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T(1ρ) for Radiotherapy Treatment Response Monitoring in Rectal Cancer Patients: A Pilot Study
Quantitative MRI has the potential to produce imaging biomarkers for the prediction of early response to radiotherapy treatment. In this pilot study, a potential imaging biomarker, the T(1ρ) relaxation time, is assessed for this purpose. A T(1ρ) sequence was implemented on a 1.5 T MR-linac system, a...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8999631/ https://www.ncbi.nlm.nih.gov/pubmed/35407606 http://dx.doi.org/10.3390/jcm11071998 |
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author | Kooreman, Ernst S. Tanaka, Max ter Beek, Leon C. Peters, Femke P. Marijnen, Corrie A. M. van der Heide, Uulke A. van Houdt, Petra J. |
author_facet | Kooreman, Ernst S. Tanaka, Max ter Beek, Leon C. Peters, Femke P. Marijnen, Corrie A. M. van der Heide, Uulke A. van Houdt, Petra J. |
author_sort | Kooreman, Ernst S. |
collection | PubMed |
description | Quantitative MRI has the potential to produce imaging biomarkers for the prediction of early response to radiotherapy treatment. In this pilot study, a potential imaging biomarker, the T(1ρ) relaxation time, is assessed for this purpose. A T(1ρ) sequence was implemented on a 1.5 T MR-linac system, a system that combines an MRI with a linear accelerator for radiation treatment. An agar phantom with concentrations of 1–4% w/w was constructed for technical validation of the sequence. Phantom images were assessed in terms of short-term repeatability and signal-to-noise ratio. Twelve rectal cancer patients, who were treated with 5 × 5 Gy, were imaged on each treatment fraction. Individual changes in the T(1ρ) values of the gross tumor volume (GTV) showed an increase for most patients, although a paired t-test comparing values in the GTV from the first to the last treatment fraction showed no statistically significant difference. The phantom measurements showed excellent short-term repeatability (0.5–1.5 ms), and phantom T(1ρ) values corresponded to the literature values. T(1ρ) imaging was implemented successfully on the MR-linac, with a repeatability comparable to diagnostic systems, although clinical benefit in terms of treatment response monitoring remains to be demonstrated. |
format | Online Article Text |
id | pubmed-8999631 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-89996312022-04-12 T(1ρ) for Radiotherapy Treatment Response Monitoring in Rectal Cancer Patients: A Pilot Study Kooreman, Ernst S. Tanaka, Max ter Beek, Leon C. Peters, Femke P. Marijnen, Corrie A. M. van der Heide, Uulke A. van Houdt, Petra J. J Clin Med Article Quantitative MRI has the potential to produce imaging biomarkers for the prediction of early response to radiotherapy treatment. In this pilot study, a potential imaging biomarker, the T(1ρ) relaxation time, is assessed for this purpose. A T(1ρ) sequence was implemented on a 1.5 T MR-linac system, a system that combines an MRI with a linear accelerator for radiation treatment. An agar phantom with concentrations of 1–4% w/w was constructed for technical validation of the sequence. Phantom images were assessed in terms of short-term repeatability and signal-to-noise ratio. Twelve rectal cancer patients, who were treated with 5 × 5 Gy, were imaged on each treatment fraction. Individual changes in the T(1ρ) values of the gross tumor volume (GTV) showed an increase for most patients, although a paired t-test comparing values in the GTV from the first to the last treatment fraction showed no statistically significant difference. The phantom measurements showed excellent short-term repeatability (0.5–1.5 ms), and phantom T(1ρ) values corresponded to the literature values. T(1ρ) imaging was implemented successfully on the MR-linac, with a repeatability comparable to diagnostic systems, although clinical benefit in terms of treatment response monitoring remains to be demonstrated. MDPI 2022-04-02 /pmc/articles/PMC8999631/ /pubmed/35407606 http://dx.doi.org/10.3390/jcm11071998 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kooreman, Ernst S. Tanaka, Max ter Beek, Leon C. Peters, Femke P. Marijnen, Corrie A. M. van der Heide, Uulke A. van Houdt, Petra J. T(1ρ) for Radiotherapy Treatment Response Monitoring in Rectal Cancer Patients: A Pilot Study |
title | T(1ρ) for Radiotherapy Treatment Response Monitoring in Rectal Cancer Patients: A Pilot Study |
title_full | T(1ρ) for Radiotherapy Treatment Response Monitoring in Rectal Cancer Patients: A Pilot Study |
title_fullStr | T(1ρ) for Radiotherapy Treatment Response Monitoring in Rectal Cancer Patients: A Pilot Study |
title_full_unstemmed | T(1ρ) for Radiotherapy Treatment Response Monitoring in Rectal Cancer Patients: A Pilot Study |
title_short | T(1ρ) for Radiotherapy Treatment Response Monitoring in Rectal Cancer Patients: A Pilot Study |
title_sort | t(1ρ) for radiotherapy treatment response monitoring in rectal cancer patients: a pilot study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8999631/ https://www.ncbi.nlm.nih.gov/pubmed/35407606 http://dx.doi.org/10.3390/jcm11071998 |
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