Department of Pathology and Laboratory Medicine, Nationwide Children's Hospital, Columbus, OH, USA; Department of Pathology, The Ohio State University College of Medicine, Columbus, OH, USA.
Chin Clin Oncol. 2023 Feb;12(1):7. doi: 10.21037/cco-22-120.
In 2021, the World Health Organization (WHO) Classification of Tumors of the Central Nervous System (CNS) underwent significant restructuring to incorporate additional molecular diagnostics, several newly recognized tumor types, and new grading schemes for existing tumor types. The 2021 CNS WHO classification further elaborates and integrates histopathologic and molecular diagnostic criteria to improve diagnostic classification. Furthermore, it is the hope that identification of molecular alterations in pediatric and adult tumors facilitates improved prognostic information and development of novel targeted therapies for adults and children with CNS tumors. In one of the largest changes in the new WHO classification, diffuse gliomas are divided into pediatric-type and adult-type gliomas to highlight our expanding knowledge of their different molecular drivers and prognostic associations. Several new pediatric-type diffuse low-grade gliomas are defined including (I) diffuse astrocytoma, MYB- or MYBL1-altered, (II) polymorphous low-grade neuroepithelial tumor of the young (PLNTY), and (III) diffuse low-grade glioma, MAPK-pathway altered. In addition, several new pediatric-type diffuse high-grade gliomas are recognized including (I) diffuse hemispheric glioma, H3 G34R-mutant (II) diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype, and (III) infant-type hemispheric glioma. These new tumor types have associated clinical, genetic and epigenetic features that are distinct from adult-type diffuse gliomas. This review provides an overview of updates in the 2021 CNS WHO classification specific to diffuse gliomas, with a particular focus on the histopathology and molecular findings of the newly described pediatric-type low-grade and high-grade gliomas.
2021 年,世界卫生组织(WHO)中枢神经系统(CNS)肿瘤分类进行了重大调整,纳入了更多的分子诊断、几种新识别的肿瘤类型,以及对现有肿瘤类型的新分级方案。2021 年 CNS WHO 分类进一步阐述和整合了组织病理学和分子诊断标准,以提高诊断分类。此外,希望在儿科和成人肿瘤中识别分子改变,为 CNS 肿瘤的成人和儿童提供更好的预后信息,并开发新的靶向治疗方法。在新 WHO 分类中的最大变化之一是,弥漫性胶质瘤分为儿科型和成人型胶质瘤,以突出我们对其不同分子驱动因素和预后相关性的认识不断扩大。定义了几种新的儿科型弥漫性低级别胶质瘤,包括(I)弥漫性星形细胞瘤,MYB 或 MYBL1 改变,(II)年轻多形性低度神经上皮肿瘤(PLNTY),和(III)弥漫性低级别胶质瘤,MAPK 通路改变。此外,还认识到几种新的儿科型弥漫性高级别胶质瘤,包括(I)弥漫性大脑半球胶质瘤,H3 G34R 突变(II)弥漫性儿科型高级别胶质瘤,H3 野生型和 IDH 野生型,和(III)婴儿型大脑半球胶质瘤。这些新的肿瘤类型具有独特的临床、遗传和表观遗传特征,与成人型弥漫性胶质瘤不同。这篇综述提供了 2021 年 CNS WHO 分类中关于弥漫性胶质瘤的更新概述,特别关注新描述的儿科型低级别和高级别胶质瘤的组织病理学和分子发现。