Literature DB >> 26385879

Allelic loss of 9p21.3 is a prognostic factor in 1p/19q codeleted anaplastic gliomas.

Agustí Alentorn1, Caroline Dehais1, François Ducray1, Catherine Carpentier1, Karima Mokhtari1, Dominique Figarella-Branger1, Olivier Chinot1, Elisabeth Cohen-Moyal1, Carole Ramirez1, Hugues Loiseau1, Selma Elouahdani-Hamdi1, Patrick Beauchesne1, Olivier Langlois1, Christine Desenclos1, Jean-Sébastien Guillamo1, Phong Dam-Hieu1, François Ghiringhelli1, Philippe Colin1, Joel Godard1, Fabrice Parker1, Frédéric Dhermain1, Antoine F Carpentier1, Jean-Sebastien Frenel1, Philippe Menei1, Luc Bauchet1, Thierry Faillot1, Mélanie Fesneau1, Denys Fontaine1, Marie-Jeannette Motuo-Fotso1, Elodie Vauleon1, Claude Gaultier1, Caroline Le Guerinel1, Edouard-Marcel Gueye1, Georges Noel1, Nicolas Desse1, Xavier Durando1, Eduardo Barrascout1, Michel Wager1, Damien Ricard1, Ioana Carpiuc1, Jean-Yves Delattre1, Ahmed Idbaih2.   

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.
© 2015 American Academy of Neurology.

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Year:  2015        PMID: 26385879      PMCID: PMC4617162          DOI: 10.1212/WNL.0000000000002014

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


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