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Neutrophil-to-lymphocyte ratio, Factor VIII and Antithrombin III: inflammatory-clotting biomarkers in glioma

One of the key difficulties in glioma treatment is our limited ability to consistently assess cancer response or progression either by neuroimaging or specific blood biomarkers. An ideal biomarker could be measured through non-invasive methods such as blood-based biomarkers, aiding both early diagno...

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Autores principales: Koudriavtseva, Tatiana, Villani, Veronica, Lorenzano, Svetlana, Giannarelli, Diana, Di Domenico, Enea Gino, Stefanile, Annunziata, Maschio, Marta, D'Agosto, Giovanna, Pimpinelli, Fulvia, Tanzilli, Antonio, Galiè, Edvina, Pace, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Leibniz Research Centre for Working Environment and Human Factors 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8326499/
https://www.ncbi.nlm.nih.gov/pubmed/34345234
http://dx.doi.org/10.17179/excli2021-3831
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author Koudriavtseva, Tatiana
Villani, Veronica
Lorenzano, Svetlana
Giannarelli, Diana
Di Domenico, Enea Gino
Stefanile, Annunziata
Maschio, Marta
D'Agosto, Giovanna
Pimpinelli, Fulvia
Tanzilli, Antonio
Galiè, Edvina
Pace, Andrea
author_facet Koudriavtseva, Tatiana
Villani, Veronica
Lorenzano, Svetlana
Giannarelli, Diana
Di Domenico, Enea Gino
Stefanile, Annunziata
Maschio, Marta
D'Agosto, Giovanna
Pimpinelli, Fulvia
Tanzilli, Antonio
Galiè, Edvina
Pace, Andrea
author_sort Koudriavtseva, Tatiana
collection PubMed
description One of the key difficulties in glioma treatment is our limited ability to consistently assess cancer response or progression either by neuroimaging or specific blood biomarkers. An ideal biomarker could be measured through non-invasive methods such as blood-based biomarkers, aiding both early diagnosis and monitoring disease evolution. This is a single-center, case-control, 10-year retrospective, longitudinal study. We evaluated routine coagulation factors in 138 glioma patients (45 Females/93 Males; median [range] age, 56.4 [27-82] years; 64 non-recurrent/74 recurrent) and, for comparison, in 56 relapsing-remitting MS patients (41 Females/15 Males; 40.8 [25-62] years, 35 stable/21 active) and 23 controls (16 Females/7 Males; 41.7 [24-62] years) as well as Neutrophil-to-lymphocyte ratio (NLR) in subgroups of 127 glioma patients, 33 MS patients and 23 healthy controls. Secondly, we assessed whether these indicators could be predictive of overall (OS) and progression-free survival (PFS) in glioma patients. NLR, d-dimer, Antithrombin III and Factor VIII were significantly higher in glioma patients compared to both MS patients and controls (p<0.0001 for all). ROC curves confirmed that either NLR, Antithrombin III or Factor VIII were moderately accurate biomarkers (0.7<AUC<0.9) for glioma patients compared to other two groups whereas d-dimer was a moderately accurate marker for glioma only when compared to controls. In multivariable analysis, NLR ≥ 4.3 (median) (HR 1.53 [95 % CI 1.04-2.26], p=0.03) together with the Karnofsky Performance Status (KPS) ≥ 80 (median) (0.46 [0.31-0.69], p<0.0001) and use of steroids (1.75 [1.19-2.57], p=0.004) resulted independent predictors of OS while only KPS was independently associated with PFS. Our study showed increased levels of either NLR, Antithrombin III, Factor VIII, or d-dimer in glioma patients compared to MS patients and controls, where the first three represented moderately accurate biomarkers for this cancer. Among these markers, only NLR was found to be predictive for OS along with severe disability and steroid therapy.
