Pfaff Elke, Schramm Kathrin, Blattner-Johnson Mirjam, Jones Barbara C, Stark Sebastian, Balasubramanian Gnana Prakash, Previti Christopher, Autry Robert J, Fiesel Petra, Sahm Felix, Reuss David, von Deimling Andreas, van Tilburg Cornelis M, Pajtler Kristian W, Milde Till, Dirksen Uta, Kramm Christof M, von Bueren André O, Munthe-Kaas Monica C, Øra Ingrid, Pfister Stefan M, Witt Olaf, Jones David T W
Department of Pediatric Oncology, Hematology, Immunology and Pulmonology, Heidelberg University Hospital, Heidelberg, Germany.
German Cancer Research Center (DKFZ), Heidelberg, Germany.
Neurooncol Adv. 2024 Nov 8;7(1):vdae185. doi: 10.1093/noajnl/vdae185. eCollection 2025 Jan-Dec.
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.
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.
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.
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.
脊髓高级别胶质瘤(HGG)在儿科人群中属于罕见肿瘤。对该儿科HGG(pedHGG)亚组分子特征的了解有限,且临床预后较差。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。
在2015年1月至2023年10月期间,通过儿童复发性恶性肿瘤个体化治疗(INFORM)精准肿瘤登记系统对17例具有HGG组织学特征的脊髓肿瘤进行了分析。进行了全面的分子谱分析(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了治疗方法和预后评估。
基于DNA甲基化分析的亚组分类显示,17例中有12例为分子HGG亚组,2例为分子低级别胶质瘤(LGG),3例无法明确分类。pedHGG中通常在其他部位出现的典型基因改变在脊髓队列中的对应病例中也存在。在一部分肿瘤中发现了可能作为个性化治疗方法有前景靶点的改变。
通过这组12例分子确诊的脊髓pedHGG病例,我们提供了这个罕见亚组的基因组以及临床特征汇编,有助于更好地理解并最终推动未来的治疗方法。