10006-PEDT-1 基因组医学时代的儿科低级别胶质瘤手术

Akira Gomi, Hirofumi Oguma, Kensuke Kawai
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摘要

在新的WHO 2021年脑肿瘤分类中,儿科型胶质瘤与成人型肿瘤分开分类。此外,随着癌症基因组学的进步,治疗选择也在扩大。这里我们考虑手术治疗小儿低级别胶质瘤。方法回顾性分析2002年至2023年3月在我院接受手术治疗的41例18岁以下低级别胶质瘤或胶质神经元肿瘤患者。我们讨论了基于分子分类的手术策略。结果胶质瘤34例,胶质神经元瘤7例。根据新的WHO分类,它们对应于1)成人型弥漫性胶质瘤,2)儿科型弥漫性低级别胶质瘤,3)限定星形细胞瘤,或4)胶质神经元和神经元肿瘤。根据世卫组织的新分类,还考虑了没有分子诊断的病例。累及大脑半球、脑干、脊髓的分子诊断星形细胞瘤中,1)无病例,2)3)为主要病例。在手术选择中需要注意的是,与成人类型相比,这些病例通常具有更有利的预后,并且有助于诊断导致分子靶向药物选择的MAPK通路异常。3)包括毛细胞星形细胞瘤、室管膜下巨细胞星形细胞瘤和多形性黄色星形细胞瘤。其中,在视神经通路和下丘脑的毛细胞星形细胞瘤的治疗中,活检对于分子诊断和选择合适的治疗剂是必要的。相反,对于单侧视神经胶质瘤,可以考虑除切除外的其他选择。4)主要与癫痫相关肿瘤有关。在这些病例中,手术切除有望控制癫痫。然而,已经确定了各种遗传异常,这在诊断和治疗中可能是有用的。结论根据世界卫生组织的新分类,有必要对儿童脑肿瘤的治疗策略进行重新评估。
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10006-PEDT-1 PEDIATRIC LOWER GRADE GLIOMA SURGERY IN THE ERA OF GENOMIC MEDICINE
Abstract INTRODUCTION In the new WHO Brain Tumor Classification of 2021, pediatric-type gliomas are classified separately from adult-type tumors. Additionally, with the advancement of cancer genomics, treatment options have expanded. Here we consider surgery for pediatric low-grade gliomas. METHODS We retrospectively analyzed 41 cases of low-grade gliomas or glioneuronal tumors in patients under 18 years of age who underwent surgery at our institute from 2002 to March 2023. We discussed surgical strategies based on molecular classification. RESULTS Among the cases, there were 34 gliomas and 7 glioneuronal tumors. According to the new WHO classification, they corresponded to 1) Adult-type diffuse gliomas, 2) Pediatric-type diffuse low-grade gliomas, 3) Circumscribed astrocytic tumors, or 4) Glioneuronal and neuronal tumors. Cases without molecular diagnosis were also considered in light of the new WHO classification. DISCUSSION Among molecularly diagnosed astrocytomas involving the cerebral hemisphere, brain stem, spinal cord, there were no cases of 1), and 2) 3) were the main cases. It is important in surgical selection to note that these cases generally have a more favorable prognosis compared to the adult type and have usefulness in diagnosing MAPK pathway abnormalities leading to the selection of molecularly targeted drugs. 3) includes pilocytic astrocytoma, subependymal giant cell astrocytoma, and pleomorphic xanthoastrocytoma. Among these, in the treatment of pilocytic astrocytomas located in the optic pathway and hypothalamus, biopsy becomes necessary for molecular diagnosis and the selection of appropriate therapeutic agents. Conversely, for unilateral optic nerve gliomas, options other than resection may be considered. 4) is primarily associated with epilepsy-related tumors. Surgical resection holds the promise of controlling epilepsy in these cases. However, various genetic abnormalities have been identified, which could prove useful in diagnosis and treatment. CONCLUSION Based on the new WHO classification, a reevaluation of treatment strategies for pediatric brain tumors is necessary.
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