Diffuse Astrocytoma, IDH-Wildtype: A Dissolving Diagnosis. Issue 6 (9th February 2018)
- Record Type:
- Journal Article
- Title:
- Diffuse Astrocytoma, IDH-Wildtype: A Dissolving Diagnosis. Issue 6 (9th February 2018)
- Main Title:
- Diffuse Astrocytoma, IDH-Wildtype: A Dissolving Diagnosis
- Authors:
- Hasselblatt, Martin
Jaber, Mohammed
Reuss, David
Grauer, Oliver
Bibo, Annkatrin
Terwey, Stephanie
Schick, Uta
Ebel, Heinrich
Niederstadt, Thomas
Stummer, Walter
von Deimling, Andreas
Paulus, Werner - Abstract:
- Abstract: The histological and molecular features and even the mere existence of diffuse astrocytoma, IDH-wildtype, remain unclear. We therefore examined 212 diffuse astrocytomas (grade II WHO) in adults using IDH1(R132H) immunohistochemistry followed by IDH1/IDH2 sequencing and neuroimaging review. DNA methylation status and copy number profiles were assessed by Infinium HumanMethylation450k BeadChip. Only 25/212 patients harbored tumors without IDH1/IDH2 hotspot mutations and without contrast enhancement. By DNA methylation profiling, 10/25 tumors were classified as glioblastoma, IDH-wildtype, and an additional 7 cases could not be classified using methylome analysis, but showed genetic characteristics of glioblastoma. Histologically, all of these 17 tumors were low-grade diffuse astrocytomas. Nevertheless, 10/17 patients experienced early malignant progression. Other methylation classes included diffuse midline glioma, H3 K27M-mutant, diffuse astrocytoma, IDH-mutant, pilocytic astrocytoma, and normal or reactive brain tissue (total n = 8). In conclusion, no convincing diffuse astrocytoma, IDH-wildtype, was identified. Most IDH-wildtype tumors showing histopathological and radiological features of low-grade diffuse astrocytoma exhibit molecular and clinical features of high-grade glioma and may represent an early stage of primary glioblastoma. Our findings have implications for the biology, classification and neuropathological diagnosis of diffuse astrocytoma, IDH-wildtypeAbstract: The histological and molecular features and even the mere existence of diffuse astrocytoma, IDH-wildtype, remain unclear. We therefore examined 212 diffuse astrocytomas (grade II WHO) in adults using IDH1(R132H) immunohistochemistry followed by IDH1/IDH2 sequencing and neuroimaging review. DNA methylation status and copy number profiles were assessed by Infinium HumanMethylation450k BeadChip. Only 25/212 patients harbored tumors without IDH1/IDH2 hotspot mutations and without contrast enhancement. By DNA methylation profiling, 10/25 tumors were classified as glioblastoma, IDH-wildtype, and an additional 7 cases could not be classified using methylome analysis, but showed genetic characteristics of glioblastoma. Histologically, all of these 17 tumors were low-grade diffuse astrocytomas. Nevertheless, 10/17 patients experienced early malignant progression. Other methylation classes included diffuse midline glioma, H3 K27M-mutant, diffuse astrocytoma, IDH-mutant, pilocytic astrocytoma, and normal or reactive brain tissue (total n = 8). In conclusion, no convincing diffuse astrocytoma, IDH-wildtype, was identified. Most IDH-wildtype tumors showing histopathological and radiological features of low-grade diffuse astrocytoma exhibit molecular and clinical features of high-grade glioma and may represent an early stage of primary glioblastoma. Our findings have implications for the biology, classification and neuropathological diagnosis of diffuse astrocytoma, IDH-wildtype in adults. … (more)
- Is Part Of:
- Journal of neuropathology and experimental neurology. Volume 77:Issue 6(2018)
- Journal:
- Journal of neuropathology and experimental neurology
- Issue:
- Volume 77:Issue 6(2018)
- Issue Display:
- Volume 77, Issue 6 (2018)
- Year:
- 2018
- Volume:
- 77
- Issue:
- 6
- Issue Sort Value:
- 2018-0077-0006-0000
- Page Start:
- 422
- Page End:
- 425
- Publication Date:
- 2018-02-09
- Subjects:
- Adult -- Diffuse astrocytoma -- DNA methylation profiling -- Glioblastoma -- Isocitrate dehydrogenase -- Outcome
Neurology -- Diseases -- Periodicals
Neurology -- Diseases -- Physiopathology -- Periodicals
616.8047 - Journal URLs:
- http://journals.lww.com/jneuropath/pages/default.aspx ↗
http://jnen.oxfordjournals.org/ ↗
http://journals.lww.com ↗ - DOI:
- 10.1093/jnen/nly012 ↗
- Languages:
- English
- ISSNs:
- 0022-3069
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5021.700000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 12198.xml