髓母细胞瘤:目前的观点和最新进展。

Jung Yoon Choi
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摘要

髓母细胞瘤是儿童时期最常见的中枢神经系统胚胎性肿瘤。包括手术、放疗和化疗在内的多模式联合治疗方法改善了髓母细胞瘤的预后。基因组研究的进展表明,髓母细胞瘤不是一个生物学或临床分离的实体。以前,风险是根据组织学、转移的存在、切除程度和诊断时的年龄来划分的。通过整合基因组学的发展,最近提出了新的基于生物学的风险分层方法。了解髓母细胞瘤患者的遗传易感性也很重要。因此,治疗目标是提高生存率,减少额外的不良反应和减少长期的后遗症。有必要将遗传发现纳入护理标准,并进行反映这一点的临床试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Medulloblastoma: Current Perspectives and Recent Advances.

Medulloblastoma is the most common embryonal tumor of the central nervous system in childhood. Combined multimodality approaches, including surgery, radiation, and chemotherapy, have improved the outcome of medulloblastoma. Advances in genomic research have shown that medulloblastoma is not a biologically or clinically discrete entity. Previously, the risk was divided according to histology, presence of metastasis, degree of resection, and age at diagnosis. Through the development of integrated genomics, new biology-based risk stratification methods have recently been proposed. It is also important to understand the genetic predisposition of patients with medulloblastoma. Therefore, treatment goal aimed to improve the survival rate with minimal additional adverse effects and reduced long-term sequelae. It is necessary to incorporate genetic findings into the standard of care, and clinical trials that reflect this need to be conducted.

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