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

Agustì Alentorn, Caroline Dehais, Fraņois Ducray, Catherine Carpentier, Karima Mokhtari, Dominique Figarella-Branger, Olivier Chinot, Elisabeth Cohen-Moyal, Carole Ramirez, Hugues Loiseau, Selma Elouahdani-Hamdi, Patrick Beauchesne, Olivier Langlois, Christine Desenclos, Jean Sébastien Guillamo, Phong Dam-Hieu, Fraņois Ghiringhelli, Philippe Colin, Joel Godard, Fabrice ParkerFrédéric Dhermain, Antoine F. Carpentier, Jean Sebastien Frenel, Philippe Menei, Luc Bauchet, Thierry Faillot, Mélanie Fesneau, Denys Fontaine, Marie Jeannette Motuo-Fotso, Elodie Vauleon, Claude Gaultier, Caroline Le Guerinel, Edouard Marcel Gueye, Georges Noel, Nicolas Desse, Xavier Durando, Eduardo Barrascout, Michel Wager, Damien Ricard, Ioana Carpiuc, Jean Yves Delattre, Ahmed Idbaih

    Résultats de recherche: Contribution à un journalArticleRevue par des pairs

    29 Citations (Scopus)

    Résumé

    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 5 0.008 and p , 0.001, respectively) and multivariate analyses (p 5 0.009 and p 5 0.009, respectively). This finding was validated in the REMBRANDT dataset in univariate and multivariate analysis (p 5 0.01 and p 5 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.

    langue originaleAnglais
    Pages (de - à)1325-1331
    Nombre de pages7
    journalNeurology
    Volume85
    Numéro de publication15
    Les DOIs
    étatPublié - 13 oct. 2015

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