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Development of a Multiparametric Voxel-Based Magnetic Resonance Imaging Biomarker for Early Cancer Therapeutic Response Assessment
Quantitative magnetic resonance imaging (MRI)-based biomarkers, which capture physiological and functional tumor processes, were evaluated as imaging surrogates of early tumor response following chemoradiotherapy in glioma patients. A multiparametric extension of a voxel-based analysis, referred as...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Grapho Publications, LLC
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4643274/ https://www.ncbi.nlm.nih.gov/pubmed/26568982 http://dx.doi.org/10.18383/j.tom.2015.00124 |
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author | Galbán, Craig J. Lemasson, Benjamin Hoff, Benjamin A. Johnson, Timothy D. Sundgren, Pia C. Tsien, Christina Chenevert, Thomas L. Ross, Brian D. |
author_facet | Galbán, Craig J. Lemasson, Benjamin Hoff, Benjamin A. Johnson, Timothy D. Sundgren, Pia C. Tsien, Christina Chenevert, Thomas L. Ross, Brian D. |
author_sort | Galbán, Craig J. |
collection | PubMed |
description | Quantitative magnetic resonance imaging (MRI)-based biomarkers, which capture physiological and functional tumor processes, were evaluated as imaging surrogates of early tumor response following chemoradiotherapy in glioma patients. A multiparametric extension of a voxel-based analysis, referred as the parametric response map (PRM), was applied to quantitative MRI maps to test the predictive potential of this metric for detecting response. Fifty-six subjects with newly diagnosed high-grade gliomas treated with radiation and concurrent temozolomide were enrolled in a single-site prospective institutional review board-approved MRI study. Apparent diffusion coefficient (ADC) and relative cerebral blood volume (rCBV) maps were acquired before therapy and 3 weeks after therapy was initiated. Multiparametric PRM (mPRM) was applied to both physiological MRI maps and evaluated as an imaging biomarker of patient survival. For comparison, single-biomarker PRMs were also evaluated in this study. The simultaneous analysis of ADC and rCBV by the mPRM approach was found to improve the predictive potential for patient survival over single PRM measures. With an array of quantitative imaging parameters being evaluated as biomarkers of therapeutic response, mPRM shows promise as a new methodology for consolidating physiologically distinct imaging parameters into a single interpretable and quantitative metric. |
format | Online Article Text |
id | pubmed-4643274 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Grapho Publications, LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-46432742015-11-13 Development of a Multiparametric Voxel-Based Magnetic Resonance Imaging Biomarker for Early Cancer Therapeutic Response Assessment Galbán, Craig J. Lemasson, Benjamin Hoff, Benjamin A. Johnson, Timothy D. Sundgren, Pia C. Tsien, Christina Chenevert, Thomas L. Ross, Brian D. Tomography Research Article Quantitative magnetic resonance imaging (MRI)-based biomarkers, which capture physiological and functional tumor processes, were evaluated as imaging surrogates of early tumor response following chemoradiotherapy in glioma patients. A multiparametric extension of a voxel-based analysis, referred as the parametric response map (PRM), was applied to quantitative MRI maps to test the predictive potential of this metric for detecting response. Fifty-six subjects with newly diagnosed high-grade gliomas treated with radiation and concurrent temozolomide were enrolled in a single-site prospective institutional review board-approved MRI study. Apparent diffusion coefficient (ADC) and relative cerebral blood volume (rCBV) maps were acquired before therapy and 3 weeks after therapy was initiated. Multiparametric PRM (mPRM) was applied to both physiological MRI maps and evaluated as an imaging biomarker of patient survival. For comparison, single-biomarker PRMs were also evaluated in this study. The simultaneous analysis of ADC and rCBV by the mPRM approach was found to improve the predictive potential for patient survival over single PRM measures. With an array of quantitative imaging parameters being evaluated as biomarkers of therapeutic response, mPRM shows promise as a new methodology for consolidating physiologically distinct imaging parameters into a single interpretable and quantitative metric. Grapho Publications, LLC 2015-09 /pmc/articles/PMC4643274/ /pubmed/26568982 http://dx.doi.org/10.18383/j.tom.2015.00124 Text en © 2015 The Authors. Published by Grapho Publications, LLC http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Research Article Galbán, Craig J. Lemasson, Benjamin Hoff, Benjamin A. Johnson, Timothy D. Sundgren, Pia C. Tsien, Christina Chenevert, Thomas L. Ross, Brian D. Development of a Multiparametric Voxel-Based Magnetic Resonance Imaging Biomarker for Early Cancer Therapeutic Response Assessment |
title | Development of a Multiparametric Voxel-Based Magnetic Resonance Imaging Biomarker for Early Cancer Therapeutic Response Assessment |
title_full | Development of a Multiparametric Voxel-Based Magnetic Resonance Imaging Biomarker for Early Cancer Therapeutic Response Assessment |
title_fullStr | Development of a Multiparametric Voxel-Based Magnetic Resonance Imaging Biomarker for Early Cancer Therapeutic Response Assessment |
title_full_unstemmed | Development of a Multiparametric Voxel-Based Magnetic Resonance Imaging Biomarker for Early Cancer Therapeutic Response Assessment |
title_short | Development of a Multiparametric Voxel-Based Magnetic Resonance Imaging Biomarker for Early Cancer Therapeutic Response Assessment |
title_sort | development of a multiparametric voxel-based magnetic resonance imaging biomarker for early cancer therapeutic response assessment |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4643274/ https://www.ncbi.nlm.nih.gov/pubmed/26568982 http://dx.doi.org/10.18383/j.tom.2015.00124 |
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