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Hyperpolarized 13C MRI: Path to Clinical Translation in Oncology

Publikation: Bidrag til tidsskriftReviewForskningpeer review

Harvard

Kurhanewicz, J, Vigneron, DB, Ardenkjaer-Larsen, JH, Bankson, JA, Brindle, K, Cunningham, CH, Gallagher, FA, Keshari, KR, Kjaer, A, Laustsen, C, Mankoff, DA, Merritt, ME, Nelson, SJ, Pauly, JM, Lee, P, Ronen, S, Tyler, DJ, Rajan, SS, Spielman, DM, Wald, L, Zhang, X, Malloy, CR & Rizi, R 2019, 'Hyperpolarized 13C MRI: Path to Clinical Translation in Oncology' Neoplasia (New York, N.Y.), bind 21, nr. 1, s. 1-16. https://doi.org/10.1016/j.neo.2018.09.006

APA

Kurhanewicz, J., Vigneron, D. B., Ardenkjaer-Larsen, J. H., Bankson, J. A., Brindle, K., Cunningham, C. H., ... Rizi, R. (2019). Hyperpolarized 13C MRI: Path to Clinical Translation in Oncology. Neoplasia (New York, N.Y.), 21(1), 1-16. https://doi.org/10.1016/j.neo.2018.09.006

CBE

Kurhanewicz J, Vigneron DB, Ardenkjaer-Larsen JH, Bankson JA, Brindle K, Cunningham CH, Gallagher FA, Keshari KR, Kjaer A, Laustsen C, Mankoff DA, Merritt ME, Nelson SJ, Pauly JM, Lee P, Ronen S, Tyler DJ, Rajan SS, Spielman DM, Wald L, Zhang X, Malloy CR, Rizi R. 2019. Hyperpolarized 13C MRI: Path to Clinical Translation in Oncology. Neoplasia (New York, N.Y.). 21(1):1-16. https://doi.org/10.1016/j.neo.2018.09.006

MLA

Vancouver

Kurhanewicz J, Vigneron DB, Ardenkjaer-Larsen JH, Bankson JA, Brindle K, Cunningham CH o.a. Hyperpolarized 13C MRI: Path to Clinical Translation in Oncology. Neoplasia (New York, N.Y.). 2019 jan;21(1):1-16. https://doi.org/10.1016/j.neo.2018.09.006

Author

Kurhanewicz, John ; Vigneron, Daniel B ; Ardenkjaer-Larsen, Jan Henrik ; Bankson, James A ; Brindle, Kevin ; Cunningham, Charles H ; Gallagher, Ferdia A ; Keshari, Kayvan R ; Kjaer, Andreas ; Laustsen, Christoffer ; Mankoff, David A ; Merritt, Matthew E ; Nelson, Sarah J ; Pauly, John M ; Lee, Philips ; Ronen, Sabrina ; Tyler, Damian J ; Rajan, Sunder S ; Spielman, Daniel M ; Wald, Lawrence ; Zhang, Xiaoliang ; Malloy, Craig R ; Rizi, Rahim. / Hyperpolarized 13C MRI : Path to Clinical Translation in Oncology. I: Neoplasia (New York, N.Y.). 2019 ; Bind 21, Nr. 1. s. 1-16.

Bibtex

@article{bb1885a57eaa4d4ba220bdf4c2f571af,
title = "Hyperpolarized 13C MRI: Path to Clinical Translation in Oncology",
abstract = "This white paper discusses prospects for advancing hyperpolarization technology to better understand cancer metabolism, identify current obstacles to HP (hyperpolarized) 13C magnetic resonance imaging's (MRI's) widespread clinical use, and provide recommendations for overcoming them. Since the publication of the first NIH white paper on hyperpolarized 13C MRI in 2011, preclinical studies involving [1-13C]pyruvate as well a number of other 13C labeled metabolic substrates have demonstrated this technology's capacity to provide unique metabolic information. A dose-ranging study of HP [1-13C]pyruvate in patients with prostate cancer established safety and feasibility of this technique. Additional studies are ongoing in prostate, brain, breast, liver, cervical, and ovarian cancer. Technology for generating and delivering hyperpolarized agents has evolved, and new MR data acquisition sequences and improved MRI hardware have been developed. It will be important to continue investigation and development of existing and new probes in animal models. Improved polarization technology, efficient radiofrequency coils, and reliable pulse sequences are all important objectives to enable exploration of the technology in healthy control subjects and patient populations. It will be critical to determine how HP 13C MRI might fill existing needs in current clinical research and practice, and complement existing metabolic imaging modalities. Financial sponsorship and integration of academia, industry, and government efforts will be important factors in translating the technology for clinical research in oncology. This white paper is intended to provide recommendations with this goal in mind.",
keywords = "Animals, Carbon Isotopes, Disease Models, Animal, Humans, Magnetic Resonance Imaging/methods, Neoplasms/diagnosis, Reproducibility of Results, Translational Medical Research",
author = "John Kurhanewicz and Vigneron, {Daniel B} and Ardenkjaer-Larsen, {Jan Henrik} and Bankson, {James A} and Kevin Brindle and Cunningham, {Charles H} and Gallagher, {Ferdia A} and Keshari, {Kayvan R} and Andreas Kjaer and Christoffer Laustsen and Mankoff, {David A} and Merritt, {Matthew E} and Nelson, {Sarah J} and Pauly, {John M} and Philips Lee and Sabrina Ronen and Tyler, {Damian J} and Rajan, {Sunder S} and Spielman, {Daniel M} and Lawrence Wald and Xiaoliang Zhang and Malloy, {Craig R} and Rahim Rizi",
note = "Copyright {\circledC} 2018 The Authors. Published by Elsevier Inc. All rights reserved.",
year = "2019",
month = "1",
doi = "10.1016/j.neo.2018.09.006",
language = "English",
volume = "21",
pages = "1--16",
journal = "Neoplasia",
issn = "1522-8002",
publisher = "Neoplasia Press",
number = "1",

