Significance of complete 1p/19q co-deletion, IDH1 mutation and MGMT promoter methylation in gliomas: use with caution

The histopathological diagnosis of diffuse gliomas often lacks the precision that is needed for tailored treatment of individual patients. Assessment of the molecular aberrations will probably allow more robust and prognostically relevant classification of these tumors. Markers that have gained a lo...

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Published inModern pathology Vol. 26; no. 7; pp. 922 - 929
Main Authors Boots-Sprenger, Sandra H E, Sijben, Angelique, Rijntjes, Jos, Tops, Bastiaan B J, Idema, Albert J, Rivera, Andreana L, Bleeker, Fonnet E, Gijtenbeek, Anja M, Diefes, Kristin, Heathcock, Lindsey, Aldape, Kenneth D, Jeuken, Judith W M, Wesseling, Pieter
Format Journal Article
LanguageEnglish
Published New York Nature Publishing Group US 01.07.2013
Elsevier Limited
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Abstract The histopathological diagnosis of diffuse gliomas often lacks the precision that is needed for tailored treatment of individual patients. Assessment of the molecular aberrations will probably allow more robust and prognostically relevant classification of these tumors. Markers that have gained a lot of interest in this respect are co-deletion of complete chromosome arms 1p and 19q, (hyper)methylation of the MGMT promoter and IDH1 mutations. The aim of this study was to assess the prognostic significance of complete 1p/19q co-deletion, MGMT promoter methylation and IDH1 mutations in patients suffering from diffuse gliomas. The presence of these molecular aberrations was investigated in a series of 561 diffuse astrocytic and oligodendroglial tumors (low grade n =110, anaplastic n =118 and glioblastoma n =333) and correlated with age at diagnosis and overall survival. Complete 1p/19q co-deletion, MGMT promoter methylation and/or IDH1 mutation generally signified a better prognosis for patients with a diffuse glioma including glioblastoma. However, in all 10 patients with a histopathological diagnosis of glioblastoma included in this study complete 1p/19q co-deletion was not associated with improved survival. Furthermore, in glioblastoma patients >50 years of age the favorable prognostic significance of IDH1 mutation and MGMT promoter methylation was absent. In conclusion, molecular diagnostics is a powerful tool to obtain prognostically relevant information for glioma patients. However, for individual patients the molecular information should be interpreted with caution and weighed in the context of parameters such as age and histopathological diagnosis.
AbstractList The histopathological diagnosis of diffuse gliomas often lacks the precision that is needed for tailored treatment of individual patients. Assessment of the molecular aberrations will probably allow more robust and prognostically relevant classification of these tumors. Markers that have gained a lot of interest in this respect are co-deletion of complete chromosome arms 1p and 19q, (hyper)methylation of the MGMT promoter and IDH1 mutations. The aim of this study was to assess the prognostic significance of complete 1p/19q co-deletion, MGMT promoter methylation and IDH1 mutations in patients suffering from diffuse gliomas. The presence of these molecular aberrations was investigated in a series of 561 diffuse astrocytic and oligodendroglial tumors (low grade n=110, anaplastic n=118 and glioblastoma n=333) and correlated with age at diagnosis and overall survival. Complete 1p/19q co-deletion, MGMT promoter methylation and/or IDH1 mutation generally signified a better prognosis for patients with a diffuse glioma including glioblastoma. However, in all 10 patients with a histopathological diagnosis of glioblastoma included in this study complete 1p/19q co-deletion was not associated with improved survival. Furthermore, in glioblastoma patients >50 years of age the favorable prognostic significance of IDH1 mutation and MGMT promoter methylation was absent. In conclusion, molecular diagnostics is a powerful tool to obtain prognostically relevant information for glioma patients. However, for individual patients the molecular information should be interpreted with caution and weighed in the context of parameters such as age and histopathological diagnosis.
