Genetically Defined Oligodendroglioma Is Characterized by Indistinct Tumor Borders at MRI

In 2016, the World Health Organization revised the brain tumor classification, making mutation and 1p/19q codeletion the defining features of oligodendroglioma. To determine whether imaging characteristics previously associated with oligodendroglial tumors are still applicable, we evaluated the MR i...

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Published inAmerican journal of neuroradiology : AJNR Vol. 38; no. 4; pp. 678 - 684
Main Authors Johnson, D.R., Diehn, F.E., Giannini, C., Jenkins, R.B., Jenkins, S.M., Parney, I.F., Kaufmann, T.J.
Format Journal Article
LanguageEnglish
Published United States American Society of Neuroradiology 01.04.2017
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Online AccessGet full text
ISSN0195-6108
1936-959X
DOI10.3174/ajnr.A5070

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Abstract In 2016, the World Health Organization revised the brain tumor classification, making mutation and 1p/19q codeletion the defining features of oligodendroglioma. To determine whether imaging characteristics previously associated with oligodendroglial tumors are still applicable, we evaluated the MR imaging features of genetically defined oligodendrogliomas. One hundred forty-eight adult patients with untreated World Health Organization grade II and III infiltrating gliomas with histologic oligodendroglial morphology, known 1p/19q status, and at least 1 preoperative MR imaging were retrospectively identified. The association of 1p/19q codeletion with tumor imaging characteristics and ADC values was evaluated. Ninety of 148 (61%) patients had 1p/19q codeleted tumors, corresponding to genetically defined oligodendroglioma, and 58/148 (39%) did not show 1p/19q codeletion, corresponding to astrocytic tumors. Eighty-three of 90 (92%) genetically defined oligodendrogliomas had noncircumscribed borders, compared with 26/58 (45%) non-1p/19q codeleted tumors with at least partial histologic oligodendroglial morphology ( < .0001). Eighty-nine of 90 (99%) oligodendrogliomas were heterogeneous on T1- and/or T2-weighted imaging. In patients with available ADC values, a lower mean ADC value predicted 1p/19q codeletion ( = .0005). Imaging characteristics of World Health Organization 2016 genetically defined oligodendrogliomas differ from the previously considered characteristics of morphologically defined oligodendrogliomas. We found that genetically defined oligodendrogliomas were commonly poorly circumscribed and were almost always heterogeneous in signal intensity.
AbstractList The authors wanted to determine whether imaging characteristics previously associated with oligodendroglial tumors were still applicable given the 2016 WHO classification that made IDH mutation and 1p/19q codeletion the defining features of oligodendroglioma. They found that 92% of genetically defined oligodendrogliomas had noncircumscribed borders, compared with 45% of non-1p/19q codeleted tumors with at least partial histologic oligodendroglial morphology. Ninety-nine percent of oligodendrogliomas were heterogeneous on T1- and/or T2-weighted imaging.BACKGROUND AND PURPOSE:In 2016, the World Health Organization revised the brain tumor classification, making IDH mutation and 1p/19q codeletion the defining features of oligodendroglioma. To determine whether imaging characteristics previously associated with oligodendroglial tumors are still applicable, we evaluated the MR imaging features of genetically defined oligodendrogliomas.MATERIALS AND METHODS:One hundred forty-eight adult patients with untreated World Health Organization grade II and III infiltrating gliomas with histologic oligodendroglial morphology, known 1p/19q status, and at least 1 preoperative MR imaging were retrospectively identified. The association of 1p/19q codeletion with tumor imaging characteristics and ADC values was evaluated.RESULTS:Ninety of 148 (61%) patients had 1p/19q codeleted tumors, corresponding to genetically defined oligodendroglioma, and 58/148 (39%) did not show 1p/19q codeletion, corresponding to astrocytic tumors. Eighty-three of 90 (92%) genetically defined oligodendrogliomas had noncircumscribed borders, compared with 26/58 (45%) non-1p/19q codeleted tumors with at least partial histologic oligodendroglial morphology (P < .0001). Eighty-nine of 90 (99%) oligodendrogliomas were heterogeneous on T1- and/or T2-weighted imaging. In patients with available ADC values, a lower mean ADC value predicted 1p/19q codeletion (P = .0005).CONCLUSIONS:Imaging characteristics of World Health Organization 2016 genetically defined oligodendrogliomas differ from the previously considered characteristics of morphologically defined oligodendrogliomas. We found that genetically defined oligodendrogliomas were commonly poorly circumscribed and were almost always heterogeneous in signal intensity.
The authors wanted to determine whether imaging characteristics previously associated with oligodendroglial tumors were still applicable given the 2016 WHO classification that made IDH mutation and 1p/19q codeletion the defining features of oligodendroglioma. They found that 92% of genetically defined oligodendrogliomas had noncircumscribed borders, compared with 45% of non-1p/19q codeleted tumors with at least partial histologic oligodendroglial morphology. Ninety-nine percent of oligodendrogliomas were heterogeneous on T1- and/or T2-weighted imaging.
