCase-Control StudiesChildFemaleHematologic NeoplasmsHumansLungMaleMiddle AgedMyeloablative AgonistsProspective StudiesMyeloablative AgonistsBronchiolitis obliterans syndromePulmonaryTransplantation

Identifiers

PMID24954547
PMCPMC4163140

What OpenQuestion holds

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Registered trials

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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.