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Multiparametric MRI Analysis for the Identification of High Intensity Focused Ultrasound-Treated Tumor Tissue

PURPOSE: In this study endogenous magnetic resonance imaging (MRI) biomarkers for accurate segmentation of High Intensity Focused Ultrasound (HIFU)-treated tumor tissue and residual or recurring non-treated tumor tissue were identified. METHODS: Multiparametric MRI, consisting of quantitative T(1),...

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Detalles Bibliográficos
Autores principales: Hectors, Stefanie J. C. G., Jacobs, Igor, Strijkers, Gustav J., Nicolay, Klaas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057317/
https://www.ncbi.nlm.nih.gov/pubmed/24927280
http://dx.doi.org/10.1371/journal.pone.0099936
Descripción
Sumario:PURPOSE: In this study endogenous magnetic resonance imaging (MRI) biomarkers for accurate segmentation of High Intensity Focused Ultrasound (HIFU)-treated tumor tissue and residual or recurring non-treated tumor tissue were identified. METHODS: Multiparametric MRI, consisting of quantitative T(1), T(2), Apparent Diffusion Coefficient (ADC) and Magnetization Transfer Ratio (MTR) mapping, was performed in tumor-bearing mice before (n = 14), 1 h after (n = 14) and 72 h (n = 7) after HIFU treatment. A non-treated control group was included (n = 7). Cluster analysis using the Iterative Self Organizing Data Analysis (ISODATA) technique was performed on subsets of MRI parameters (feature vectors). The clusters resulting from the ISODATA segmentation were divided into a viable and non-viable class based on the fraction of pixels assigned to the clusters at the different experimental time points. ISODATA-derived non-viable tumor fractions were quantitatively compared to histology-derived non-viable tumor volume fractions. RESULTS: The highest agreement between the ISODATA-derived and histology-derived non-viable tumor fractions was observed for feature vector {T(1), T(2), ADC}. R(1) (1/T(1)), R(2) (1/T(2)), ADC and MTR each were significantly increased in the ISODATA-defined non-viable tumor tissue at 1 h after HIFU treatment compared to viable, non-treated tumor tissue. R(1), ADC and MTR were also significantly increased at 72 h after HIFU. CONCLUSIONS: This study demonstrates that non-viable, HIFU-treated tumor tissue can be distinguished from viable, non-treated tumor tissue using multiparametric MRI analysis. Clinical application of the presented methodology may allow for automated, accurate and objective evaluation of HIFU treatment.