}

RIS

TY - JOUR

T1 - Hyperpolarized 13C MRI

T2 - Path to Clinical Translation in Oncology

AU - Kurhanewicz, John

AU - Vigneron, Daniel B

AU - Ardenkjaer-Larsen, Jan Henrik

AU - Bankson, James A

AU - Brindle, Kevin

AU - Cunningham, Charles H

AU - Gallagher, Ferdia A

AU - Keshari, Kayvan R

AU - Kjaer, Andreas

AU - Laustsen, Christoffer

AU - Mankoff, David A

AU - Merritt, Matthew E

AU - Nelson, Sarah J

AU - Pauly, John M

AU - Lee, Philips

AU - Ronen, Sabrina

AU - Tyler, Damian J

AU - Rajan, Sunder S

AU - Spielman, Daniel M

AU - Wald, Lawrence

AU - Zhang, Xiaoliang

AU - Malloy, Craig R

AU - Rizi, Rahim

N1 - Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved.

PY - 2019/1

Y1 - 2019/1

N2 - This white paper discusses prospects for advancing hyperpolarization technology to better understand cancer metabolism, identify current obstacles to HP (hyperpolarized) 13C magnetic resonance imaging's (MRI's) widespread clinical use, and provide recommendations for overcoming them. Since the publication of the first NIH white paper on hyperpolarized 13C MRI in 2011, preclinical studies involving [1-13C]pyruvate as well a number of other 13C labeled metabolic substrates have demonstrated this technology's capacity to provide unique metabolic information. A dose-ranging study of HP [1-13C]pyruvate in patients with prostate cancer established safety and feasibility of this technique. Additional studies are ongoing in prostate, brain, breast, liver, cervical, and ovarian cancer. Technology for generating and delivering hyperpolarized agents has evolved, and new MR data acquisition sequences and improved MRI hardware have been developed. It will be important to continue investigation and development of existing and new probes in animal models. Improved polarization technology, efficient radiofrequency coils, and reliable pulse sequences are all important objectives to enable exploration of the technology in healthy control subjects and patient populations. It will be critical to determine how HP 13C MRI might fill existing needs in current clinical research and practice, and complement existing metabolic imaging modalities. Financial sponsorship and integration of academia, industry, and government efforts will be important factors in translating the technology for clinical research in oncology. This white paper is intended to provide recommendations with this goal in mind.

AB - This white paper discusses prospects for advancing hyperpolarization technology to better understand cancer metabolism, identify current obstacles to HP (hyperpolarized) 13C magnetic resonance imaging's (MRI's) widespread clinical use, and provide recommendations for overcoming them. Since the publication of the first NIH white paper on hyperpolarized 13C MRI in 2011, preclinical studies involving [1-13C]pyruvate as well a number of other 13C labeled metabolic substrates have demonstrated this technology's capacity to provide unique metabolic information. A dose-ranging study of HP [1-13C]pyruvate in patients with prostate cancer established safety and feasibility of this technique. Additional studies are ongoing in prostate, brain, breast, liver, cervical, and ovarian cancer. Technology for generating and delivering hyperpolarized agents has evolved, and new MR data acquisition sequences and improved MRI hardware have been developed. It will be important to continue investigation and development of existing and new probes in animal models. Improved polarization technology, efficient radiofrequency coils, and reliable pulse sequences are all important objectives to enable exploration of the technology in healthy control subjects and patient populations. It will be critical to determine how HP 13C MRI might fill existing needs in current clinical research and practice, and complement existing metabolic imaging modalities. Financial sponsorship and integration of academia, industry, and government efforts will be important factors in translating the technology for clinical research in oncology. This white paper is intended to provide recommendations with this goal in mind.

KW - Animals

KW - Carbon Isotopes

KW - Disease Models, Animal

KW - Humans

KW - Magnetic Resonance Imaging/methods

KW - Neoplasms/diagnosis

KW - Reproducibility of Results

KW - Translational Medical Research

UR - http://www.scopus.com/inward/record.url?scp=85056925374&partnerID=8YFLogxK

U2 - 10.1016/j.neo.2018.09.006

DO - 10.1016/j.neo.2018.09.006

M3 - Review

VL - 21

SP - 1

EP - 16

JO - Neoplasia

JF - Neoplasia

SN - 1522-8002

IS - 1

ER -

ID: 56695101