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spelling pubmed-83264992021-08-02 Neutrophil-to-lymphocyte ratio, Factor VIII and Antithrombin III: inflammatory-clotting biomarkers in glioma Koudriavtseva, Tatiana Villani, Veronica Lorenzano, Svetlana Giannarelli, Diana Di Domenico, Enea Gino Stefanile, Annunziata Maschio, Marta D'Agosto, Giovanna Pimpinelli, Fulvia Tanzilli, Antonio Galiè, Edvina Pace, Andrea EXCLI J Original Article One of the key difficulties in glioma treatment is our limited ability to consistently assess cancer response or progression either by neuroimaging or specific blood biomarkers. An ideal biomarker could be measured through non-invasive methods such as blood-based biomarkers, aiding both early diagnosis and monitoring disease evolution. This is a single-center, case-control, 10-year retrospective, longitudinal study. We evaluated routine coagulation factors in 138 glioma patients (45 Females/93 Males; median [range] age, 56.4 [27-82] years; 64 non-recurrent/74 recurrent) and, for comparison, in 56 relapsing-remitting MS patients (41 Females/15 Males; 40.8 [25-62] years, 35 stable/21 active) and 23 controls (16 Females/7 Males; 41.7 [24-62] years) as well as Neutrophil-to-lymphocyte ratio (NLR) in subgroups of 127 glioma patients, 33 MS patients and 23 healthy controls. Secondly, we assessed whether these indicators could be predictive of overall (OS) and progression-free survival (PFS) in glioma patients. NLR, d-dimer, Antithrombin III and Factor VIII were significantly higher in glioma patients compared to both MS patients and controls (p<0.0001 for all). ROC curves confirmed that either NLR, Antithrombin III or Factor VIII were moderately accurate biomarkers (0.7<AUC<0.9) for glioma patients compared to other two groups whereas d-dimer was a moderately accurate marker for glioma only when compared to controls. In multivariable analysis, NLR ≥ 4.3 (median) (HR 1.53 [95 % CI 1.04-2.26], p=0.03) together with the Karnofsky Performance Status (KPS) ≥ 80 (median) (0.46 [0.31-0.69], p<0.0001) and use of steroids (1.75 [1.19-2.57], p=0.004) resulted independent predictors of OS while only KPS was independently associated with PFS. Our study showed increased levels of either NLR, Antithrombin III, Factor VIII, or d-dimer in glioma patients compared to MS patients and controls, where the first three represented moderately accurate biomarkers for this cancer. Among these markers, only NLR was found to be predictive for OS along with severe disability and steroid therapy. Leibniz Research Centre for Working Environment and Human Factors 2021-07-08 /pmc/articles/PMC8326499/ /pubmed/34345234 http://dx.doi.org/10.17179/excli2021-3831 Text en Copyright © 2021 Koudriavtseva et al. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ) You are free to copy, distribute and transmit the work, provided the original author and source are credited.
spellingShingle Original Article
Koudriavtseva, Tatiana
Villani, Veronica
Lorenzano, Svetlana
Giannarelli, Diana
Di Domenico, Enea Gino
Stefanile, Annunziata
Maschio, Marta
D'Agosto, Giovanna
Pimpinelli, Fulvia
Tanzilli, Antonio
Galiè, Edvina
Pace, Andrea
Neutrophil-to-lymphocyte ratio, Factor VIII and Antithrombin III: inflammatory-clotting biomarkers in glioma
title Neutrophil-to-lymphocyte ratio, Factor VIII and Antithrombin III: inflammatory-clotting biomarkers in glioma
title_full Neutrophil-to-lymphocyte ratio, Factor VIII and Antithrombin III: inflammatory-clotting biomarkers in glioma
title_fullStr Neutrophil-to-lymphocyte ratio, Factor VIII and Antithrombin III: inflammatory-clotting biomarkers in glioma
title_full_unstemmed Neutrophil-to-lymphocyte ratio, Factor VIII and Antithrombin III: inflammatory-clotting biomarkers in glioma
title_short Neutrophil-to-lymphocyte ratio, Factor VIII and Antithrombin III: inflammatory-clotting biomarkers in glioma
title_sort neutrophil-to-lymphocyte ratio, factor viii and antithrombin iii: inflammatory-clotting biomarkers in glioma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8326499/
https://www.ncbi.nlm.nih.gov/pubmed/34345234
http://dx.doi.org/10.17179/excli2021-3831
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