Polysomy is associated with poor outcome in 1p/19q codeleted oligodendroglial tumors.


Journal

Neuro-oncology
ISSN: 1523-5866
Titre abrégé: Neuro Oncol
Pays: England
ID NLM: 100887420

Informations de publication

Date de publication:
06 09 2019
Historique:
pubmed: 30 5 2019
medline: 11 11 2020
entrez: 30 5 2019
Statut: ppublish

Résumé

Chromosomal instability is associated with earlier progression in isocitrate dehydrogenase (IDH)-mutated astrocytomas. Here we evaluated the prognostic significance of polysomy in gliomas tested for 1p/19q status. We analyzed 412 histologic oligodendroglial tumors with use of 1p/19q testing at 8 institutions from 1996 to 2013; fluorescence in situ hybridization (FISH) for 1p/19q was performed. Polysomy was defined as more than two 1q and 19p signals in cells. Tumors were divided into groups on the basis of their 1p/19q status and polysomy and were compared for progression-free survival (PFS) and overall survival (OS). In our cohort, 333 tumors (81%) had 1p/19q loss; of these, 195 (59%) had concurrent polysomy and 138 (41%) lacked polysomy, 79 (19%) had 1p/19q maintenance; of these, 30 (38%) had concurrent polysomy and 49 (62%) lacked polysomy. In agreement with prior studies, the group with 1p/19q loss had significantly better PFS and OS than did the group with 1p/19q maintenance (P < 0.0001 each). Patients with 1p/19q loss and polysomy showed significantly shorter PFS survival than patients with 1p/19q codeletion only (P < 0.0001), but longer PFS and OS than patients with 1p/19q maintenance (P < 0.01 and P < 0.0001). There was no difference in survival between tumors with >30% polysomic cells and those with <30% polysomic cells. Polysomy had no prognostic significance on PFS or OS in patients with 1p/19q maintenance. The presence of polysomy in oligodendroglial tumors with codeletion of 1p/19q predicts early recurrence and short survival in patients with 1p/19q codeleted tumors.

Sections du résumé

BACKGROUND
Chromosomal instability is associated with earlier progression in isocitrate dehydrogenase (IDH)-mutated astrocytomas. Here we evaluated the prognostic significance of polysomy in gliomas tested for 1p/19q status.
METHODS
We analyzed 412 histologic oligodendroglial tumors with use of 1p/19q testing at 8 institutions from 1996 to 2013; fluorescence in situ hybridization (FISH) for 1p/19q was performed. Polysomy was defined as more than two 1q and 19p signals in cells. Tumors were divided into groups on the basis of their 1p/19q status and polysomy and were compared for progression-free survival (PFS) and overall survival (OS).
RESULTS
In our cohort, 333 tumors (81%) had 1p/19q loss; of these, 195 (59%) had concurrent polysomy and 138 (41%) lacked polysomy, 79 (19%) had 1p/19q maintenance; of these, 30 (38%) had concurrent polysomy and 49 (62%) lacked polysomy. In agreement with prior studies, the group with 1p/19q loss had significantly better PFS and OS than did the group with 1p/19q maintenance (P < 0.0001 each). Patients with 1p/19q loss and polysomy showed significantly shorter PFS survival than patients with 1p/19q codeletion only (P < 0.0001), but longer PFS and OS than patients with 1p/19q maintenance (P < 0.01 and P < 0.0001). There was no difference in survival between tumors with >30% polysomic cells and those with <30% polysomic cells. Polysomy had no prognostic significance on PFS or OS in patients with 1p/19q maintenance.
CONCLUSIONS
The presence of polysomy in oligodendroglial tumors with codeletion of 1p/19q predicts early recurrence and short survival in patients with 1p/19q codeleted tumors.

Identifiants

pubmed: 31140557
pii: 5505367
doi: 10.1093/neuonc/noz098
pmc: PMC7571489
doi:

Substances chimiques

IDH2 protein, human EC 1.1.1.41
Isocitrate Dehydrogenase EC 1.1.1.41
IDH1 protein, human EC 1.1.1.42.

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1164-1174

Subventions

Organisme : NINDS NIH HHS
ID : R01 NS102669
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS102665
Pays : United States
Organisme : NINDS NIH HHS
ID : R03 NS087349
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA221747
Pays : United States

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

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Auteurs

Hui Chen (H)

Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, New York.

Cheddhi Thomas (C)

Department of Pathology, NYU Langone Health, New York, New York.

Felipe Andres Munoz (FA)

Department of Biostatistics and Epidemiology, Rutgers University, School of Public Health, Piscataway Township, New Jersey.

Sanda Alexandrescu (S)

Department of Pathology, University of California San Francisco, San Francisco, California.

Craig M Horbinski (CM)

Department of Pathology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.

Adriana Olar (A)

Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Declan McGuone (D)

Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Sandra Camelo-Piragua (S)

Department of Pathology, University of Michigan School of Medicine, Ann Arbor, Michigan.

Lu Wang (L)

Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, New York.

Elena Pentsova (E)

Department of Neurology, Memorial Sloan-Kettering Cancer Center, New York, New York.

Joanna Phillips (J)

Department of Neurological Surgery, University of California San Francisco, San Francisco, California.

Kenneth Aldape (K)

Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Wen Chen (W)

Department of Neurology, Memorial Sloan-Kettering Cancer Center, New York, New York.

A John Iafrate (AJ)

Pathology Service, Massachusetts General Hospital, Boston, Massachusetts.

Andrew S Chi (AS)

Neuro-Oncology Program, Perlmutter Cancer Center, NYU Langone Health, New York, New York.

David Zagzag (D)

Department of Neurosurgery, Perlmutter Cancer Center, NYU Langone Health, New York, New York.

John G Golfinos (JG)

Department of Neurosurgery, Perlmutter Cancer Center, NYU Langone Health, New York, New York.

Dimitris G Placantonakis (DG)

Department of Neurosurgery, Perlmutter Cancer Center, NYU Langone Health, New York, New York.
Kimmel Center for Stem Cell Biology, Neuroscience Institute, NYU Langone Health, New York, New York.

Marc Rosenblum (M)

Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, New York.

Pamela Ohman-Strickland (P)

Department of Biostatistics and Epidemiology, Rutgers University, School of Public Health, Piscataway Township, New Jersey.

Meera Hameed (M)

Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, New York.

Matija Snuderl (M)

Department of Pathology, NYU Langone Health, New York, New York.

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Classifications MeSH