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Imaging and histopathologic correlates of plasma cell-free DNA concentration and circulating tumor DNA in adult patients with newly diagnosed glioblastoma

BACKGROUND: Plasma cell-free DNA (cfDNA) concentration is lower in glioblastoma (GBM) compared to other solid tumors, which can lead to low circulating tumor DNA (ctDNA) detection. In this study, we investigated the relationship between multimodality magnetic resonance imaging (MRI) and histopatholo...

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Autores principales: Nabavizadeh, Seyed Ali, Ware, Jeffrey B, Guiry, Samantha, Nasrallah, MacLean P, Mays, Jazmine J, Till, Jacob E, Hussain, Jasmin, Abdalla, Aseel, Yee, Stephanie S, Binder, Zev A, O’Rourke, Donald M, Brem, Steven, Desai, Arati S, Wolf, Ronald, Carpenter, Erica L, Bagley, Stephen J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7045782/
https://www.ncbi.nlm.nih.gov/pubmed/32140683
http://dx.doi.org/10.1093/noajnl/vdaa016
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author Nabavizadeh, Seyed Ali
Ware, Jeffrey B
Guiry, Samantha
Nasrallah, MacLean P
Mays, Jazmine J
Till, Jacob E
Hussain, Jasmin
Abdalla, Aseel
Yee, Stephanie S
Binder, Zev A
O’Rourke, Donald M
Brem, Steven
Desai, Arati S
Wolf, Ronald
Carpenter, Erica L
Bagley, Stephen J
author_facet Nabavizadeh, Seyed Ali
Ware, Jeffrey B
Guiry, Samantha
Nasrallah, MacLean P
Mays, Jazmine J
Till, Jacob E
Hussain, Jasmin
Abdalla, Aseel
Yee, Stephanie S
Binder, Zev A
O’Rourke, Donald M
Brem, Steven
Desai, Arati S
Wolf, Ronald
Carpenter, Erica L
Bagley, Stephen J
author_sort Nabavizadeh, Seyed Ali
collection PubMed
description BACKGROUND: Plasma cell-free DNA (cfDNA) concentration is lower in glioblastoma (GBM) compared to other solid tumors, which can lead to low circulating tumor DNA (ctDNA) detection. In this study, we investigated the relationship between multimodality magnetic resonance imaging (MRI) and histopathologic features with plasma cfDNA concentration and ctDNA detection in patients with treatment-naive GBM. METHODS: We analyzed plasma cfDNA concentration, MRI scans, and tumor histopathology from 42 adult patients with newly diagnosed GBM. Linear regression analysis was used to examine the relationship of plasma cfDNA concentration before surgery to imaging and histopathologic characteristics. In a subset of patients, imaging and histopathologic metrics were also compared between patients with and without a detected tumor somatic mutation. RESULTS: Tumor volume with elevated (>1.5 times contralateral white matter) rate transfer constant (K(ep), a surrogate of blood–brain barrier [BBB] permeability) was independently associated with plasma cfDNA concentration (P = .001). Histopathologic characteristics independently associated with plasma cfDNA concentration included CD68+ macrophage density (P = .01) and size of tumor vessels (P = .01). Patients with higher (grade ≥3) perivascular CD68+ macrophage density had lower volume transfer constant (K(trans), P = .01) compared to those with lower perivascular CD68+ macrophage density. Detection of at least 1 somatic mutation in plasma cfDNA was associated with significantly lower perivascular CD68+ macrophages (P = .01). CONCLUSIONS: Metrics of BBB disruption and quantity and distribution of tumor-associated macrophages are associated with plasma cfDNA concentration and ctDNA detection in GBM patients. These findings represent an important step in understanding the factors that determine plasma cfDNA concentration and ctDNA detection.
