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(18)F-FDG PET/CT-based early treatment response evaluation of nanoparticle-assisted photothermal cancer therapy

Within the field of nanoparticle-assisted photothermal cancer therapy, focus has mostly been on developing novel heat-generating nanoparticles with the right optical and dimensional properties. Comparison and evaluation of their performance in tumor-bearing animals are commonly assessed by changes i...

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Autores principales: Norregaard, Kamilla, Jørgensen, Jesper T., Simón, Marina, Melander, Fredrik, Kristensen, Lotte K., Bendix, Pól M., Andresen, Thomas L., Oddershede, Lene B., Kjaer, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5443528/
https://www.ncbi.nlm.nih.gov/pubmed/28542311
http://dx.doi.org/10.1371/journal.pone.0177997
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author Norregaard, Kamilla
Jørgensen, Jesper T.
Simón, Marina
Melander, Fredrik
Kristensen, Lotte K.
Bendix, Pól M.
Andresen, Thomas L.
Oddershede, Lene B.
Kjaer, Andreas
author_facet Norregaard, Kamilla
Jørgensen, Jesper T.
Simón, Marina
Melander, Fredrik
Kristensen, Lotte K.
Bendix, Pól M.
Andresen, Thomas L.
Oddershede, Lene B.
Kjaer, Andreas
author_sort Norregaard, Kamilla
collection PubMed
description Within the field of nanoparticle-assisted photothermal cancer therapy, focus has mostly been on developing novel heat-generating nanoparticles with the right optical and dimensional properties. Comparison and evaluation of their performance in tumor-bearing animals are commonly assessed by changes in tumor volume; however, this is usually a late-occurring event. This study implements 2-deoxy-2-[F-18]fluoro-D-glucose positron emission tomography imaging to perform early evaluation of the treatment outcome of photothermal therapy. Silica-gold nanoshells (NS) are administered intravenously to nude mice bearing human neuroendocrine tumor xenografts and the tumors are irradiated by a near-infrared laser. The animals are positron emission tomography scanned with 2-deoxy-2-[F-18]fluoro-D-glucose one day before and one day after treatment. Using this setup, a significant decrease in tumor uptake of 2-deoxy-2-[F-18]fluoro-D-glucose is found already one day after therapy in the group receiving NS and laser treatment compared to control animals. At this time point no change in tumor volume can be detected. Moreover, the change in tumor uptake, is used to stratify the animals into responders and non-responders, where the responding group matched improved survival. Overall, these findings support the use of 2-deoxy-2-[F-18]fluoro-D-glucose positron emission tomography imaging for preclinical and clinical evaluation and optimization of photothermal therapy.
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spelling pubmed-54435282017-06-06 (18)F-FDG PET/CT-based early treatment response evaluation of nanoparticle-assisted photothermal cancer therapy Norregaard, Kamilla Jørgensen, Jesper T. Simón, Marina Melander, Fredrik Kristensen, Lotte K. Bendix, Pól M. Andresen, Thomas L. Oddershede, Lene B. Kjaer, Andreas PLoS One Research Article Within the field of nanoparticle-assisted photothermal cancer therapy, focus has mostly been on developing novel heat-generating nanoparticles with the right optical and dimensional properties. Comparison and evaluation of their performance in tumor-bearing animals are commonly assessed by changes in tumor volume; however, this is usually a late-occurring event. This study implements 2-deoxy-2-[F-18]fluoro-D-glucose positron emission tomography imaging to perform early evaluation of the treatment outcome of photothermal therapy. Silica-gold nanoshells (NS) are administered intravenously to nude mice bearing human neuroendocrine tumor xenografts and the tumors are irradiated by a near-infrared laser. The animals are positron emission tomography scanned with 2-deoxy-2-[F-18]fluoro-D-glucose one day before and one day after treatment. Using this setup, a significant decrease in tumor uptake of 2-deoxy-2-[F-18]fluoro-D-glucose is found already one day after therapy in the group receiving NS and laser treatment compared to control animals. At this time point no change in tumor volume can be detected. Moreover, the change in tumor uptake, is used to stratify the animals into responders and non-responders, where the responding group matched improved survival. Overall, these findings support the use of 2-deoxy-2-[F-18]fluoro-D-glucose positron emission tomography imaging for preclinical and clinical evaluation and optimization of photothermal therapy. Public Library of Science 2017-05-24 /pmc/articles/PMC5443528/ /pubmed/28542311 http://dx.doi.org/10.1371/journal.pone.0177997 Text en © 2017 Norregaard et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Norregaard, Kamilla
Jørgensen, Jesper T.
Simón, Marina
Melander, Fredrik
Kristensen, Lotte K.
Bendix, Pól M.
Andresen, Thomas L.
Oddershede, Lene B.
Kjaer, Andreas
(18)F-FDG PET/CT-based early treatment response evaluation of nanoparticle-assisted photothermal cancer therapy
title (18)F-FDG PET/CT-based early treatment response evaluation of nanoparticle-assisted photothermal cancer therapy
title_full (18)F-FDG PET/CT-based early treatment response evaluation of nanoparticle-assisted photothermal cancer therapy
title_fullStr (18)F-FDG PET/CT-based early treatment response evaluation of nanoparticle-assisted photothermal cancer therapy
title_full_unstemmed (18)F-FDG PET/CT-based early treatment response evaluation of nanoparticle-assisted photothermal cancer therapy
title_short (18)F-FDG PET/CT-based early treatment response evaluation of nanoparticle-assisted photothermal cancer therapy
title_sort (18)f-fdg pet/ct-based early treatment response evaluation of nanoparticle-assisted photothermal cancer therapy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5443528/
https://www.ncbi.nlm.nih.gov/pubmed/28542311
http://dx.doi.org/10.1371/journal.pone.0177997
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