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A multitransmit external body array combined with a (1)H and (31)P endorectal coil to enable a multiparametric and multimetabolic MRI examination of the prostate at 7T

PURPOSE: In vivo (1)H and (31)P magnetic resonance spectroscopic imaging (MRSI) provide complementary information on the biology of prostate cancer. In this work we demonstrate the feasibility of performing multiparametric imaging (mpMRI) and (1)H and (31)P spectroscopic imaging of the prostate usin...

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Autores principales: Philips, Bart W. J., van Uden, Mark J., Rietsch, Stefan H. G., Orzada, Stephan, Scheenen, Tom W. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6852321/
https://www.ncbi.nlm.nih.gov/pubmed/31274201
http://dx.doi.org/10.1002/mp.13696
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author Philips, Bart W. J.
van Uden, Mark J.
Rietsch, Stefan H. G.
Orzada, Stephan
Scheenen, Tom W. J.
author_facet Philips, Bart W. J.
van Uden, Mark J.
Rietsch, Stefan H. G.
Orzada, Stephan
Scheenen, Tom W. J.
author_sort Philips, Bart W. J.
collection PubMed
description PURPOSE: In vivo (1)H and (31)P magnetic resonance spectroscopic imaging (MRSI) provide complementary information on the biology of prostate cancer. In this work we demonstrate the feasibility of performing multiparametric imaging (mpMRI) and (1)H and (31)P spectroscopic imaging of the prostate using a (31)P and (1)H endorectal radiofrequency coil (ERC) in combination with a multitransmit body array at 7 Tesla (T). METHODS: An ERC with a (31)P transceiver loop coil and (1)H receive (Rx) asymmetric microstrip ((31)P/(1)H ERC) was designed, constructed and tested in combination with an external 8‐channel (1)H transceiver body array coil (8CH). Electromagnetic field simulations and measurements and in vivo temperature measurements of the ERC were performed for safety validation. In addition, the signal‐to‐noise (SNR) benefit of the (1)H microstrip with respect to the 8CH was evaluated. Finally, the feasibility of the setup was tested in one volunteer and three patients with prostate cancer by performing T(2)‐weighted and diffusion‐weighted imaging in combination with (1)H and (31)P spectroscopic imaging. RESULTS: Electromagnetic field simulations of the (31)P loop coil showed no differences in the E‐ and B‐fields of the (31)P/(1)H ERC compared with a previously safety validated ERC without (1)H microstrip. The hotspot of the specific absorption rate (SAR) at the feed point of the (31)P/(1)H ERC loop coil was 9.42 W/kg when transmitting on (31)P at 1 W. Additional in vivo measurements showed a maximum temperature increase at the SAR hotspot of 0.7°C over 6 min on (31)P at 1.9 W transmit (Tx) power, indicating safe maximum power levels. When transmitting with the external (1)H body array at 40W for 2:30 min, the temperature increase around the ERC was < 0.3°C. Up to 3.5 cm into the prostate the (1)H microstrip of the ERC provided higher SNR than the 8CH. The total coil combination allowed acquisition of an mpMRI protocol and the assessment of (31)P and (1)H metabolites of the prostate in all test subjects. CONCLUSION: We developed a setup with a (31)P transceiver and (1)H Rx endorectal coil in combination with an 8‐channel transceiver external body array coil and demonstrated its safety and feasibility for obtaining multiparametric imaging and (1)H and (31)P MRSI at 7T in patients with prostate cancer within one MR examination.
