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Hyperpolarized (13)C MRI of Tumor Metabolism Demonstrates Early Metabolic Response to Neoadjuvant Chemotherapy in Breast Cancer

PURPOSE: To compare hyperpolarized carbon 13 ((13)C) MRI with dynamic contrast material–enhanced (DCE) MRI in the detection of early treatment response in breast cancer. MATERIALS AND METHODS: In this institutional review board–approved prospective study, a woman with triple-negative breast cancer (...

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Autores principales: Woitek, Ramona, McLean, Mary A., Gill, Andrew B., Grist, James T., Provenzano, Elena, Patterson, Andrew J., Ursprung, Stephan, Torheim, Turid, Zaccagna, Fulvio, Locke, Matthew, Laurent, Marie-Christine, Hilborne, Sarah, Frary, Amy, Beer, Lucian, Rundo, Leonardo, Patterson, Ilse, Slough, Rhys, Kane, Justine, Biggs, Heather, Harrison, Emma, Lanz, Titus, Basu, Bristi, Baird, Richard, Sala, Evis, Graves, Martin J., Gilbert, Fiona J., Abraham, Jean E., Caldas, Carlos, Brindle, Kevin M., Gallagher, Ferdia A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Radiological Society of North America 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7398116/
https://www.ncbi.nlm.nih.gov/pubmed/32803167
http://dx.doi.org/10.1148/rycan.2020200017
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author Woitek, Ramona
McLean, Mary A.
Gill, Andrew B.
Grist, James T.
Provenzano, Elena
Patterson, Andrew J.
Ursprung, Stephan
Torheim, Turid
Zaccagna, Fulvio
Locke, Matthew
Laurent, Marie-Christine
Hilborne, Sarah
Frary, Amy
Beer, Lucian
Rundo, Leonardo
Patterson, Ilse
Slough, Rhys
Kane, Justine
Biggs, Heather
Harrison, Emma
Lanz, Titus
Basu, Bristi
Baird, Richard
Sala, Evis
Graves, Martin J.
Gilbert, Fiona J.
Abraham, Jean E.
Caldas, Carlos
Brindle, Kevin M.
Gallagher, Ferdia A.
author_facet Woitek, Ramona
McLean, Mary A.
Gill, Andrew B.
Grist, James T.
Provenzano, Elena
Patterson, Andrew J.
Ursprung, Stephan
Torheim, Turid
Zaccagna, Fulvio
Locke, Matthew
Laurent, Marie-Christine
Hilborne, Sarah
Frary, Amy
Beer, Lucian
Rundo, Leonardo
Patterson, Ilse
Slough, Rhys
Kane, Justine
Biggs, Heather
Harrison, Emma
Lanz, Titus
Basu, Bristi
Baird, Richard
Sala, Evis
Graves, Martin J.
Gilbert, Fiona J.
Abraham, Jean E.
Caldas, Carlos
Brindle, Kevin M.
Gallagher, Ferdia A.
author_sort Woitek, Ramona
collection PubMed
description PURPOSE: To compare hyperpolarized carbon 13 ((13)C) MRI with dynamic contrast material–enhanced (DCE) MRI in the detection of early treatment response in breast cancer. MATERIALS AND METHODS: In this institutional review board–approved prospective study, a woman with triple-negative breast cancer (age, 49 years) underwent (13)C MRI after injection of hyperpolarized [1–carbon 13 {(13)C}]-pyruvate and DCE MRI at 3 T at baseline and after one cycle of neoadjuvant therapy. The (13)C-labeled lactate-to-pyruvate ratio derived from hyperpolarized (13)C MRI and the pharmacokinetic parameters transfer constant (K(trans)) and washout parameter (k(ep)) derived from DCE MRI were compared before and after treatment. RESULTS: Exchange of the (13)C label between injected hyperpolarized [1-(13)C]-pyruvate and the endogenous lactate pool was observed, catalyzed by the enzyme lactate dehydrogenase. After one cycle of neoadjuvant chemotherapy, a 34% reduction in the (13)C-labeled lactate-to-pyruvate ratio resulted in correct identification of the patient as a responder to therapy, which was subsequently confirmed via a complete pathologic response. However, DCE MRI showed an increase in mean K(trans) (132%) and mean k(ep) (31%), which could be incorrectly interpreted as a poor response to treatment. CONCLUSION: Hyperpolarized (13)C MRI enabled successful identification of breast cancer response after one cycle of neoadjuvant chemotherapy and may improve response prediction when used in conjunction with multiparametric proton MRI. Keywords: Breast, MR-Spectroscopy, Molecular Imaging-Cancer, Molecular Imaging-Clinical Translation, Neoplasms-Primary, Oncology, Tumor Response Published under a CC BY 4.0 license.
