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Diffusion MRI and Novel Texture Analysis in Osteosarcoma Xenotransplants Predicts Response to Anti-Checkpoint Therapy

Combinations of targeted drugs have been employed to treat sarcomas, however, response rates have not improved notably, therefore emphasizing the need for novel treatments. In addition, imaging approaches to assess therapeutic response is lacking, as currently measurable indices, such as volume and/...

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Autores principales: Foroutan, Parastou, Kreahling, Jenny M., Morse, David L., Grove, Olya, Lloyd, Mark C., Reed, Damon, Raghavan, Meera, Altiok, Soner, Martinez, Gary V., Gillies, Robert J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3865096/
https://www.ncbi.nlm.nih.gov/pubmed/24358232
http://dx.doi.org/10.1371/journal.pone.0082875
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author Foroutan, Parastou
Kreahling, Jenny M.
Morse, David L.
Grove, Olya
Lloyd, Mark C.
Reed, Damon
Raghavan, Meera
Altiok, Soner
Martinez, Gary V.
Gillies, Robert J.
author_facet Foroutan, Parastou
Kreahling, Jenny M.
Morse, David L.
Grove, Olya
Lloyd, Mark C.
Reed, Damon
Raghavan, Meera
Altiok, Soner
Martinez, Gary V.
Gillies, Robert J.
author_sort Foroutan, Parastou
collection PubMed
description Combinations of targeted drugs have been employed to treat sarcomas, however, response rates have not improved notably, therefore emphasizing the need for novel treatments. In addition, imaging approaches to assess therapeutic response is lacking, as currently measurable indices, such as volume and/or diameter, do not accurately correlate with changes in tumor biology. In this study, quantitative and profound analyses of magnetic resonance imaging (MRI) were developed to evaluate these as imaging biomarkers for MK1775 and Gem in an osteosarcoma xenotransplant model at early time-points following treatment. Notably, we showed that Gem and Gem+MK1775 groups had significantly inhibited tumor growth by day 4, which was presaged by elevations in mean ADC by 24 hours post treatment. Significant differences were also observed at later time points for the Gem+MK1775 combination and MK1775 therapy. ADC distribution and entropy (randomness of ADC values) were also elevated by 24 hours following therapy. Immunohistochemistry demonstrated that these treatment-related increases in ADC correlated with apoptosis and observed cell condensations (dense- and exploded bodies). These findings underline the role of ADC as a quantitative imaging biomarker for therapy-induced response and show promising clinical relevance in the sarcoma patient population.
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spelling pubmed-38650962013-12-19 Diffusion MRI and Novel Texture Analysis in Osteosarcoma Xenotransplants Predicts Response to Anti-Checkpoint Therapy Foroutan, Parastou Kreahling, Jenny M. Morse, David L. Grove, Olya Lloyd, Mark C. Reed, Damon Raghavan, Meera Altiok, Soner Martinez, Gary V. Gillies, Robert J. PLoS One Research Article Combinations of targeted drugs have been employed to treat sarcomas, however, response rates have not improved notably, therefore emphasizing the need for novel treatments. In addition, imaging approaches to assess therapeutic response is lacking, as currently measurable indices, such as volume and/or diameter, do not accurately correlate with changes in tumor biology. In this study, quantitative and profound analyses of magnetic resonance imaging (MRI) were developed to evaluate these as imaging biomarkers for MK1775 and Gem in an osteosarcoma xenotransplant model at early time-points following treatment. Notably, we showed that Gem and Gem+MK1775 groups had significantly inhibited tumor growth by day 4, which was presaged by elevations in mean ADC by 24 hours post treatment. Significant differences were also observed at later time points for the Gem+MK1775 combination and MK1775 therapy. ADC distribution and entropy (randomness of ADC values) were also elevated by 24 hours following therapy. Immunohistochemistry demonstrated that these treatment-related increases in ADC correlated with apoptosis and observed cell condensations (dense- and exploded bodies). These findings underline the role of ADC as a quantitative imaging biomarker for therapy-induced response and show promising clinical relevance in the sarcoma patient population. Public Library of Science 2013-12-16 /pmc/articles/PMC3865096/ /pubmed/24358232 http://dx.doi.org/10.1371/journal.pone.0082875 Text en © 2013 Foroutan 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Foroutan, Parastou
Kreahling, Jenny M.
Morse, David L.
Grove, Olya
Lloyd, Mark C.
Reed, Damon
Raghavan, Meera
Altiok, Soner
Martinez, Gary V.
Gillies, Robert J.
Diffusion MRI and Novel Texture Analysis in Osteosarcoma Xenotransplants Predicts Response to Anti-Checkpoint Therapy
title Diffusion MRI and Novel Texture Analysis in Osteosarcoma Xenotransplants Predicts Response to Anti-Checkpoint Therapy
title_full Diffusion MRI and Novel Texture Analysis in Osteosarcoma Xenotransplants Predicts Response to Anti-Checkpoint Therapy
title_fullStr Diffusion MRI and Novel Texture Analysis in Osteosarcoma Xenotransplants Predicts Response to Anti-Checkpoint Therapy
title_full_unstemmed Diffusion MRI and Novel Texture Analysis in Osteosarcoma Xenotransplants Predicts Response to Anti-Checkpoint Therapy
title_short Diffusion MRI and Novel Texture Analysis in Osteosarcoma Xenotransplants Predicts Response to Anti-Checkpoint Therapy
title_sort diffusion mri and novel texture analysis in osteosarcoma xenotransplants predicts response to anti-checkpoint therapy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3865096/
https://www.ncbi.nlm.nih.gov/pubmed/24358232
http://dx.doi.org/10.1371/journal.pone.0082875
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