Details

Autor(en) / Beteiligte

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

Titel

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

Ist Teil von

• Neurology, 2015-10, Vol.85 (15), p.1325-1331

Ort / Verlag

United States

Erscheinungsjahr

2015

Quelle

MEDLINE

Beschreibungen/Notizen

• 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). 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. 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). Our study highlights a novel potential prognostic biomarker in 1p/19q codeleted AOT. Further prospective studies are warranted to investigate our finding.