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Monitoring temozolomide treatment of low-grade glioma with proton magnetic resonance spectroscopy

Assessment of low-grade glioma treatment response remains as much of a challenge as the treatment itself. Proton magnetic resonance spectroscopy ((1)H-MRS) and imaging were incorporated into a study of patients receiving temozolomide therapy for low-grade glioma in order to evaluate and monitor tumo...

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Autores principales: Murphy, P S, Viviers, L, Abson, C, Rowland, I J, Brada, M, Leach, M O, Dzik-Jurasz, A S K
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2410174/
https://www.ncbi.nlm.nih.gov/pubmed/14970853
http://dx.doi.org/10.1038/sj.bjc.6601593
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author Murphy, P S
Viviers, L
Abson, C
Rowland, I J
Brada, M
Leach, M O
Dzik-Jurasz, A S K
author_facet Murphy, P S
Viviers, L
Abson, C
Rowland, I J
Brada, M
Leach, M O
Dzik-Jurasz, A S K
author_sort Murphy, P S
collection PubMed
description Assessment of low-grade glioma treatment response remains as much of a challenge as the treatment itself. Proton magnetic resonance spectroscopy ((1)H-MRS) and imaging were incorporated into a study of patients receiving temozolomide therapy for low-grade glioma in order to evaluate and monitor tumour metabolite and volume changes during treatment. Patients (n=12) received oral temozolomide (200 mg m(−2) day(−1)) over 5 days on a 28-day cycle for 12 cycles. Response assessment included baseline and three-monthly magnetic resonance imaging studies (pretreatment, 3, 6, 9 and 12 months) assessing the tumour size. Short (TE (echo time)=20 ms) and long (TE=135 ms) echo time single voxel spectroscopy was performed in parallel to determine metabolite profiles. The mean tumour volume change at the end of treatment was −33% (s.d.=20). The dominant metabolite in long echo time spectra was choline. At 12 months, a significant reduction in the mean choline signal was observed compared with the pretreatment (P=0.035) and 3-month scan (P=0.021). The reduction in the tumour choline/water signal paralleled tumour volume change and may reflect the therapeutic effect of temozolomide.
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spelling pubmed-24101742009-09-10 Monitoring temozolomide treatment of low-grade glioma with proton magnetic resonance spectroscopy Murphy, P S Viviers, L Abson, C Rowland, I J Brada, M Leach, M O Dzik-Jurasz, A S K Br J Cancer Clinical Assessment of low-grade glioma treatment response remains as much of a challenge as the treatment itself. Proton magnetic resonance spectroscopy ((1)H-MRS) and imaging were incorporated into a study of patients receiving temozolomide therapy for low-grade glioma in order to evaluate and monitor tumour metabolite and volume changes during treatment. Patients (n=12) received oral temozolomide (200 mg m(−2) day(−1)) over 5 days on a 28-day cycle for 12 cycles. Response assessment included baseline and three-monthly magnetic resonance imaging studies (pretreatment, 3, 6, 9 and 12 months) assessing the tumour size. Short (TE (echo time)=20 ms) and long (TE=135 ms) echo time single voxel spectroscopy was performed in parallel to determine metabolite profiles. The mean tumour volume change at the end of treatment was −33% (s.d.=20). The dominant metabolite in long echo time spectra was choline. At 12 months, a significant reduction in the mean choline signal was observed compared with the pretreatment (P=0.035) and 3-month scan (P=0.021). The reduction in the tumour choline/water signal paralleled tumour volume change and may reflect the therapeutic effect of temozolomide. Nature Publishing Group 2004-02-23 2004-02-17 /pmc/articles/PMC2410174/ /pubmed/14970853 http://dx.doi.org/10.1038/sj.bjc.6601593 Text en Copyright © 2004 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Clinical
Murphy, P S
Viviers, L
Abson, C
Rowland, I J
Brada, M
Leach, M O
Dzik-Jurasz, A S K
Monitoring temozolomide treatment of low-grade glioma with proton magnetic resonance spectroscopy
title Monitoring temozolomide treatment of low-grade glioma with proton magnetic resonance spectroscopy
title_full Monitoring temozolomide treatment of low-grade glioma with proton magnetic resonance spectroscopy
title_fullStr Monitoring temozolomide treatment of low-grade glioma with proton magnetic resonance spectroscopy
title_full_unstemmed Monitoring temozolomide treatment of low-grade glioma with proton magnetic resonance spectroscopy
title_short Monitoring temozolomide treatment of low-grade glioma with proton magnetic resonance spectroscopy
title_sort monitoring temozolomide treatment of low-grade glioma with proton magnetic resonance spectroscopy
topic Clinical
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2410174/
https://www.ncbi.nlm.nih.gov/pubmed/14970853
http://dx.doi.org/10.1038/sj.bjc.6601593
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