The Neurogenome study: Comprehensive molecular profiling to optimize treatment for Danish glioblastoma patients

IF 3.7 Q1 CLINICAL NEUROLOGY
Dorte Schou Nørøxe, Simone Maarup, Vincent Fougner, Aida Muhic, Søren Møller, Thomas Urup, Maya Jeje Schuang Lü, Joachim Weischenfeldt, Adam Espe Hansen, Hans Skovgaard Poulsen, Ulrik Lassen, Benedikte Hasselbalch
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引用次数: 0

Abstract

Abstract Background Glioblastoma is an aggressive brain cancer with no possibility for cure. Treatment and survival have only improved slightly since 2005 when the current regime was implemented. The limited improvements in the treatment of glioblastoma, may reflect our poor understanding of the disease. We hypothesize that systematically collected translational data will improve knowledge and hereby treatment. Methods We have been performing whole exome sequencing in glioblastoma tumor tissue since 2016 and whole genome sequencing since 2020 with the aim of offering experimental treatment. Results We have sequenced 400+ GBM patients and from these 100+ are paired tumor samples from relapse surgery. To develop genomic profiling and to increase the information of each patient´s contribution, we have initiated the Neurogenome study as of June 2022. The Neurogenome protocol is a national, comprehensive, translational, omic-protocol. It is a continuation of two previous protocols from 2016 and forth in our department, but with more sub studies added, focusing on the translational and clinical utility. We collect and analyze data from an out-patient clinic in a systematically approach to a number of subprojects ranging from basic science to applied clinical science, including clinical trials. Conclusion The protocol will act as backbone for future projects in the national research center, Danish Comprehensive Cancer Center - Brain Tumor Center with the overall aim to select eligible patients for experimental treatment based upon genomic alterations. The article will present the Neurogenome setup and a presentation of selected projects that are based upon inclusion.
神经基因组研究:综合分子分析优化丹麦胶质母细胞瘤患者的治疗
背景:胶质母细胞瘤是一种侵袭性脑癌,没有治愈的可能性。自2005年实施现行制度以来,治疗和生存率仅略有改善。胶质母细胞瘤的治疗进展有限,这可能反映了我们对这种疾病的了解不足。我们假设系统收集的翻译数据将改善知识和治疗。方法我们从2016年开始在胶质母细胞瘤肿瘤组织中进行全外显子组测序,从2020年开始进行全基因组测序,目的是提供实验性治疗。结果我们对400多例GBM患者进行了测序,其中100多例为复发手术的配对肿瘤样本。为了开发基因组分析并增加每个患者贡献的信息,我们已于2022年6月启动了神经基因组研究。神经基因组协议是一项全国性的、综合性的、可翻译的基因组协议。这是我们科室2016年及以后的两项协议的延续,但增加了更多的子研究,重点是转化和临床应用。我们以系统的方法收集和分析门诊诊所的数据,以一些子项目,从基础科学到应用临床科学,包括临床试验。该方案将成为国家研究中心丹麦综合癌症中心-脑肿瘤中心未来项目的支柱,其总体目标是选择符合条件的患者进行基于基因组改变的实验性治疗。这篇文章将介绍神经基因组的设置和基于纳入的选定项目的介绍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.20
自引率
0.00%
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0
审稿时长
12 weeks
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