Rapid fully-automated assay for routine molecular diagnosis of mutations for personalized therapy of low grade gliomas.
Fiche publication
Date publication
octobre 2019
Journal
Pediatric hematology and oncology
Auteurs
Membres identifiés du Cancéropôle Est :
Pr CHASTAGNER Pascal, Dr LEROUX Agnès, Pr MERLIN Jean-Louis, Pr GAUCHOTTE Guillaume, Dr GILSON Pauline
Tous les auteurs :
Merlin MS, Gilson P, Rouyer M, Chastagner P, Doz F, Varlet P, Leroux A, Gauchotte G, Merlin JL
Lien Pubmed
Résumé
mutation analysis is important to personalize the management with low-grade gliomas (LGG) in children and adults, with therapeutic and prognostic impacts. In recurrent tumors, targeted therapies such as BRAF inhibitors had been reported to induce disease stabilization and significant radiographic responses. This highlights the potential interest of mutation to stratify patients for targeted therapy. Standard operating procedures (SOP) for V600E mutation detection can be time-consuming and consequently delay treatment choice in patients with acute deterioration. Here, we evaluated Idylla fully automated PCR (FA-PCR) assay for the rapid determination of mutational status in children and adult LGG. Formalin-fixed and paraffin-embedded (FFPE) samples from three histological LGG subtypes (ganglioglioma, pleomorphic xantoastrocytoma, and dysembryoplastic neuroepithelial tumor) with previous SOP-characterized mutational status were re-analyzed using the FA-PCR. Overall concordance with the mutational status determined using SOP, as well as sensitivity and specificity of FA-PCR technique were assessed. All 14 samples gave interpretable results with FA-PCR. Overall concordance of mutational status between FA-PCR and SOP was 100%. Sensitivity and specificity were 100%. This study confirms the reliability of FA-PCR for mutations analysis in children and adult LGG. Considering the short time to results enabled by FA-PCR, providing results in less than 90 minutes, this technique represents an interesting option for the molecular diagnosis of LGG and personalization of treatment.
Mots clés
Automated real-time PCR, BRAF, low grade glioma, molecular diagnosis
Référence
Pediatr Hematol Oncol. 2019 Oct 23;:1-12