Pauline T. Lukey
Clinical quantification of the integrin αvβ6 by [18F]FB-A20FMDV2 positron emission tomography in healthy and fibrotic human lung (PETAL Study)
Lukey, Pauline T.; Coello, Christopher; Gunn, Roger; Parker, Christine; Wilson, Frederick J.; Saleem, Azeem; Garman, Nadia; Costa, Maria; Kendrick, Stuart; Onega, Mayca; Kang’ombe, Arthur R.; Listanco, Allan; Davies, James; Ramada-Magalhaes, Joaquim; Moz, Sara; Fahy, William A.; Maher, Toby M.; Jenkins, Gisli; Passchier, Jan; Marshall, Richard P.
Authors
Christopher Coello
Roger Gunn
Christine Parker
Frederick J. Wilson
Dr Azeem Saleem A.Saleem@hull.ac.uk
Reader and Honorary Consultant in Clinical Oncology
Nadia Garman
Maria Costa
Stuart Kendrick
Mayca Onega
Arthur R. Kang’ombe
Allan Listanco
James Davies
Joaquim Ramada-Magalhaes
Sara Moz
William A. Fahy
Toby M. Maher
Gisli Jenkins
Jan Passchier
Richard P. Marshall
Abstract
© 2019, The Author(s). Purpose: The RGD-integrin, αvβ6, plays a role in the pathogenesis of pulmonary fibrosis through activation of transforming growth factor beta (TGFβ). This study sought to quantify expression of αvβ6 in the lungs of healthy humans and subjects with pulmonary fibrosis using the αvβ6-selective [18F]FB-A20FMDV2 PET ligand. Methods: [18F]FB-A20FMDV2 PET/CT scans were performed in healthy subjects and those with fibrotic lung disease. Standard uptake values (SUV) and volume of distribution (VT) were used to quantify αvβ6 expression. In subjects with fibrotic lung disease, qualitative assessment of the relationship between αvβ6 expression and the distribution of fibrosis on high resolution computed tomography was conducted. Results: A total of 15 participants (6 healthy, 7 with idiopathic pulmonary fibrosis (IPF) and 2 with connective tissue disease (CTD) associated PF) were enrolled. VT and SUV of [18F]FB-A20FMDV2 were increased in the lungs of subjects with pulmonary fibrosis (PF) compared with healthy subjects. Geometric mean VT (95% CI) was 0.88 (0.60, 1.29) mL/cm3 for healthy subjects, and 1.40 (1.22, 1.61) mL/cm3 for subjects with IPF; and SUV was 0.54 (0.36, 0.81) g/mL for healthy subjects and 1.03 (0.86, 1.22) g/mL for subjects with IPF. The IPF/healthy VT ratio (geometric mean, (95% CI of ratio)) was 1.59 (1.09, 2.32) (probability ratio > 1 = 0.988)) and the SUV ratio was 1.91 (1.27, 2.87) (probability ratio > 1 = 0.996). Increased uptake of [18F]FB-A20FMDV2 in PF was predominantly confined to fibrotic areas. [18F]FB-A20FMDV2 measurements were reproducible at an interval of 2 weeks. [18F]FB-A20FMDV2 was safe and well tolerated. Conclusions: Lung uptake of [18F]FB-A20FMDV2, a measure of expression of the integrin αvβ6, was markedly increased in subjects with PF compared with healthy subjects.
Citation
Lukey, P. T., Coello, C., Gunn, R., Parker, C., Wilson, F. J., Saleem, A., Garman, N., Costa, M., Kendrick, S., Onega, M., Kang’ombe, A. R., Listanco, A., Davies, J., Ramada-Magalhaes, J., Moz, S., Fahy, W. A., Maher, T. M., Jenkins, G., Passchier, J., & Marshall, R. P. (2020). Clinical quantification of the integrin αvβ6 by [18F]FB-A20FMDV2 positron emission tomography in healthy and fibrotic human lung (PETAL Study). European journal of nuclear medicine and molecular imaging, 47(4), 967-979. https://doi.org/10.1007/s00259-019-04586-z
Journal Article Type | Article |
---|---|
Acceptance Date | Oct 16, 2019 |
Online Publication Date | Dec 9, 2019 |
Publication Date | 2020-04 |
Deposit Date | Feb 10, 2021 |
Publicly Available Date | Feb 11, 2021 |
Journal | European Journal of Nuclear Medicine and Molecular Imaging |
Print ISSN | 1619-7070 |
Publisher | Springer Verlag |
Peer Reviewed | Peer Reviewed |
Volume | 47 |
Issue | 4 |
Pages | 967-979 |
DOI | https://doi.org/10.1007/s00259-019-04586-z |
Keywords | Idiopathic pulmonary fibrosis; [18F]FB-A20FMDV2 PET/CT; αvβ6 integrin; Biomarker; Pulmonary fibrosis; PET; Clinical study |
Public URL | https://hull-repository.worktribe.com/output/3630026 |
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Copyright Statement
© The Author(s) 2019. Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
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