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spelling pubmed-68523212019-11-22 A multitransmit external body array combined with a (1)H and (31)P endorectal coil to enable a multiparametric and multimetabolic MRI examination of the prostate at 7T Philips, Bart W. J. van Uden, Mark J. Rietsch, Stefan H. G. Orzada, Stephan Scheenen, Tom W. J. Med Phys DIAGNOSTIC IMAGING (IONIZING AND NON‐IONIZING) PURPOSE: In vivo (1)H and (31)P magnetic resonance spectroscopic imaging (MRSI) provide complementary information on the biology of prostate cancer. In this work we demonstrate the feasibility of performing multiparametric imaging (mpMRI) and (1)H and (31)P spectroscopic imaging of the prostate using a (31)P and (1)H endorectal radiofrequency coil (ERC) in combination with a multitransmit body array at 7 Tesla (T). METHODS: An ERC with a (31)P transceiver loop coil and (1)H receive (Rx) asymmetric microstrip ((31)P/(1)H ERC) was designed, constructed and tested in combination with an external 8‐channel (1)H transceiver body array coil (8CH). Electromagnetic field simulations and measurements and in vivo temperature measurements of the ERC were performed for safety validation. In addition, the signal‐to‐noise (SNR) benefit of the (1)H microstrip with respect to the 8CH was evaluated. Finally, the feasibility of the setup was tested in one volunteer and three patients with prostate cancer by performing T(2)‐weighted and diffusion‐weighted imaging in combination with (1)H and (31)P spectroscopic imaging. RESULTS: Electromagnetic field simulations of the (31)P loop coil showed no differences in the E‐ and B‐fields of the (31)P/(1)H ERC compared with a previously safety validated ERC without (1)H microstrip. The hotspot of the specific absorption rate (SAR) at the feed point of the (31)P/(1)H ERC loop coil was 9.42 W/kg when transmitting on (31)P at 1 W. Additional in vivo measurements showed a maximum temperature increase at the SAR hotspot of 0.7°C over 6 min on (31)P at 1.9 W transmit (Tx) power, indicating safe maximum power levels. When transmitting with the external (1)H body array at 40W for 2:30 min, the temperature increase around the ERC was < 0.3°C. Up to 3.5 cm into the prostate the (1)H microstrip of the ERC provided higher SNR than the 8CH. The total coil combination allowed acquisition of an mpMRI protocol and the assessment of (31)P and (1)H metabolites of the prostate in all test subjects. CONCLUSION: We developed a setup with a (31)P transceiver and (1)H Rx endorectal coil in combination with an 8‐channel transceiver external body array coil and demonstrated its safety and feasibility for obtaining multiparametric imaging and (1)H and (31)P MRSI at 7T in patients with prostate cancer within one MR examination. John Wiley and Sons Inc. 2019-08-01 2019-09 /pmc/articles/PMC6852321/ /pubmed/31274201 http://dx.doi.org/10.1002/mp.13696 Text en © 2019 The Authors. Medical Physics published by Wiley Periodicals, Inc. on behalf of American Association of Physicists in Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle DIAGNOSTIC IMAGING (IONIZING AND NON‐IONIZING)
Philips, Bart W. J.
van Uden, Mark J.
Rietsch, Stefan H. G.
Orzada, Stephan
Scheenen, Tom W. J.
A multitransmit external body array combined with a (1)H and (31)P endorectal coil to enable a multiparametric and multimetabolic MRI examination of the prostate at 7T
title A multitransmit external body array combined with a (1)H and (31)P endorectal coil to enable a multiparametric and multimetabolic MRI examination of the prostate at 7T
title_full A multitransmit external body array combined with a (1)H and (31)P endorectal coil to enable a multiparametric and multimetabolic MRI examination of the prostate at 7T
title_fullStr A multitransmit external body array combined with a (1)H and (31)P endorectal coil to enable a multiparametric and multimetabolic MRI examination of the prostate at 7T
title_full_unstemmed A multitransmit external body array combined with a (1)H and (31)P endorectal coil to enable a multiparametric and multimetabolic MRI examination of the prostate at 7T
title_short A multitransmit external body array combined with a (1)H and (31)P endorectal coil to enable a multiparametric and multimetabolic MRI examination of the prostate at 7T
title_sort multitransmit external body array combined with a (1)h and (31)p endorectal coil to enable a multiparametric and multimetabolic mri examination of the prostate at 7t
topic DIAGNOSTIC IMAGING (IONIZING AND NON‐IONIZING)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6852321/
https://www.ncbi.nlm.nih.gov/pubmed/31274201
http://dx.doi.org/10.1002/mp.13696
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