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Diffusion weighted MRI as an early predictor of tumor response to hypofractionated stereotactic boost for prostate cancer

We evaluated the feasibility of using the kinetic of diffusion-weighted MRI (DWI) and the normalized apparent coefficient diffusion (ADC) map value as an early biomarker in patients treated by external beam radiotherapy (EBRT). Twelve patients were included within the frame of a multicenter phase II...

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Autores principales: Pasquier, David, Hadj Henni, Abderraouf, Escande, Alexandre, Tresch, Emmanuelle, Reynaert, Nick, Colot, Olivier, Lartigau, Eric, Betrouni, Nacim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6039515/
https://www.ncbi.nlm.nih.gov/pubmed/29991748
http://dx.doi.org/10.1038/s41598-018-28817-9
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author Pasquier, David
Hadj Henni, Abderraouf
Escande, Alexandre
Tresch, Emmanuelle
Reynaert, Nick
Colot, Olivier
Lartigau, Eric
Betrouni, Nacim
author_facet Pasquier, David
Hadj Henni, Abderraouf
Escande, Alexandre
Tresch, Emmanuelle
Reynaert, Nick
Colot, Olivier
Lartigau, Eric
Betrouni, Nacim
author_sort Pasquier, David
collection PubMed
description We evaluated the feasibility of using the kinetic of diffusion-weighted MRI (DWI) and the normalized apparent coefficient diffusion (ADC) map value as an early biomarker in patients treated by external beam radiotherapy (EBRT). Twelve patients were included within the frame of a multicenter phase II trial and treated for intermediate risk prostate cancer (PCa). Multiparametric MRI was performed before treatment (M0) and every 6 months until M24. Association between nADC and PSA or PSA kinetic was evaluated using the test of nullity of the Spearman correlation coefficient. The median rates of PSA at the time of diagnosis, two years and four years after EBRT were 9.29 ng/ml (range from 5.26 to 17.67), 0.68 ng/ml (0.07–2.7), 0.47 ng/ml (0.09–1.39), respectively. Median nADC increased from 1.14 × 10(−3) mm(2)/s to 1.59 × 10(−3) mm(2)/s between M0 and M24. Only one patient presented a decrease of nADC (1.35 × 10(−3) mm(2)/s and 1.11 × 10(−3) mm(2)/s at M0 and M12 respectively). The increase in nADC at M6 was correlated with PSA decrease at M18, M24 and M30 (p < 0.05). The increase in nADc at M12 was correlated with PSA decrease at M36 (p = 0.019). Early nADC variation were correlated with late PSA decrease for patients with PCa treated by EBRT.
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spelling pubmed-60395152018-07-12 Diffusion weighted MRI as an early predictor of tumor response to hypofractionated stereotactic boost for prostate cancer Pasquier, David Hadj Henni, Abderraouf Escande, Alexandre Tresch, Emmanuelle Reynaert, Nick Colot, Olivier Lartigau, Eric Betrouni, Nacim Sci Rep Article We evaluated the feasibility of using the kinetic of diffusion-weighted MRI (DWI) and the normalized apparent coefficient diffusion (ADC) map value as an early biomarker in patients treated by external beam radiotherapy (EBRT). Twelve patients were included within the frame of a multicenter phase II trial and treated for intermediate risk prostate cancer (PCa). Multiparametric MRI was performed before treatment (M0) and every 6 months until M24. Association between nADC and PSA or PSA kinetic was evaluated using the test of nullity of the Spearman correlation coefficient. The median rates of PSA at the time of diagnosis, two years and four years after EBRT were 9.29 ng/ml (range from 5.26 to 17.67), 0.68 ng/ml (0.07–2.7), 0.47 ng/ml (0.09–1.39), respectively. Median nADC increased from 1.14 × 10(−3) mm(2)/s to 1.59 × 10(−3) mm(2)/s between M0 and M24. Only one patient presented a decrease of nADC (1.35 × 10(−3) mm(2)/s and 1.11 × 10(−3) mm(2)/s at M0 and M12 respectively). The increase in nADC at M6 was correlated with PSA decrease at M18, M24 and M30 (p < 0.05). The increase in nADc at M12 was correlated with PSA decrease at M36 (p = 0.019). Early nADC variation were correlated with late PSA decrease for patients with PCa treated by EBRT. Nature Publishing Group UK 2018-07-10 /pmc/articles/PMC6039515/ /pubmed/29991748 http://dx.doi.org/10.1038/s41598-018-28817-9 Text en © The Author(s) 2018 Open Access 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 http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Pasquier, David
Hadj Henni, Abderraouf
Escande, Alexandre
Tresch, Emmanuelle
Reynaert, Nick
Colot, Olivier
Lartigau, Eric
Betrouni, Nacim
Diffusion weighted MRI as an early predictor of tumor response to hypofractionated stereotactic boost for prostate cancer
title Diffusion weighted MRI as an early predictor of tumor response to hypofractionated stereotactic boost for prostate cancer
title_full Diffusion weighted MRI as an early predictor of tumor response to hypofractionated stereotactic boost for prostate cancer
title_fullStr Diffusion weighted MRI as an early predictor of tumor response to hypofractionated stereotactic boost for prostate cancer
title_full_unstemmed Diffusion weighted MRI as an early predictor of tumor response to hypofractionated stereotactic boost for prostate cancer
title_short Diffusion weighted MRI as an early predictor of tumor response to hypofractionated stereotactic boost for prostate cancer
title_sort diffusion weighted mri as an early predictor of tumor response to hypofractionated stereotactic boost for prostate cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6039515/
https://www.ncbi.nlm.nih.gov/pubmed/29991748
http://dx.doi.org/10.1038/s41598-018-28817-9
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