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Feasibility of Quantitative Magnetic Resonance Fingerprinting in Ovarian Tumors for T(1) and T(2) Mapping in a PET/MR Setting
Multiparametric magnetic resonance imaging (MRI) can be used to characterize many cancer subtypes including ovarian cancer. Quantitative mapping of MRI relaxation values, such as T(1) and T(2) mapping, is promising for improving tumor assessment beyond conventional qualitative T(1)- and T(2)-weighte...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7025887/ https://www.ncbi.nlm.nih.gov/pubmed/32066996 http://dx.doi.org/10.1109/TRPMS.2019.2905366 |
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author | Kaggie, Joshua D. Deen, Surrin Kessler, Dimitri A. McLean, Mary A. Buonincontri, Guido Schulte, Rolf F. Addley, Helen Sala, Evis Brenton, James Graves, Martin J. Gallagher, Ferdia A. |
author_facet | Kaggie, Joshua D. Deen, Surrin Kessler, Dimitri A. McLean, Mary A. Buonincontri, Guido Schulte, Rolf F. Addley, Helen Sala, Evis Brenton, James Graves, Martin J. Gallagher, Ferdia A. |
author_sort | Kaggie, Joshua D. |
collection | PubMed |
description | Multiparametric magnetic resonance imaging (MRI) can be used to characterize many cancer subtypes including ovarian cancer. Quantitative mapping of MRI relaxation values, such as T(1) and T(2) mapping, is promising for improving tumor assessment beyond conventional qualitative T(1)- and T(2)-weighted images. However, quantitative MRI relaxation mapping methods often involve long scan times due to sequentially measuring many parameters. Magnetic resonance fingerprinting (MRF) is a new method that enables fast quantitative MRI by exploiting the transient signals caused by the variation of pseudorandom sequence parameters. These transient signals are then matched to a simulated dictionary of T(1) and T(2) values to create quantitative maps. The ability of MRF to simultaneously measure multiple parameters, could represent a new approach to characterizing cancer and assessing treatment response. This feasibility study investigates MRF for simultaneous T(1), T(2), and relative proton density (rPD) mapping using ovarian cancer as a model system. |
format | Online Article Text |
id | pubmed-7025887 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
spelling | pubmed-70258872020-02-17 Feasibility of Quantitative Magnetic Resonance Fingerprinting in Ovarian Tumors for T(1) and T(2) Mapping in a PET/MR Setting Kaggie, Joshua D. Deen, Surrin Kessler, Dimitri A. McLean, Mary A. Buonincontri, Guido Schulte, Rolf F. Addley, Helen Sala, Evis Brenton, James Graves, Martin J. Gallagher, Ferdia A. IEEE Trans Radiat Plasma Med Sci Article Multiparametric magnetic resonance imaging (MRI) can be used to characterize many cancer subtypes including ovarian cancer. Quantitative mapping of MRI relaxation values, such as T(1) and T(2) mapping, is promising for improving tumor assessment beyond conventional qualitative T(1)- and T(2)-weighted images. However, quantitative MRI relaxation mapping methods often involve long scan times due to sequentially measuring many parameters. Magnetic resonance fingerprinting (MRF) is a new method that enables fast quantitative MRI by exploiting the transient signals caused by the variation of pseudorandom sequence parameters. These transient signals are then matched to a simulated dictionary of T(1) and T(2) values to create quantitative maps. The ability of MRF to simultaneously measure multiple parameters, could represent a new approach to characterizing cancer and assessing treatment response. This feasibility study investigates MRF for simultaneous T(1), T(2), and relative proton density (rPD) mapping using ovarian cancer as a model system. 2019-03-15 2019-07 /pmc/articles/PMC7025887/ /pubmed/32066996 http://dx.doi.org/10.1109/TRPMS.2019.2905366 Text en http://creativecommons.org/licenses/by/3.0/ This work is licensed under a Creative Commons Attribution 3.0 License. For more information, see http://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Article Kaggie, Joshua D. Deen, Surrin Kessler, Dimitri A. McLean, Mary A. Buonincontri, Guido Schulte, Rolf F. Addley, Helen Sala, Evis Brenton, James Graves, Martin J. Gallagher, Ferdia A. Feasibility of Quantitative Magnetic Resonance Fingerprinting in Ovarian Tumors for T(1) and T(2) Mapping in a PET/MR Setting |
title | Feasibility of Quantitative Magnetic Resonance Fingerprinting in Ovarian Tumors for T(1) and T(2) Mapping in a PET/MR Setting |
title_full | Feasibility of Quantitative Magnetic Resonance Fingerprinting in Ovarian Tumors for T(1) and T(2) Mapping in a PET/MR Setting |
title_fullStr | Feasibility of Quantitative Magnetic Resonance Fingerprinting in Ovarian Tumors for T(1) and T(2) Mapping in a PET/MR Setting |
title_full_unstemmed | Feasibility of Quantitative Magnetic Resonance Fingerprinting in Ovarian Tumors for T(1) and T(2) Mapping in a PET/MR Setting |
title_short | Feasibility of Quantitative Magnetic Resonance Fingerprinting in Ovarian Tumors for T(1) and T(2) Mapping in a PET/MR Setting |
title_sort | feasibility of quantitative magnetic resonance fingerprinting in ovarian tumors for t(1) and t(2) mapping in a pet/mr setting |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7025887/ https://www.ncbi.nlm.nih.gov/pubmed/32066996 http://dx.doi.org/10.1109/TRPMS.2019.2905366 |
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