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spelling pubmed-70457822020-03-03 Imaging and histopathologic correlates of plasma cell-free DNA concentration and circulating tumor DNA in adult patients with newly diagnosed glioblastoma Nabavizadeh, Seyed Ali Ware, Jeffrey B Guiry, Samantha Nasrallah, MacLean P Mays, Jazmine J Till, Jacob E Hussain, Jasmin Abdalla, Aseel Yee, Stephanie S Binder, Zev A O’Rourke, Donald M Brem, Steven Desai, Arati S Wolf, Ronald Carpenter, Erica L Bagley, Stephen J Neurooncol Adv Clinical Investigations BACKGROUND: Plasma cell-free DNA (cfDNA) concentration is lower in glioblastoma (GBM) compared to other solid tumors, which can lead to low circulating tumor DNA (ctDNA) detection. In this study, we investigated the relationship between multimodality magnetic resonance imaging (MRI) and histopathologic features with plasma cfDNA concentration and ctDNA detection in patients with treatment-naive GBM. METHODS: We analyzed plasma cfDNA concentration, MRI scans, and tumor histopathology from 42 adult patients with newly diagnosed GBM. Linear regression analysis was used to examine the relationship of plasma cfDNA concentration before surgery to imaging and histopathologic characteristics. In a subset of patients, imaging and histopathologic metrics were also compared between patients with and without a detected tumor somatic mutation. RESULTS: Tumor volume with elevated (>1.5 times contralateral white matter) rate transfer constant (K(ep), a surrogate of blood–brain barrier [BBB] permeability) was independently associated with plasma cfDNA concentration (P = .001). Histopathologic characteristics independently associated with plasma cfDNA concentration included CD68+ macrophage density (P = .01) and size of tumor vessels (P = .01). Patients with higher (grade ≥3) perivascular CD68+ macrophage density had lower volume transfer constant (K(trans), P = .01) compared to those with lower perivascular CD68+ macrophage density. Detection of at least 1 somatic mutation in plasma cfDNA was associated with significantly lower perivascular CD68+ macrophages (P = .01). CONCLUSIONS: Metrics of BBB disruption and quantity and distribution of tumor-associated macrophages are associated with plasma cfDNA concentration and ctDNA detection in GBM patients. These findings represent an important step in understanding the factors that determine plasma cfDNA concentration and ctDNA detection. Oxford University Press 2020-02-27 /pmc/articles/PMC7045782/ /pubmed/32140683 http://dx.doi.org/10.1093/noajnl/vdaa016 Text en © The Author(s) 2020. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Investigations
Nabavizadeh, Seyed Ali
Ware, Jeffrey B
Guiry, Samantha
Nasrallah, MacLean P
Mays, Jazmine J
Till, Jacob E
Hussain, Jasmin
Abdalla, Aseel
Yee, Stephanie S
Binder, Zev A
O’Rourke, Donald M
Brem, Steven
Desai, Arati S
Wolf, Ronald
Carpenter, Erica L
Bagley, Stephen J
Imaging and histopathologic correlates of plasma cell-free DNA concentration and circulating tumor DNA in adult patients with newly diagnosed glioblastoma
title Imaging and histopathologic correlates of plasma cell-free DNA concentration and circulating tumor DNA in adult patients with newly diagnosed glioblastoma
title_full Imaging and histopathologic correlates of plasma cell-free DNA concentration and circulating tumor DNA in adult patients with newly diagnosed glioblastoma
title_fullStr Imaging and histopathologic correlates of plasma cell-free DNA concentration and circulating tumor DNA in adult patients with newly diagnosed glioblastoma
title_full_unstemmed Imaging and histopathologic correlates of plasma cell-free DNA concentration and circulating tumor DNA in adult patients with newly diagnosed glioblastoma
title_short Imaging and histopathologic correlates of plasma cell-free DNA concentration and circulating tumor DNA in adult patients with newly diagnosed glioblastoma
title_sort imaging and histopathologic correlates of plasma cell-free dna concentration and circulating tumor dna in adult patients with newly diagnosed glioblastoma
topic Clinical Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7045782/
https://www.ncbi.nlm.nih.gov/pubmed/32140683
http://dx.doi.org/10.1093/noajnl/vdaa016
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