BACKGROUND AND PURPOSEIn 2016, the World Health Organization revised the brain tumor classification, making IDH mutation and 1p/19q codeletion the defining features of oligodendroglioma. To determine whether imaging characteristics previously associated with oligodendroglial tumors are still applicable, we evaluated the MR imaging features of genetically defined oligodendrogliomas.MATERIALS AND METHODSOne hundred forty-eight adult patients with untreated World Health Organization grade II and III infiltrating gliomas with histologic oligodendroglial morphology, known 1p/19q status, and at least 1 preoperative MR imaging were retrospectively identified. The association of 1p/19q codeletion with tumor imaging characteristics and ADC values was evaluated.RESULTSNinety of 148 (61%) patients had 1p/19q codeleted tumors, corresponding to genetically defined oligodendroglioma, and 58/148 (39%) did not show 1p/19q codeletion, corresponding to astrocytic tumors. Eighty-three of 90 (92%) genetically defined oligodendrogliomas had noncircumscribed borders, compared with 26/58 (45%) non-1p/19q codeleted tumors with at least partial histologic oligodendroglial morphology (P < .0001). Eighty-nine of 90 (99%) oligodendrogliomas were heterogeneous on T1- and/or T2-weighted imaging. In patients with available ADC values, a lower mean ADC value predicted 1p/19q codeletion (P = .0005).CONCLUSIONSImaging characteristics of World Health Organization 2016 genetically defined oligodendrogliomas differ from the previously considered characteristics of morphologically defined oligodendrogliomas. We found that genetically defined oligodendrogliomas were commonly poorly circumscribed and were almost always heterogeneous in signal intensity.
In 2016, the World Health Organization revised the brain tumor classification, making mutation and 1p/19q codeletion the defining features of oligodendroglioma. To determine whether imaging characteristics previously associated with oligodendroglial tumors are still applicable, we evaluated the MR imaging features of genetically defined oligodendrogliomas. One hundred forty-eight adult patients with untreated World Health Organization grade II and III infiltrating gliomas with histologic oligodendroglial morphology, known 1p/19q status, and at least 1 preoperative MR imaging were retrospectively identified. The association of 1p/19q codeletion with tumor imaging characteristics and ADC values was evaluated. Ninety of 148 (61%) patients had 1p/19q codeleted tumors, corresponding to genetically defined oligodendroglioma, and 58/148 (39%) did not show 1p/19q codeletion, corresponding to astrocytic tumors. Eighty-three of 90 (92%) genetically defined oligodendrogliomas had noncircumscribed borders, compared with 26/58 (45%) non-1p/19q codeleted tumors with at least partial histologic oligodendroglial morphology ( < .0001). Eighty-nine of 90 (99%) oligodendrogliomas were heterogeneous on T1- and/or T2-weighted imaging. In patients with available ADC values, a lower mean ADC value predicted 1p/19q codeletion ( = .0005). Imaging characteristics of World Health Organization 2016 genetically defined oligodendrogliomas differ from the previously considered characteristics of morphologically defined oligodendrogliomas. We found that genetically defined oligodendrogliomas were commonly poorly circumscribed and were almost always heterogeneous in signal intensity.
Author Johnson, D.R.
Diehn, F.E.
Jenkins, R.B.
Parney, I.F.
Giannini, C.
Jenkins, S.M.
Kaufmann, T.J.
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Cites_doi 10.1016/S0002-9440(10)64183-1
10.1158/1078-0432.CCR-04-0209
10.1002/jmri.21062
10.1007/s11912-012-0281-5
10.1007/s00401-016-1545-1
10.1158/1078-0432.CCR-04-0681
10.1056/NEJMoa1407279
10.1038/ng.2388
10.1093/brain/awl108
10.1093/neuonc/nor122
10.1056/NEJMoa1500925
10.1158/1078-0432.CCR-07-1964
10.1093/neuonc/nos259
10.1200/JCO.2000.18.3.636
10.3174/ajnr.A3384
10.1093/neuonc/nov307
10.1172/JCI67229
10.1200/JCO.2013.49.3726
10.1126/scitranslmed.3002693
10.1200/JCO.2012.43.2229
10.1136/jnnp.2009.178806
10.3892/ol.2014.2013
10.1212/01.WNL.0000148642.26985.68
10.3174/ajnr.A3352
10.1038/srep16238
10.1007/s10014-016-0249-5
10.1007/s00330-015-4025-4
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References 2018022808151318000_38.4.678.9
2018022808151318000_38.4.678.29
2018022808151318000_38.4.678.2
2018022808151318000_38.4.678.25
2018022808151318000_38.4.678.1
2018022808151318000_38.4.678.26
2018022808151318000_38.4.678.27
2018022808151318000_38.4.678.3
