Borg Martin
Department of Radiation Oncology, Royal Adelaide Hospital, Adelaide, South Australia.
Med Pediatr Oncol. 2003 Jun;40(6):367-74. doi: 10.1002/mpo.10285.
Primary germ cell tumours (GCT) of the central nervous system (CNS) are rare tumours of children and adults. As few prospective, randomised trials have been published, management decisions are often based on retrospective and historical studies, histology, age, performance status, and extent of disease at diagnosis. This article reviews the current controversies in the radiotherapeutic management of primary GCT of the CNS.
A computerised literature search was performed using the Medline database from 1975 to 2000, this being limited to publications written in the English language on CNS GCT in children up to the age of 16 years.
Issues in radiation therapy currently undergoing review include the role of cranio-spinal irradiation (CSI), radiation therapy field sizes, the radiation therapy dose, the extent of surgery in combination with radiotherapy, and the role and timing of chemotherapy in combination with radiotherapy.
The excellent outcome in children with pure germinoma of the CNS and the long-term morbidity associated with standard therapy justifies attempts to limit both the total radiation dose and field sizes, with or without the addition of chemotherapy. The poorer outcome associated with non-germinoma GCT justifies a more aggressive approach in children, combining chemotherapy, surgery and virgule, or radiation therapy, based on known prognostic factors.
中枢神经系统(CNS)原发性生殖细胞肿瘤(GCT)在儿童和成人中均属罕见肿瘤。由于已发表的前瞻性随机试验较少,治疗决策往往基于回顾性和历史性研究、组织学、年龄、体能状态以及诊断时的疾病范围。本文综述了中枢神经系统原发性GCT放射治疗管理方面当前存在的争议。
利用Medline数据库对1975年至2000年的文献进行计算机检索,检索限于16岁以下儿童中枢神经系统GCT的英文出版物。
目前正在重新审视的放射治疗问题包括全脑脊髓照射(CSI)的作用、放射治疗野大小、放射治疗剂量、与放射治疗联合的手术范围以及化疗与放射治疗联合的作用和时机。
中枢神经系统纯生殖细胞瘤患儿的良好预后以及标准治疗相关的长期发病率,证明无论是否加用化疗,都应尝试限制总放射剂量和照射野大小。非生殖细胞瘤性GCT的较差预后证明对儿童采取更积极的治疗方法是合理的,即根据已知的预后因素,联合化疗、手术和/或放射治疗。