Clinical Cooperation Unit Neuropathology (B300), German Cancer Research Center (DKFZ), German Cancer Consortium (DKTK), and National Center for Tumor Diseases (NCT), Im Neuenheimer Feld 280, 69120, Heidelberg, Germany.
Department of Neuropathology, Heidelberg University Hospital, Heidelberg, Germany.
Acta Neuropathol. 2023 Jun;145(6):829-842. doi: 10.1007/s00401-023-02575-z. Epub 2023 Apr 24.
Medulloblastoma (MB), one of the most common malignant pediatric brain tumor, is a heterogenous disease comprised of four distinct molecular groups (WNT, SHH, Group 3, Group 4). Each of these groups can be further subdivided into second-generation MB (SGS MB) molecular subgroups, each with distinct genetic and clinical characteristics. For instance, non-WNT/non-SHH MB (Group 3/4) can be subdivided molecularly into eight distinct and clinically relevant tumor subgroups. A further molecular stratification/summarization of these SGS MB would allow for the assignment of patients to risk-associated treatment protocols. Here, we performed DNA- and RNA-based analysis of 574 non-WNT/non-SHH MB and analyzed the clinical significance of various molecular patterns within the entire cohort and the eight SGS MB, with the aim to develop an optimal risk stratification of these tumors. Multigene analysis disclosed several survival-associated genes highly specific for each molecular subgroup within this non-WNT/non-SHH MB cohort with minimal inter-subgroup overlap. These subgroup-specific and prognostically relevant genes were associated with pathways that could underlie SGS MB clinical-molecular diversity and tumor-driving mechanisms. By combining survival-associated genes within each SGS MB, distinct metagene sets being appropriate for their optimal risk stratification were identified. Defined subgroup-specific metagene sets were independent variables in the multivariate models generated for each SGS MB and their prognostic value was confirmed in a completely non-overlapping validation cohort of non-WNT/non-SHH MB (n = 377). In summary, the current results indicate that the integration of transcriptome data in risk stratification models may improve outcome prediction for each non-WNT/non-SHH SGS MB. Identified subgroup-specific gene expression signatures could be relevant for clinical implementation and survival-associated metagene sets could be adopted for further SGS MB risk stratification. Future studies should aim at validating the prognostic role of these transcriptome-based SGS MB subtypes in prospective clinical trials.
髓母细胞瘤(MB)是最常见的儿童恶性脑肿瘤之一,是一种异质性疾病,由四个不同的分子群(WNT、SHH、Group 3、Group 4)组成。这些群体中的每一个都可以进一步细分为第二代髓母细胞瘤(SGS MB)分子亚群,每个亚群都具有独特的遗传和临床特征。例如,非 WNT/非 SHH MB(Group 3/4)可以在分子水平上进一步细分为八个不同的、具有临床相关性的肿瘤亚群。对这些 SGS MB 进行进一步的分子分层/总结,可以将患者分配到与风险相关的治疗方案中。在这里,我们对 574 例非 WNT/非 SHH MB 进行了基于 DNA 和 RNA 的分析,并分析了整个队列和八个 SGS MB 中各种分子模式的临床意义,旨在对这些肿瘤进行最佳的风险分层。多基因分析揭示了几个与每个分子亚群高度相关的生存相关基因,这些基因在非 WNT/非 SHH MB 亚群中具有最小的亚群重叠。这些亚群特异性和预后相关的基因与可能是 SGS MB 临床-分子多样性和肿瘤驱动机制基础的途径有关。通过组合每个 SGS MB 中的生存相关基因,确定了适合其最佳风险分层的不同元基因集。在为每个 SGS MB 生成的多变量模型中,定义的亚群特异性元基因集是独立变量,在非 WNT/非 SHH MB 的完全非重叠验证队列(n=377)中验证了它们的预后价值。总之,目前的结果表明,将转录组数据整合到风险分层模型中可能会提高每个非 WNT/非 SHH SGS MB 的预后预测。鉴定的亚群特异性基因表达特征可能与临床实施相关,而与生存相关的元基因集可用于进一步的 SGS MB 风险分层。未来的研究应旨在前瞻性临床试验中验证这些基于转录组的 SGS MB 亚型的预后作用。