2018022808151318000_38.4.678.28
2018022808151318000_38.4.678.6
2018022808151318000_38.4.678.21
2018022808151318000_38.4.678.5
2018022808151318000_38.4.678.22
2018022808151318000_38.4.678.8
2018022808151318000_38.4.678.23
2018022808151318000_38.4.678.7
2018022808151318000_38.4.678.24
Smith (2018022808151318000_38.4.678.4) 2000; 18
2018022808151318000_38.4.678.20
2018022808151318000_38.4.678.18
2018022808151318000_38.4.678.19
2018022808151318000_38.4.678.14
2018022808151318000_38.4.678.15
2018022808151318000_38.4.678.16
2018022808151318000_38.4.678.17
2018022808151318000_38.4.678.10
2018022808151318000_38.4.678.12
2018022808151318000_38.4.678.13
2018022808151318000_38.4.678.30
Zlatescu (2018022808151318000_38.4.678.11) 2001; 61
References_xml – ident: 2018022808151318000_38.4.678.8
– ident: 2018022808151318000_38.4.678.19
  doi: 10.1016/S0002-9440(10)64183-1
– ident: 2018022808151318000_38.4.678.13
  doi: 10.1158/1078-0432.CCR-04-0209
– ident: 2018022808151318000_38.4.678.16
  doi: 10.1002/jmri.21062
– ident: 2018022808151318000_38.4.678.5
  doi: 10.1007/s11912-012-0281-5
– ident: 2018022808151318000_38.4.678.6
  doi: 10.1007/s00401-016-1545-1
– ident: 2018022808151318000_38.4.678.14
  doi: 10.1158/1078-0432.CCR-04-0681
– ident: 2018022808151318000_38.4.678.7
  doi: 10.1056/NEJMoa1407279
– ident: 2018022808151318000_38.4.678.10
  doi: 10.1038/ng.2388
– ident: 2018022808151318000_38.4.678.15
  doi: 10.1093/brain/awl108
– ident: 2018022808151318000_38.4.678.30
  doi: 10.1093/neuonc/nor122
– ident: 2018022808151318000_38.4.678.1
  doi: 10.1056/NEJMoa1500925
– ident: 2018022808151318000_38.4.678.17
  doi: 10.1158/1078-0432.CCR-07-1964
– ident: 2018022808151318000_38.4.678.26
  doi: 10.1093/neuonc/nos259
– volume: 18
  start-page: 636
  year: 2000
  ident: 2018022808151318000_38.4.678.4
  article-title: Alterations of chromosome arms 1p and 19q as predictors of survival in oligodendrogliomas, astrocytomas, and mixed oligoastrocytomas
  publication-title: J Clin Oncol
  doi: 10.1200/JCO.2000.18.3.636
– ident: 2018022808151318000_38.4.678.27
  doi: 10.3174/ajnr.A3384
– ident: 2018022808151318000_38.4.678.22
  doi: 10.1093/neuonc/nov307
– ident: 2018022808151318000_38.4.678.9
– volume: 61
  start-page: 6713
  year: 2001
  ident: 2018022808151318000_38.4.678.11
  article-title: Tumor location and growth pattern correlate with genetic signature in oligodendroglial neoplasms
  publication-title: Cancer Res
– ident: 2018022808151318000_38.4.678.21
  doi: 10.1172/JCI67229
– ident: 2018022808151318000_38.4.678.2
  doi: 10.1200/JCO.2013.49.3726
– ident: 2018022808151318000_38.4.678.20
  doi: 10.1126/scitranslmed.3002693
– ident: 2018022808151318000_38.4.678.3
  doi: 10.1200/JCO.2012.43.2229
– ident: 2018022808151318000_38.4.678.18
  doi: 10.1136/jnnp.2009.178806
– ident: 2018022808151318000_38.4.678.24
  doi: 10.3892/ol.2014.2013
– ident: 2018022808151318000_38.4.678.12
  doi: 10.1212/01.WNL.0000148642.26985.68
– ident: 2018022808151318000_38.4.678.28
  doi: 10.3174/ajnr.A3352
– ident: 2018022808151318000_38.4.678.23
  doi: 10.1038/srep16238
– ident: 2018022808151318000_38.4.678.29
  doi: 10.1007/s10014-016-0249-5
– ident: 2018022808151318000_38.4.678.25
  doi: 10.1007/s00330-015-4025-4
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Snippet In 2016, the World Health Organization revised the brain tumor classification, making mutation and 1p/19q codeletion the defining features of...
The authors wanted to determine whether imaging characteristics previously associated with oligodendroglial tumors were still applicable given the 2016 WHO...
BACKGROUND AND PURPOSEIn 2016, the World Health Organization revised the brain tumor classification, making IDH mutation and 1p/19q codeletion the defining...
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StartPage 678
SubjectTerms Adult
Adult Brain
Aged
Borders
Brain
Brain architecture
Brain cancer
Brain Neoplasms - diagnostic imaging
Brain Neoplasms - genetics
Brain Neoplasms - pathology
Brain tumors
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 19
Classification
Fellows' Journal Club
Female
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Title Genetically Defined Oligodendroglioma Is Characterized by Indistinct Tumor Borders at MRI
URI https://www.ncbi.nlm.nih.gov/pubmed/28126746
https://www.proquest.com/docview/1981058232
https://www.proquest.com/docview/1862764690
https://www.proquest.com/docview/1891881515
https://pubmed.ncbi.nlm.nih.gov/PMC7960254
Volume 38
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