Cargando…

dAcquisition setting optimization and quantitative imaging for (124)I studies with the Inveon microPET-CT system

BACKGROUND: Noninvasive multimodality imaging is essential for preclinical evaluation of the biodistribution and pharmacokinetics of radionuclide therapy and for monitoring tumor response. Imaging with nonstandard positron-emission tomography [PET] isotopes such as (124)I is promising in that contex...

Descripción completa

Detalles Bibliográficos
Autores principales: Anizan, Nadège, Carlier, Thomas, Hindorf, Cecilia, Barbet, Jacques, Bardiès, Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3311594/
https://www.ncbi.nlm.nih.gov/pubmed/22330760
http://dx.doi.org/10.1186/2191-219X-2-7
_version_ 1782227789225656320
author Anizan, Nadège
Carlier, Thomas
Hindorf, Cecilia
Barbet, Jacques
Bardiès, Manuel
author_facet Anizan, Nadège
Carlier, Thomas
Hindorf, Cecilia
Barbet, Jacques
Bardiès, Manuel
author_sort Anizan, Nadège
collection PubMed
description BACKGROUND: Noninvasive multimodality imaging is essential for preclinical evaluation of the biodistribution and pharmacokinetics of radionuclide therapy and for monitoring tumor response. Imaging with nonstandard positron-emission tomography [PET] isotopes such as (124)I is promising in that context but requires accurate activity quantification. The decay scheme of (124)I implies an optimization of both acquisition settings and correction processing. The PET scanner investigated in this study was the Inveon PET/CT system dedicated to small animal imaging. METHODS: The noise equivalent count rate [NECR], the scatter fraction [SF], and the gamma-prompt fraction [GF] were used to determine the best acquisition parameters for mouse- and rat-sized phantoms filled with (124)I. An image-quality phantom as specified by the National Electrical Manufacturers Association NU 4-2008 protocol was acquired and reconstructed with two-dimensional filtered back projection, 2D ordered-subset expectation maximization [2DOSEM], and 3DOSEM with maximum a posteriori [3DOSEM/MAP] algorithms, with and without attenuation correction, scatter correction, and gamma-prompt correction (weighted uniform distribution subtraction). RESULTS: Optimal energy windows were established for the rat phantom (390 to 550 keV) and the mouse phantom (400 to 590 keV) by combining the NECR, SF, and GF results. The coincidence time window had no significant impact regarding the NECR curve variation. Activity concentration of (124)I measured in the uniform region of an image-quality phantom was underestimated by 9.9% for the 3DOSEM/MAP algorithm with attenuation and scatter corrections, and by 23% with the gamma-prompt correction. Attenuation, scatter, and gamma-prompt corrections decreased the residual signal in the cold insert. CONCLUSIONS: The optimal energy windows were chosen with the NECR, SF, and GF evaluation. Nevertheless, an image quality and an activity quantification assessment were required to establish the most suitable reconstruction algorithm and corrections for (124)I small animal imaging.
format Online
Article
Text
id pubmed-3311594
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Springer
record_format MEDLINE/PubMed
spelling pubmed-33115942012-03-26 dAcquisition setting optimization and quantitative imaging for (124)I studies with the Inveon microPET-CT system Anizan, Nadège Carlier, Thomas Hindorf, Cecilia Barbet, Jacques Bardiès, Manuel EJNMMI Res Original Research BACKGROUND: Noninvasive multimodality imaging is essential for preclinical evaluation of the biodistribution and pharmacokinetics of radionuclide therapy and for monitoring tumor response. Imaging with nonstandard positron-emission tomography [PET] isotopes such as (124)I is promising in that context but requires accurate activity quantification. The decay scheme of (124)I implies an optimization of both acquisition settings and correction processing. The PET scanner investigated in this study was the Inveon PET/CT system dedicated to small animal imaging. METHODS: The noise equivalent count rate [NECR], the scatter fraction [SF], and the gamma-prompt fraction [GF] were used to determine the best acquisition parameters for mouse- and rat-sized phantoms filled with (124)I. An image-quality phantom as specified by the National Electrical Manufacturers Association NU 4-2008 protocol was acquired and reconstructed with two-dimensional filtered back projection, 2D ordered-subset expectation maximization [2DOSEM], and 3DOSEM with maximum a posteriori [3DOSEM/MAP] algorithms, with and without attenuation correction, scatter correction, and gamma-prompt correction (weighted uniform distribution subtraction). RESULTS: Optimal energy windows were established for the rat phantom (390 to 550 keV) and the mouse phantom (400 to 590 keV) by combining the NECR, SF, and GF results. The coincidence time window had no significant impact regarding the NECR curve variation. Activity concentration of (124)I measured in the uniform region of an image-quality phantom was underestimated by 9.9% for the 3DOSEM/MAP algorithm with attenuation and scatter corrections, and by 23% with the gamma-prompt correction. Attenuation, scatter, and gamma-prompt corrections decreased the residual signal in the cold insert. CONCLUSIONS: The optimal energy windows were chosen with the NECR, SF, and GF evaluation. Nevertheless, an image quality and an activity quantification assessment were required to establish the most suitable reconstruction algorithm and corrections for (124)I small animal imaging. Springer 2012-02-13 /pmc/articles/PMC3311594/ /pubmed/22330760 http://dx.doi.org/10.1186/2191-219X-2-7 Text en Copyright ©2012 Anizan et al; licensee Springer. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Anizan, Nadège
Carlier, Thomas
Hindorf, Cecilia
Barbet, Jacques
Bardiès, Manuel
dAcquisition setting optimization and quantitative imaging for (124)I studies with the Inveon microPET-CT system
title dAcquisition setting optimization and quantitative imaging for (124)I studies with the Inveon microPET-CT system
title_full dAcquisition setting optimization and quantitative imaging for (124)I studies with the Inveon microPET-CT system
title_fullStr dAcquisition setting optimization and quantitative imaging for (124)I studies with the Inveon microPET-CT system
title_full_unstemmed dAcquisition setting optimization and quantitative imaging for (124)I studies with the Inveon microPET-CT system
title_short dAcquisition setting optimization and quantitative imaging for (124)I studies with the Inveon microPET-CT system
title_sort dacquisition setting optimization and quantitative imaging for (124)i studies with the inveon micropet-ct system
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3311594/
https://www.ncbi.nlm.nih.gov/pubmed/22330760
http://dx.doi.org/10.1186/2191-219X-2-7
work_keys_str_mv AT anizannadege dacquisitionsettingoptimizationandquantitativeimagingfor124istudieswiththeinveonmicropetctsystem
AT carlierthomas dacquisitionsettingoptimizationandquantitativeimagingfor124istudieswiththeinveonmicropetctsystem
AT hindorfcecilia dacquisitionsettingoptimizationandquantitativeimagingfor124istudieswiththeinveonmicropetctsystem
AT barbetjacques dacquisitionsettingoptimizationandquantitativeimagingfor124istudieswiththeinveonmicropetctsystem
AT bardiesmanuel dacquisitionsettingoptimizationandquantitativeimagingfor124istudieswiththeinveonmicropetctsystem