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儿童不可切除及复发性髓内神经胶质瘤的化疗。法国儿科肿瘤学会(SFOP)脑肿瘤小组委员会

Chemotherapy for unresectable and recurrent intramedullary glial tumours in children. Brain Tumours Subcommittee of the French Society of Paediatric Oncology (SFOP).

作者信息

Doireau V, Grill J, Zerah M, Lellouch-Tubiana A, Couanet D, Chastagner P, Marchal J C, Grignon Y, Chouffai Z, Kalifa C

机构信息

Department of Paediatrics, Gustave Roussy Institute, Villejuif, France.

出版信息

Br J Cancer. 1999 Nov;81(5):835-40. doi: 10.1038/sj.bjc.6690772.

Abstract

Adjuvant treatment for intramedullary tumours is based on radiotherapy. The place of chemotherapy in this setting has yet to be determined. Between May 1992 and January 1998, eight children with unresectable or recurrent intramedullary glioma were treated with the BB SFOP protocol (a 16-month chemotherapy regimen with carboplatin, procarbazine, vincristine, cyclophosphamide, etoposide and cisplatin). Six children had progressive disease following incomplete surgery and two had a post-operative relapse. Three patients had leptomeningeal dissemination at the outset of chemotherapy. Seven of the eight children responded clinically and radiologically, while one remained stable. At the end of the BB SFOP protocol four children were in radiological complete remission. After a median follow-up of 3 years from the beginning of chemotherapy, all the children but one (who died from another cause) are alive. Five patients remain progression-free, without radiotherapy, 59, 55, 40, 35 and 16 months after the beginning of chemotherapy. The efficacy of this chemotherapy in patients with intramedullary glial tumours calls for further trials in this setting, especially in young children and patients with metastases.

摘要

髓内肿瘤的辅助治疗以放疗为基础。化疗在这种情况下的作用尚未确定。1992年5月至1998年1月期间,8名患有不可切除或复发性髓内胶质瘤的儿童接受了BB SFOP方案治疗(一种为期16个月的化疗方案,使用卡铂、丙卡巴肼、长春新碱、环磷酰胺、依托泊苷和顺铂)。6名儿童在不完全手术后病情进展,2名儿童术后复发。3名患者在化疗开始时已有软脑膜播散。8名儿童中有7名在临床和影像学上有反应,1名病情稳定。在BB SFOP方案结束时,4名儿童达到影像学完全缓解。从化疗开始起中位随访3年后,除1名儿童(死于其他原因)外,所有儿童均存活。5名患者在化疗开始后59、55、40、35和16个月时未接受放疗且无疾病进展。这种化疗对髓内胶质瘤患者的疗效需要在这种情况下进行进一步试验,尤其是在幼儿和有转移的患者中。

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