Allelic loss of 9p21.3 is a prognostic factor in 1p/19q codeleted anaplastic gliomas
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Abstract
Objectives: We aimed to study the potential clinical relevance of 9p allelic loss, with or without copy number variation, in 1p/19q codeleted anaplastic oligodendroglial tumors (AOTs).
Methods: This study enrolled 216 patients with 1p/19q codeleted AOT. The prognostic value of 9p allelic loss was investigated using a French nation-wide prospective registry, POLA (prise en charge des tumeurs oligodendrogliales anaplasiques) and high-density single nucleotide polymorphism arrays. We validated our results using the Repository of Molecular Brain Neoplasia Data (REMBRANDT) dataset.
Results: The minimal common region of allelic loss in chromosome arm 9p was 9p21.3. Allelic loss of 9p21.3, detected in 41.7% of tumors, was associated with shorter progression-free and overall survival rates in univariate (p = 0.008 and p < 0.001, respectively) and multivariate analyses (p = 0.009 and p = 0.009, respectively). This finding was validated in the REMBRANDT dataset in univariate and multivariate analysis (p = 0.01 and p = 0.01, respectively).
Conclusion: Our study highlights a novel potential prognostic biomarker in 1p/19q codeleted AOT. Further prospective studies are warranted to investigate our finding.
GLOSSARY
- AOT=
- anaplastic oligodendroglial tumor;
- CN-LOH=
- copy neutral loss of heterozygosity;
- HR=
- hazard ratio;
- MCR=
- minimal common region;
- OS=
- overall survival;
- PCV=
- procarbazine-CCNU-vincristine;
- PFS=
- progression-free survival;
- POLA=
- prise en charge des tumeurs oligodendrogliales anaplasiques;
- REMBRANDT=
- Repository of Molecular Brain Neoplasia Data;
- RT=
- radiotherapy;
- WHO=
- World Health Organization
Footnotes
POLA Network coinvestigators are listed on the Neurology® Web site at Neurology.org.
Go to Neurology.org for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.
Supplemental data at Neurology.org
- Received November 8, 2014.
- Accepted in final form June 17, 2015.
- © 2015 American Academy of Neurology
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