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MGMT methylation may benefit overall survival in patients with moderately vascularized glioblastomas
OBJECTIVES: To assess the combined role of tumor vascularity, estimated from perfusion MRI, and MGMT methylation status on overall survival (OS) in patients with glioblastoma. METHODS: A multicentric international dataset including 96 patients from NCT03439332 clinical study were used to study the p...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7880975/ https://www.ncbi.nlm.nih.gov/pubmed/33001310 http://dx.doi.org/10.1007/s00330-020-07297-4 |
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author | Fuster-Garcia, Elies Lorente Estellés, David Álvarez-Torres, María del Mar Juan-Albarracín, Javier Chelebian, Eduard Rovira, Alex Acosta, Cristina Auger Pineda, Jose Oleaga, Laura Mollá-Olmos, Enrique Filice, Silvano Due-Tønnessen, Paulina Meling, Torstein R. Emblem, Kyrre E. García-Gómez, Juan M. |
author_facet | Fuster-Garcia, Elies Lorente Estellés, David Álvarez-Torres, María del Mar Juan-Albarracín, Javier Chelebian, Eduard Rovira, Alex Acosta, Cristina Auger Pineda, Jose Oleaga, Laura Mollá-Olmos, Enrique Filice, Silvano Due-Tønnessen, Paulina Meling, Torstein R. Emblem, Kyrre E. García-Gómez, Juan M. |
author_sort | Fuster-Garcia, Elies |
collection | PubMed |
description | OBJECTIVES: To assess the combined role of tumor vascularity, estimated from perfusion MRI, and MGMT methylation status on overall survival (OS) in patients with glioblastoma. METHODS: A multicentric international dataset including 96 patients from NCT03439332 clinical study were used to study the prognostic relationships between MGMT and perfusion markers. Relative cerebral blood volume (rCBV) in the most vascularized tumor regions was automatically obtained from preoperative MRIs using ONCOhabitats online analysis service. Cox survival regression models and stratification strategies were conducted to define a subpopulation that is particularly favored by MGMT methylation in terms of OS. RESULTS: rCBV distributions did not differ significantly (p > 0.05) in the methylated and the non-methylated subpopulations. In patients with moderately vascularized tumors (rCBV < 10.73), MGMT methylation was a positive predictive factor for OS (HR = 2.73, p = 0.003, AUC = 0.70). In patients with highly vascularized tumors (rCBV > 10.73), however, there was no significant effect of MGMT methylation (HR = 1.72, p = 0.10, AUC = 0.56). CONCLUSIONS: Our results indicate the existence of complementary prognostic information provided by MGMT methylation and rCBV. Perfusion markers could identify a subpopulation of patients who will benefit the most from MGMT methylation. Not considering this information may lead to bias in the interpretation of clinical studies. KEY POINTS: • MRI perfusion provides complementary prognostic information to MGMT methylation. • MGMT methylation improves prognosis in glioblastoma patients with moderate vascular profile. • Failure to consider these relations may lead to bias in the interpretation of clinical studies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00330-020-07297-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7880975 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-78809752021-02-18 MGMT methylation may benefit overall survival in patients with moderately vascularized glioblastomas Fuster-Garcia, Elies Lorente Estellés, David Álvarez-Torres, María del Mar Juan-Albarracín, Javier Chelebian, Eduard Rovira, Alex Acosta, Cristina Auger Pineda, Jose Oleaga, Laura Mollá-Olmos, Enrique Filice, Silvano Due-Tønnessen, Paulina Meling, Torstein R. Emblem, Kyrre E. García-Gómez, Juan M. Eur Radiol Oncology OBJECTIVES: To assess the combined role of tumor vascularity, estimated from perfusion MRI, and MGMT methylation status on overall survival (OS) in patients with glioblastoma. METHODS: A multicentric international dataset including 96 patients from NCT03439332 clinical study were used to study the prognostic relationships between MGMT and perfusion markers. Relative cerebral blood volume (rCBV) in the most vascularized tumor regions was automatically obtained from preoperative MRIs using ONCOhabitats online analysis service. Cox survival regression models and stratification strategies were conducted to define a subpopulation that is particularly favored by MGMT methylation in terms of OS. RESULTS: rCBV distributions did not differ significantly (p > 0.05) in the methylated and the non-methylated subpopulations. In patients with moderately vascularized tumors (rCBV < 10.73), MGMT methylation was a positive predictive factor for OS (HR = 2.73, p = 0.003, AUC = 0.70). In patients with highly vascularized tumors (rCBV > 10.73), however, there was no significant effect of MGMT methylation (HR = 1.72, p = 0.10, AUC = 0.56). CONCLUSIONS: Our results indicate the existence of complementary prognostic information provided by MGMT methylation and rCBV. Perfusion markers could identify a subpopulation of patients who will benefit the most from MGMT methylation. Not considering this information may lead to bias in the interpretation of clinical studies. KEY POINTS: • MRI perfusion provides complementary prognostic information to MGMT methylation. • MGMT methylation improves prognosis in glioblastoma patients with moderate vascular profile. • Failure to consider these relations may lead to bias in the interpretation of clinical studies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00330-020-07297-4) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-10-01 2021 /pmc/articles/PMC7880975/ /pubmed/33001310 http://dx.doi.org/10.1007/s00330-020-07297-4 Text en © The Author(s) 2020 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Oncology Fuster-Garcia, Elies Lorente Estellés, David Álvarez-Torres, María del Mar Juan-Albarracín, Javier Chelebian, Eduard Rovira, Alex Acosta, Cristina Auger Pineda, Jose Oleaga, Laura Mollá-Olmos, Enrique Filice, Silvano Due-Tønnessen, Paulina Meling, Torstein R. Emblem, Kyrre E. García-Gómez, Juan M. MGMT methylation may benefit overall survival in patients with moderately vascularized glioblastomas |
title | MGMT methylation may benefit overall survival in patients with moderately vascularized glioblastomas |
title_full | MGMT methylation may benefit overall survival in patients with moderately vascularized glioblastomas |
title_fullStr | MGMT methylation may benefit overall survival in patients with moderately vascularized glioblastomas |
title_full_unstemmed | MGMT methylation may benefit overall survival in patients with moderately vascularized glioblastomas |
title_short | MGMT methylation may benefit overall survival in patients with moderately vascularized glioblastomas |
title_sort | mgmt methylation may benefit overall survival in patients with moderately vascularized glioblastomas |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7880975/ https://www.ncbi.nlm.nih.gov/pubmed/33001310 http://dx.doi.org/10.1007/s00330-020-07297-4 |
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