The histopathological diagnosis of diffuse gliomas often lacks the precision that is needed for tailored treatment of individual patients. Assessment of the molecular aberrations will probably allow more robust and prognostically relevant classification of these tumors. Markers that have gained a lot of interest in this respect are co-deletion of complete chromosome arms 1p and 19q, (hyper)methylation of the MGMT promoter and IDH1 mutations. The aim of this study was to assess the prognostic significance of complete 1p/19q co-deletion, MGMT promoter methylation and IDH1 mutations in patients suffering from diffuse gliomas. The presence of these molecular aberrations was investigated in a series of 561 diffuse astrocytic and oligodendroglial tumors (low grade n =110, anaplastic n =118 and glioblastoma n =333) and correlated with age at diagnosis and overall survival. Complete 1p/19q co-deletion, MGMT promoter methylation and/or IDH1 mutation generally signified a better prognosis for patients with a diffuse glioma including glioblastoma. However, in all 10 patients with a histopathological diagnosis of glioblastoma included in this study complete 1p/19q co-deletion was not associated with improved survival. Furthermore, in glioblastoma patients >50 years of age the favorable prognostic significance of IDH1 mutation and MGMT promoter methylation was absent. In conclusion, molecular diagnostics is a powerful tool to obtain prognostically relevant information for glioma patients. However, for individual patients the molecular information should be interpreted with caution and weighed in the context of parameters such as age and histopathological diagnosis.
Author Wesseling, Pieter
Bleeker, Fonnet E
Sijben, Angelique
Idema, Albert J
Boots-Sprenger, Sandra H E
Aldape, Kenneth D
Jeuken, Judith W M
Heathcock, Lindsey
Diefes, Kristin
Tops, Bastiaan B J
Gijtenbeek, Anja M
Rivera, Andreana L
Rijntjes, Jos
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  organization: Department of Pathology, Radboud University Nijmegen Medical Centre (RUNMC)
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  surname: Tops
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  organization: Department of Pathology, Radboud University Nijmegen Medical Centre (RUNMC)
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  organization: Department of Neurosurgery, RUNMC
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  organization: The University of Texas, MD Anderson Cancer Center, Department of Pathology and Genomic Medicine, The Methodist Hospital Houston
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  surname: Diefes
  fullname: Diefes, Kristin
  organization: The University of Texas, MD Anderson Cancer Center, Department of Pathology and Genomic Medicine, The Methodist Hospital Houston
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  organization: Department of Pathology and Genomic Medicine, The Methodist Hospital Houston
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  organization: The University of Texas, MD Anderson Cancer Center
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  fullname: Wesseling, Pieter
  organization: Department of Pathology, Radboud University Nijmegen Medical Centre (RUNMC), Department of Pathology, Canisius Wilhelmina Hospital, Department of Pathology, VU University Medical Center
BackLink https://www.ncbi.nlm.nih.gov/pubmed/23429602$$D View this record in MEDLINE/PubMed
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molecular markers
complete 1p/19q co-deletion
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Snippet The histopathological diagnosis of diffuse gliomas often lacks the precision that is needed for tailored treatment of individual patients. Assessment of the...
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SubjectTerms 692/53/2422
692/699/67/1922
692/700/139/422
Adult
Age
Biomarkers, Tumor - genetics
Brain cancer
Brain Neoplasms - classification
Brain Neoplasms - genetics
Brain Neoplasms - mortality
Chromosome Deletion
Chromosomes, Human, Pair 1 - genetics
Chromosomes, Human, Pair 19 - genetics
DNA Methylation
DNA Modification Methylases - genetics
DNA Repair Enzymes - genetics
Female
Gene Deletion
Glioma - classification
Glioma - genetics
Glioma - mortality
Hospitals
Humans
Isocitrate Dehydrogenase - genetics
Kaplan-Meier Estimate
Laboratory Medicine
Male
Medical prognosis
Medicine
Medicine & Public Health
Middle Aged
Mutation
Nervous system
Neurology
original-article
Pathology
Pathology, Molecular
Patients
Prognosis
Promoter Regions, Genetic
Tumor Suppressor Proteins - genetics
Tumors
Title Significance of complete 1p/19q co-deletion, IDH1 mutation and MGMT promoter methylation in gliomas: use with caution
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Volume 26
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