成人成神经管细胞瘤治疗的当前和未来策略。

Forum (Genoa, Italy) Pub Date : 2003-01-01
R D Kortmann, A A Brandes
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引用次数: 0

摘要

成人髓母细胞瘤是罕见的,在肿瘤部位(半球位置)、组织学亚型(结缔组织增生变异)、转移扩散发生率较低和频繁的晚期复发方面与儿童髓母细胞瘤不同。在儿童中,转移性疾病的存在具有重要的预后意义。不同的组织学亚型和分子遗传/生物学标记的作用尚不清楚,值得进一步研究。治疗策略基本上是基于儿童髓母细胞瘤的经验。手术后对整个中枢神经系统进行照射,然后对后窝进行刺激是治疗的基础。充分的剂量处方和高质量的治疗是最佳肿瘤控制的先决条件。与儿童不同,化疗的作用是一个悬而未决的问题,需要前瞻性的研究。即将进行的eortc研究正在解决这个问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Current and future strategies in the management of medulloblastoma in adults.

Medulloblastoma in adults are rare and differ from their childhood counterparts in terms of tumor site (hemispheric location), histological subtype (desmoplastic variant), lower incidence of metastatic spread and frequent late relapses. As in children the presence of metastatic disease is of major prognostic significance. The role of different histological subtypes and molecular genetic/biological markers is unknown and deserves further investigations. The therapeutic strategies are essentially based on experiences in childhood medulloblastomas. Surgery followed by irradiation of the entire central nervous system followed by a boost to the posterior fossa is the cornerstones of treatment. A sufficient dose prescription and a high quality of treatment are a prerequisite for an optimal tumor control. Unlike in children the role of chemotherapy is an open question and requires prospective investigations. The forthcoming EORTC-study is addressing this issue.

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