Gupta Kirti, Salunke Pravin
Neuropathology fellowship (St Jude, Memphis), Department of Histopathology, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Department of Neurosurgery, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Mol Neurobiol. 2017 Jan;54(1):15-21. doi: 10.1007/s12035-015-9646-8. Epub 2015 Dec 28.
Remarkable progress has been made in the last decade in understanding the biology and oncogenesis of this relatively rare childhood brain tumor-the ependymoma. Surgery and irradiation are the mainstays of therapeutic options; chemotherapy is yet to predictably affect outcome, and its role is currently being explored in several clinical trials. While WHO scores this tumor into three grades, grading of ependymoma into grade II and grade III is controversial because of its elusive histological criteria where no cut-offs have been defined for mitoses or percentage of tumor depicting increased cellularity. Grading remains unreliable in predicting outcome in several instances. There is a compelling need to integrate the molecular biomarkers highlighted in several studies over the past decade into patient risk stratification to help in better predicting the clinical outcome and to design effective tailored therapy. Genomic and transcriptomic studies lately have defined distinct molecular subgroups within ependymoma arising at three anatomic compartments-supratentorial, posterior fossa, and spinal cord. Review of pertinent literature on several seminal studies that have established a paradigm shift in understanding the oncogenesis of ependymoma has been carried out. The outcome, impact, and clinical relevance of these studies are also discussed. The review provides an update on progress and recent advances in understanding the biology and oncogenesis of ependymoma. The establishment of robust subgroups which are demographically, clinically, and molecularly distinct will provide new avenues for further refinement of therapeutic strategies.
在过去十年中,对于这种相对罕见的儿童脑肿瘤——室管膜瘤的生物学特性和肿瘤发生机制的理解取得了显著进展。手术和放疗是主要的治疗选择;化疗对预后的影响尚未能确切预测,其作用目前正在多项临床试验中进行探索。虽然世界卫生组织将这种肿瘤分为三个级别,但室管膜瘤的二级和三级分级存在争议,因为其组织学标准难以捉摸,对于有丝分裂或显示细胞增多的肿瘤百分比没有明确的界定。在多种情况下,分级在预测预后方面仍然不可靠。迫切需要将过去十年多项研究中突出的分子生物标志物纳入患者风险分层,以更好地预测临床结果并设计有效的个性化治疗方案。最近的基因组和转录组研究已经在室管膜瘤中确定了不同的分子亚组,这些亚组起源于三个解剖部位——幕上、后颅窝和脊髓。本文对一些开创性研究的相关文献进行了综述,这些研究在理解室管膜瘤的肿瘤发生机制方面实现了范式转变。还讨论了这些研究的结果、影响和临床相关性。这篇综述提供了关于室管膜瘤生物学特性和肿瘤发生机制理解方面的进展和最新研究成果。建立在人口统计学、临床和分子层面都不同的强大亚组将为进一步优化治疗策略提供新途径。