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Dynamic contrast‐enhanced MRI perfusion for differentiating between melanoma and lung cancer brain metastases

Brain metastases originating from different primary sites overlap in appearance and are difficult to differentiate with conventional MRI. Dynamic contrast‐enhanced (DCE)‐MRI can assess tumor microvasculature and has demonstrated utility in characterizing primary brain tumors. Our aim was to evaluate...

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Autores principales: Hatzoglou, Vaios, Tisnado, Jamie, Mehta, Alpesh, Peck, Kyung K., Daras, Mariza, Omuro, Antonio M., Beal, Kathryn, Holodny, Andrei I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5387174/
https://www.ncbi.nlm.nih.gov/pubmed/28303695
http://dx.doi.org/10.1002/cam4.1046
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author Hatzoglou, Vaios
Tisnado, Jamie
Mehta, Alpesh
Peck, Kyung K.
Daras, Mariza
Omuro, Antonio M.
Beal, Kathryn
Holodny, Andrei I.
author_facet Hatzoglou, Vaios
Tisnado, Jamie
Mehta, Alpesh
Peck, Kyung K.
Daras, Mariza
Omuro, Antonio M.
Beal, Kathryn
Holodny, Andrei I.
author_sort Hatzoglou, Vaios
collection PubMed
description Brain metastases originating from different primary sites overlap in appearance and are difficult to differentiate with conventional MRI. Dynamic contrast‐enhanced (DCE)‐MRI can assess tumor microvasculature and has demonstrated utility in characterizing primary brain tumors. Our aim was to evaluate the performance of plasma volume (Vp) and volume transfer coefficient (K (trans)) derived from DCE‐MRI in distinguishing between melanoma and nonsmall cell lung cancer (NSCLC) brain metastases. Forty‐seven NSCLC and 23 melanoma brain metastases were retrospectively assessed with DCE‐MRI. Regions of interest were manually drawn around the metastases to calculate Vp(mean) and [Formula: see text]. The Mann–Whitney U test and receiver operating characteristic analysis (ROC) were performed to compare perfusion parameters between the two groups. The Vp(mean) of melanoma brain metastases (4.35, standard deviation [SD] = 1.31) was significantly higher (P = 0.03) than Vp(mean) of NSCLC brain metastases (2.27, SD = 0.96). The [Formula: see text] values were higher in melanoma brain metastases, but the difference between the two groups was not significant (P = 0.12). Based on ROC analysis, a cut‐off value of 3.02 for Vp(mean) (area under curve = 0.659 with SD = 0.074) distinguished between melanoma brain metastases and NSCLC brain metastases (P < 0.01) with 72% specificity. Our data show the DCE‐MRI parameter Vp(mean) can differentiate between melanoma and NSCLC brain metastases. The ability to noninvasively predict tumor histology of brain metastases in patients with multiple malignancies can have important clinical implications.
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spelling pubmed-53871742017-04-14 Dynamic contrast‐enhanced MRI perfusion for differentiating between melanoma and lung cancer brain metastases Hatzoglou, Vaios Tisnado, Jamie Mehta, Alpesh Peck, Kyung K. Daras, Mariza Omuro, Antonio M. Beal, Kathryn Holodny, Andrei I. Cancer Med Clinical Cancer Research Brain metastases originating from different primary sites overlap in appearance and are difficult to differentiate with conventional MRI. Dynamic contrast‐enhanced (DCE)‐MRI can assess tumor microvasculature and has demonstrated utility in characterizing primary brain tumors. Our aim was to evaluate the performance of plasma volume (Vp) and volume transfer coefficient (K (trans)) derived from DCE‐MRI in distinguishing between melanoma and nonsmall cell lung cancer (NSCLC) brain metastases. Forty‐seven NSCLC and 23 melanoma brain metastases were retrospectively assessed with DCE‐MRI. Regions of interest were manually drawn around the metastases to calculate Vp(mean) and [Formula: see text]. The Mann–Whitney U test and receiver operating characteristic analysis (ROC) were performed to compare perfusion parameters between the two groups. The Vp(mean) of melanoma brain metastases (4.35, standard deviation [SD] = 1.31) was significantly higher (P = 0.03) than Vp(mean) of NSCLC brain metastases (2.27, SD = 0.96). The [Formula: see text] values were higher in melanoma brain metastases, but the difference between the two groups was not significant (P = 0.12). Based on ROC analysis, a cut‐off value of 3.02 for Vp(mean) (area under curve = 0.659 with SD = 0.074) distinguished between melanoma brain metastases and NSCLC brain metastases (P < 0.01) with 72% specificity. Our data show the DCE‐MRI parameter Vp(mean) can differentiate between melanoma and NSCLC brain metastases. The ability to noninvasively predict tumor histology of brain metastases in patients with multiple malignancies can have important clinical implications. John Wiley and Sons Inc. 2017-03-17 /pmc/articles/PMC5387174/ /pubmed/28303695 http://dx.doi.org/10.1002/cam4.1046 Text en © 2017 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (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 Clinical Cancer Research
Hatzoglou, Vaios
Tisnado, Jamie
Mehta, Alpesh
Peck, Kyung K.
Daras, Mariza
Omuro, Antonio M.
Beal, Kathryn
Holodny, Andrei I.
Dynamic contrast‐enhanced MRI perfusion for differentiating between melanoma and lung cancer brain metastases
title Dynamic contrast‐enhanced MRI perfusion for differentiating between melanoma and lung cancer brain metastases
title_full Dynamic contrast‐enhanced MRI perfusion for differentiating between melanoma and lung cancer brain metastases
title_fullStr Dynamic contrast‐enhanced MRI perfusion for differentiating between melanoma and lung cancer brain metastases
title_full_unstemmed Dynamic contrast‐enhanced MRI perfusion for differentiating between melanoma and lung cancer brain metastases
title_short Dynamic contrast‐enhanced MRI perfusion for differentiating between melanoma and lung cancer brain metastases
title_sort dynamic contrast‐enhanced mri perfusion for differentiating between melanoma and lung cancer brain metastases
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5387174/
https://www.ncbi.nlm.nih.gov/pubmed/28303695
http://dx.doi.org/10.1002/cam4.1046
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