Pediatric spinal high-grade glioma in the pediatric precision oncology registry INFORM: Identification of potential therapeutic targets.

IF 4.1 Q1 CLINICAL NEUROLOGY Neuro-oncology advances Pub Date : 2024-11-08 eCollection Date: 2025-01-01 DOI:10.1093/noajnl/vdae185
Elke Pfaff, Kathrin Schramm, Mirjam Blattner-Johnson, Barbara C Jones, Sebastian Stark, Gnana Prakash Balasubramanian, Christopher Previti, Robert J Autry, Petra Fiesel, Felix Sahm, David Reuss, Andreas von Deimling, Cornelis M van Tilburg, Kristian W Pajtler, Till Milde, Uta Dirksen, Christof M Kramm, André O von Bueren, Monica C Munthe-Kaas, Ingrid Øra, Stefan M Pfister, Olaf Witt, David T W Jones
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Abstract

Background: High-grade glioma (HGG) of the spinal cord constitutes rare tumors in the pediatric population. Knowledge of the molecular profile of this pediatric HGG (pedHGG) subgroup is limited and the clinical outcome is poor. Therefore, the aim of this study is to provide more profound investigations of molecular characteristics and clinical features of these tumors.

Methods: Between January 2015 and October 2023, 17 spinal tumors with HGG histology were analyzed by the Individualized Therapy For Relapsed Malignancies in Childhood (INFORM) precision oncology registry. Comprehensive molecular profiling (including next-generation sequencing approaches and DNA methylation analysis) was performed. Clinical data provided by the treating centers were evaluated regarding treatment approaches and outcomes.

Results: Subgroup classification based on DNA methylation analysis revealed molecular HGG subgroups in 12/17 cases, while 2/17 were classified as molecular low-grade glioma (LGG) and 3/17 were not unequivocally classifiable. Typical genetic alterations described in pedHGG usually presenting at other localizations were also present in the counterparts located in the spinal cohort. Alterations that might serve as a promising target for personalized therapy approaches were identified in a subset of tumors.

Conclusion: With this cohort of 12 molecularly confirmed spinal pedHGG cases, we provide a compilation of genomic as well as clinical features of this rare subgroup, contributing to a better understanding and eventually to future treatment approaches.

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儿童脊柱高级胶质瘤在儿科精确肿瘤学注册通知:潜在治疗靶点的识别。
背景:脊髓高级别胶质瘤(HGG)是儿科人群中罕见的肿瘤。对这种儿童HGG (pedHGG)亚组的分子谱的了解有限,临床结果很差。因此,本研究的目的是对这些肿瘤的分子特征和临床特征进行更深入的研究。方法:2015年1月至2023年10月,通过儿童复发恶性肿瘤个体化治疗(INFORM)精确肿瘤学登记处对17例HGG组织学的脊柱肿瘤进行分析。进行了全面的分子分析(包括下一代测序方法和DNA甲基化分析)。对治疗中心提供的临床数据进行治疗方法和结果评估。结果:基于DNA甲基化分析的亚组分类显示12/17例患者为分子HGG亚组,2/17例为分子低级别胶质瘤(LGG), 3/17例无法明确分类。在pedHGG中描述的通常出现在其他部位的典型遗传改变也出现在脊柱队列中的对应基因中。在肿瘤的一个子集中发现了可能作为个性化治疗方法的有希望的靶点的改变。结论:通过12例经分子证实的脊柱pedHGG病例,我们提供了这一罕见亚组的基因组和临床特征汇编,有助于更好地理解并最终为未来的治疗方法做出贡献。
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CiteScore
6.20
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审稿时长
12 weeks
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