ATRX公司
胶质瘤
PTEN公司
替莫唑胺
癌症研究
脑瘤
医学
IDH1
癌症
肿瘤科
突变
胶质母细胞瘤
病理
内科学
生物
基因
遗传学
细胞凋亡
PI3K/AKT/mTOR通路
作者
Christian Mawrin,Michael Luchtmann,Elmar Kirches
出处
期刊:Neuro-oncology
[Oxford University Press]
日期:2023-11-01
卷期号:25 (Supplement_5): v176-v177
标识
DOI:10.1093/neuonc/noad179.0668
摘要
Abstract INTRODUCTION This study aims to investigate the molecular characterization of glioma tissue after treatment with Tumor Treating Fields (TTFields). TTFields therapy utilizes low-intensity alternating electric fields to disrupt cancer cell division and is approved for treatment of glioblastoma as well as mesothelioma. Understanding the histological, cellular, and epigenetic changes induced by TTFields treatment can help identify biomarkers for TTFields response and elucidate potential resistance mechanisms. MATERIAL AND METHODS Tumor tissue samples (FFPE) were collected from newly diagnosed glioblastoma patients treated with TTFields, including both the primary tumor and matching recurrent tumor samples. Molecular analyses using a glioma-targeted next-generation sequencing (NGS) panel sequencing were performed to assess genetic alterations in both primary and recurrent tumors. RESULTS Genomic analysis of paired samples from 5 patients (4 glioblastoma, one astrocytoma, IDH-mutated WHO grade 4) revealed an identical molecular pattern (TERT mutation) in 2 patients, one patient with a gain of an ATRX mutation in the recurrent tumor, one patient with gain of two EGFR mutations, and the IDH1-mutated astrocytoma showing a loss of a TP53 mutation in the recurrent tumor. CONCLUSION This pilot study provides valuable insights into the molecular characterization of glioma tissue after TTFields treatment. It appears that the spectrum of mutations may vary in a substantial number of TTF-treated tumors. Further validation and larger-scale studies are needed to confirm and expand upon these preliminary results.
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