Institute of Neuropathology, University of Bonn Medical Center, Bonn, Germany.
Acta Neuropathol. 2014 Jul;128(1):137-49. doi: 10.1007/s00401-014-1276-0. Epub 2014 May 4.
This study aimed to prospectively evaluate clinical, histopathological and molecular variables for outcome prediction in medulloblastoma patients. Patients from the HIT2000 cooperative clinical trial were prospectively enrolled based on the availability of sufficient tumor material and complete clinical information. This revealed a cohort of 184 patients (median age 7.6 years), which was randomly split at a 2:1 ratio into a training (n = 127), and a test (n = 57) dataset in order to build and test a risk score for this population. Independent validation was performed in a non-overlapping cohort (n = 83). All samples were subjected to thorough histopathological investigation, CTNNB1 mutation analysis, quantitative PCR, MLPA and FISH analyses for cytogenetic variables, and methylome analysis. By univariable analysis, clinical factors (M-stage), histopathological variables (large cell component, endothelial proliferation, synaptophysin pattern), and molecular features (chromosome 6q status, MYC amplification, subgrouping) were found to be prognostic. Molecular consensus subgrouping (WNT, SHH, Group 3, Group 4) was validated as an independent feature to stratify patients into different risk groups. When comparing methods for the identification of WNT-driven medulloblastoma, this study identified CTNNB1 sequencing and methylation profiling to most reliably identify these patients. After removing patients with particularly favorable (CTNNB1 mutation, extensive nodularity) or unfavorable (MYC amplification) markers, a risk score for the remaining "intermediate molecular risk" population dependent on age, M-stage, pattern of synaptophysin expression, and MYCN copy-number status was identified, with speckled synaptophysin expression indicating worse outcome. Test and independent validation of the score confirmed significant discrimination of patients by risk profile. Methylation subgrouping and CTNNB1 mutation status represent robust tools for the risk stratification of medulloblastoma. A simple clinico-pathological risk score was identified, which was confirmed in a test set and by independent clinical validation.
本研究旨在前瞻性评估髓母细胞瘤患者的临床、组织病理学和分子变量,以预测其预后。根据肿瘤组织标本的可用性和完整的临床资料,从 HIT2000 合作临床试验中前瞻性纳入患者。这揭示了一个包含 184 例患者(中位年龄为 7.6 岁)的队列,该队列按照 2:1 的比例随机分为训练(n=127)和测试(n=57)数据集,以建立和测试该人群的风险评分。在非重叠队列(n=83)中进行了独立验证。所有样本均进行了详细的组织病理学研究、CTNNB1 突变分析、定量 PCR、MLPA 和染色体核型分析,以及甲基组分析。通过单变量分析,临床因素(M 期)、组织病理学变量(大细胞成分、内皮增殖、突触素模式)和分子特征(染色体 6q 状态、MYC 扩增、亚组分类)被发现具有预后意义。分子共识亚组分类(WNT、SHH、Group 3、Group 4)被验证为独立特征,可将患者分为不同的风险组。在比较鉴定 WNT 驱动型髓母细胞瘤的方法时,本研究发现 CTNNB1 测序和甲基化谱分析最可靠地识别这些患者。在排除具有特别有利(CTNNB1 突变、广泛结节性)或不利(MYC 扩增)标志物的患者后,根据年龄、M 期、突触素表达模式和 MYCN 拷贝数状态,确定了一个依赖于剩余“中间分子风险”人群的风险评分,点状突触素表达预示着更差的预后。对该评分的测试和独立验证确认了风险特征对患者的显著区分。甲基化亚组分类和 CTNNB1 突变状态是髓母细胞瘤风险分层的有力工具。已经确定了一个简单的临床病理风险评分,并在测试集和独立的临床验证中得到了验证。