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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 (...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Radiological Society of North America
2020
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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. |
format | Online Article Text |
id | pubmed-7398116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Radiological Society of North America |
record_format | MEDLINE/PubMed |
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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