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spelling pubmed-73981162020-08-14 Hyperpolarized (13)C MRI of Tumor Metabolism Demonstrates Early Metabolic Response to Neoadjuvant Chemotherapy in Breast Cancer Woitek, Ramona McLean, Mary A. Gill, Andrew B. Grist, James T. Provenzano, Elena Patterson, Andrew J. Ursprung, Stephan Torheim, Turid Zaccagna, Fulvio Locke, Matthew Laurent, Marie-Christine Hilborne, Sarah Frary, Amy Beer, Lucian Rundo, Leonardo Patterson, Ilse Slough, Rhys Kane, Justine Biggs, Heather Harrison, Emma Lanz, Titus Basu, Bristi Baird, Richard Sala, Evis Graves, Martin J. Gilbert, Fiona J. Abraham, Jean E. Caldas, Carlos Brindle, Kevin M. Gallagher, Ferdia A. Radiol Imaging Cancer Technical Development PURPOSE: To compare hyperpolarized carbon 13 ((13)C) MRI with dynamic contrast material–enhanced (DCE) MRI in the detection of early treatment response in breast cancer. MATERIALS AND METHODS: In this institutional review board–approved prospective study, a woman with triple-negative breast cancer (age, 49 years) underwent (13)C MRI after injection of hyperpolarized [1–carbon 13 {(13)C}]-pyruvate and DCE MRI at 3 T at baseline and after one cycle of neoadjuvant therapy. The (13)C-labeled lactate-to-pyruvate ratio derived from hyperpolarized (13)C MRI and the pharmacokinetic parameters transfer constant (K(trans)) and washout parameter (k(ep)) derived from DCE MRI were compared before and after treatment. RESULTS: Exchange of the (13)C label between injected hyperpolarized [1-(13)C]-pyruvate and the endogenous lactate pool was observed, catalyzed by the enzyme lactate dehydrogenase. After one cycle of neoadjuvant chemotherapy, a 34% reduction in the (13)C-labeled lactate-to-pyruvate ratio resulted in correct identification of the patient as a responder to therapy, which was subsequently confirmed via a complete pathologic response. However, DCE MRI showed an increase in mean K(trans) (132%) and mean k(ep) (31%), which could be incorrectly interpreted as a poor response to treatment. CONCLUSION: Hyperpolarized (13)C MRI enabled successful identification of breast cancer response after one cycle of neoadjuvant chemotherapy and may improve response prediction when used in conjunction with multiparametric proton MRI. Keywords: Breast, MR-Spectroscopy, Molecular Imaging-Cancer, Molecular Imaging-Clinical Translation, Neoplasms-Primary, Oncology, Tumor Response Published under a CC BY 4.0 license. Radiological Society of North America 2020-07-31 /pmc/articles/PMC7398116/ /pubmed/32803167 http://dx.doi.org/10.1148/rycan.2020200017 Text en 2020 by the Radiological Society of North America, Inc. http://creativecommons.org/licenses/by/4.0/ Published under a (http://creativecommons.org/licenses/by/4.0/) CC BY 4.0 license.
spellingShingle Technical Development
Woitek, Ramona
McLean, Mary A.
Gill, Andrew B.
Grist, James T.
Provenzano, Elena
Patterson, Andrew J.
Ursprung, Stephan
Torheim, Turid
Zaccagna, Fulvio
Locke, Matthew
Laurent, Marie-Christine
Hilborne, Sarah
Frary, Amy
Beer, Lucian
Rundo, Leonardo
Patterson, Ilse
Slough, Rhys
Kane, Justine
Biggs, Heather
Harrison, Emma
Lanz, Titus
Basu, Bristi
Baird, Richard
Sala, Evis
Graves, Martin J.
Gilbert, Fiona J.
Abraham, Jean E.
Caldas, Carlos
Brindle, Kevin M.
Gallagher, Ferdia A.
Hyperpolarized (13)C MRI of Tumor Metabolism Demonstrates Early Metabolic Response to Neoadjuvant Chemotherapy in Breast Cancer
title Hyperpolarized (13)C MRI of Tumor Metabolism Demonstrates Early Metabolic Response to Neoadjuvant Chemotherapy in Breast Cancer
title_full Hyperpolarized (13)C MRI of Tumor Metabolism Demonstrates Early Metabolic Response to Neoadjuvant Chemotherapy in Breast Cancer
title_fullStr Hyperpolarized (13)C MRI of Tumor Metabolism Demonstrates Early Metabolic Response to Neoadjuvant Chemotherapy in Breast Cancer
title_full_unstemmed Hyperpolarized (13)C MRI of Tumor Metabolism Demonstrates Early Metabolic Response to Neoadjuvant Chemotherapy in Breast Cancer
title_short Hyperpolarized (13)C MRI of Tumor Metabolism Demonstrates Early Metabolic Response to Neoadjuvant Chemotherapy in Breast Cancer
title_sort hyperpolarized (13)c mri of tumor metabolism demonstrates early metabolic response to neoadjuvant chemotherapy in breast cancer
topic Technical Development
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7398116/
https://www.ncbi.nlm.nih.gov/pubmed/32803167
http://dx.doi.org/10.1148/rycan.2020200017
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