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Examining the Feasibility of Quantifying Receptor Availability Using Cross-Modality Paired-Agent Imaging

PURPOSE: The ability to noninvasively quantify receptor availability (RA) in solid tumors is an aspirational goal of molecular imaging, often challenged by the influence of non-specific accumulation of the contrast agent. Paired-agent imaging (PAI) techniques aim to compensate for this effect by ima...

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Autores principales: Meng, Boyu, Sadeghipour, Negar, Folaron, Margaret R., Strawbridge, Rendall R., Samkoe, Kimberley S., Tichauer, Kenneth M., Davis, Scott C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8760219/
https://www.ncbi.nlm.nih.gov/pubmed/34286423
http://dx.doi.org/10.1007/s11307-021-01629-6
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author Meng, Boyu
Sadeghipour, Negar
Folaron, Margaret R.
Strawbridge, Rendall R.
Samkoe, Kimberley S.
Tichauer, Kenneth M.
Davis, Scott C.
author_facet Meng, Boyu
Sadeghipour, Negar
Folaron, Margaret R.
Strawbridge, Rendall R.
Samkoe, Kimberley S.
Tichauer, Kenneth M.
Davis, Scott C.
author_sort Meng, Boyu
collection PubMed
description PURPOSE: The ability to noninvasively quantify receptor availability (RA) in solid tumors is an aspirational goal of molecular imaging, often challenged by the influence of non-specific accumulation of the contrast agent. Paired-agent imaging (PAI) techniques aim to compensate for this effect by imaging the kinetics of a targeted agent and an untargeted isotype, often simultaneously, and comparing the kinetics of the two agents to estimate RA. This is usually accomplished using two spectrally distinct fluorescent agents, limiting the technique to superficial tissues and/or preclinical applications. Applying the approach in humans using conventional imaging modalities is generally infeasible since most modalities are unable to routinely image multiple agents simultaneously. We examine the ability of PAI to be implemented in a cross-modality paradigm, in which the targeted and untargeted agent kinetics are imaged with different modalities and used to recover receptor availability. PROCEDURES: Eighteen mice bearing orthotopic brain tumors were administered a solution containing three contrast agents: (1) a fluorescent agent targeted to epidermal growth factor receptor (EGFR), (2) an untargeted fluorescent isotype, and (3) a gadolinium-based contrast agent (GBCA) for MRI imaging. The kinetics of all three agents were imaged for 1 h after administration using an MRI-coupled fluorescence tomography system. Paired-agent receptor availability was computed using (1) the conventional all-optical approach using the targeted and untargeted optical agent images and (2) the cross-modality approach using the targeted optical and untargeted MRI-GBCA images. Receptor availability estimates between the two methods were compared. RESULTS: Receptor availability values using the cross-modality approach were highly correlated to the conventional, single-modality approach (r = 0.94; p < 0.00001). CONCLUSION: These results suggest that cross-modality paired-agent imaging for quantifying receptor availability is feasible. Ultimately, cross-modality paired-agent imaging could facilitate rapid, noninvasive receptor availability quantification in humans using hybrid clinical imaging modalities. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11307-021-01629-6.
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spelling pubmed-87602192022-01-26 Examining the Feasibility of Quantifying Receptor Availability Using Cross-Modality Paired-Agent Imaging Meng, Boyu Sadeghipour, Negar Folaron, Margaret R. Strawbridge, Rendall R. Samkoe, Kimberley S. Tichauer, Kenneth M. Davis, Scott C. Mol Imaging Biol Brief Article PURPOSE: The ability to noninvasively quantify receptor availability (RA) in solid tumors is an aspirational goal of molecular imaging, often challenged by the influence of non-specific accumulation of the contrast agent. Paired-agent imaging (PAI) techniques aim to compensate for this effect by imaging the kinetics of a targeted agent and an untargeted isotype, often simultaneously, and comparing the kinetics of the two agents to estimate RA. This is usually accomplished using two spectrally distinct fluorescent agents, limiting the technique to superficial tissues and/or preclinical applications. Applying the approach in humans using conventional imaging modalities is generally infeasible since most modalities are unable to routinely image multiple agents simultaneously. We examine the ability of PAI to be implemented in a cross-modality paradigm, in which the targeted and untargeted agent kinetics are imaged with different modalities and used to recover receptor availability. PROCEDURES: Eighteen mice bearing orthotopic brain tumors were administered a solution containing three contrast agents: (1) a fluorescent agent targeted to epidermal growth factor receptor (EGFR), (2) an untargeted fluorescent isotype, and (3) a gadolinium-based contrast agent (GBCA) for MRI imaging. The kinetics of all three agents were imaged for 1 h after administration using an MRI-coupled fluorescence tomography system. Paired-agent receptor availability was computed using (1) the conventional all-optical approach using the targeted and untargeted optical agent images and (2) the cross-modality approach using the targeted optical and untargeted MRI-GBCA images. Receptor availability estimates between the two methods were compared. RESULTS: Receptor availability values using the cross-modality approach were highly correlated to the conventional, single-modality approach (r = 0.94; p < 0.00001). CONCLUSION: These results suggest that cross-modality paired-agent imaging for quantifying receptor availability is feasible. Ultimately, cross-modality paired-agent imaging could facilitate rapid, noninvasive receptor availability quantification in humans using hybrid clinical imaging modalities. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11307-021-01629-6. Springer International Publishing 2021-07-20 2022 /pmc/articles/PMC8760219/ /pubmed/34286423 http://dx.doi.org/10.1007/s11307-021-01629-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Brief Article
Meng, Boyu
Sadeghipour, Negar
Folaron, Margaret R.
Strawbridge, Rendall R.
Samkoe, Kimberley S.
Tichauer, Kenneth M.
Davis, Scott C.
Examining the Feasibility of Quantifying Receptor Availability Using Cross-Modality Paired-Agent Imaging
title Examining the Feasibility of Quantifying Receptor Availability Using Cross-Modality Paired-Agent Imaging
title_full Examining the Feasibility of Quantifying Receptor Availability Using Cross-Modality Paired-Agent Imaging
title_fullStr Examining the Feasibility of Quantifying Receptor Availability Using Cross-Modality Paired-Agent Imaging
title_full_unstemmed Examining the Feasibility of Quantifying Receptor Availability Using Cross-Modality Paired-Agent Imaging
title_short Examining the Feasibility of Quantifying Receptor Availability Using Cross-Modality Paired-Agent Imaging
title_sort examining the feasibility of quantifying receptor availability using cross-modality paired-agent imaging
topic Brief Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8760219/
https://www.ncbi.nlm.nih.gov/pubmed/34286423
http://dx.doi.org/10.1007/s11307-021-01629-6
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