Division of Neuro-Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Harvard Medical School, Boston, Massachusetts.
JAMA Oncol. 2022 Oct 1;8(10):1493-1501. doi: 10.1001/jamaoncol.2022.2844.
Previous histologic classifications of brain tumors have been limited by discrepancies in diagnoses reported by neuropathologists and variability in outcomes and response to therapies. Such diagnostic discrepancies have impaired clinicians' ability to select the most appropriate therapies for patients and have allowed heterogeneous populations of patients to be enrolled in clinical trials, hindering the development of more effective therapies. In adult-type diffuse gliomas, histologic classification has a particularly important effect on clinical care.
In 2021, the World Health Organization published the fifth edition of the Classification of Tumors of the Central Nervous System. This classification incorporates advances in understanding the molecular pathogenesis of brain tumors with histopathology in order to group tumors into more biologically and molecularly defined entities. As such, tumor classification is significantly improved through better characterized natural histories. These changes have particularly important implications for gliomas. For the first time, adult- and pediatric-type gliomas are classified separately on the basis of differences in molecular pathogenesis and prognosis. Furthermore, the previous broad category of adult-type diffuse gliomas has been consolidated into 3 types: astrocytoma, isocitrate dehydrogenase (IDH) mutant; oligodendroglioma, IDH mutant and 1p/19q codeleted; and glioblastoma, IDH wild type. These major changes are driven by IDH mutation status and include the restriction of the diagnosis of glioblastoma to tumors that are IDH wild type; the reclassification of tumors previously diagnosed as IDH-mutated glioblastomas as astrocytomas IDH mutated, grade 4; and the requirement for the presence of IDH mutations to classify tumors as astrocytomas or oligodendrogliomas.
The 2021 World Health Organization central nervous system tumor classification is a major advance toward improving the diagnosis of brain tumors. It will provide clinicians with more accurate guidance on prognosis and optimal therapy for patients and ensure that more homogenous patient populations are enrolled in clinical trials, potentially facilitating the development of more effective therapies.
以前的脑肿瘤组织学分类受到神经病理学家报告的诊断差异以及治疗结果和反应的可变性的限制。这种诊断差异削弱了临床医生为患者选择最合适治疗方法的能力,并允许不同人群的患者入组临床试验,从而阻碍了更有效的治疗方法的发展。在成人型弥漫性胶质瘤中,组织学分类对临床护理有特别重要的影响。
2021 年,世界卫生组织发布了第五版《中枢神经系统肿瘤分类》。该分类将脑肿瘤的分子发病机制与组织病理学相结合,以便将肿瘤分为更具生物学和分子定义的实体。因此,通过更好地描述自然病史,肿瘤分类得到了显著改善。这些变化对胶质瘤尤其重要。首次根据分子发病机制和预后的差异,将成人型和儿童型胶质瘤分开分类。此外,以前的成人型弥漫性胶质瘤的广泛类别已被合并为 3 种类型:星形细胞瘤,异柠檬酸脱氢酶(IDH)突变型;少突胶质细胞瘤,IDH 突变型和 1p/19q 缺失型;胶质母细胞瘤,IDH 野生型。这些重大变化是由 IDH 突变状态驱动的,包括将 IDH 野生型肿瘤诊断为胶质母细胞瘤;将以前诊断为 IDH 突变型胶质母细胞瘤的肿瘤重新分类为 IDH 突变型星形细胞瘤,4 级;以及要求 IDH 突变存在才能将肿瘤分类为星形细胞瘤或少突胶质细胞瘤。
2021 年世界卫生组织中枢神经系统肿瘤分类是朝着改善脑肿瘤诊断迈出的重大一步。它将为临床医生提供更准确的预后和最佳治疗建议,确保更同质的患者人群入组临床试验,从而有可能促进更有效的治疗方法的发展。