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诊断时年龄超过1岁的IV期神经母细胞瘤患者:对反应不佳者采用白消安、环磷酰胺和马法兰联合巩固治疗,随后进行体外美法仑净化的自体骨髓移植。

Stage IV neuroblastoma in patients over 1 year of age at diagnosis: consolidation of poor responders with combined busulfan, cyclophosphamide and melphalan followed by in vitro mafosfamide-purged autologous bone marrow transplantation.

作者信息

Hartmann O, Valteau-Couanet D, Benhamou E, Vassal G, Rubie H, Beaujean F, Lemerle J

机构信息

Paediatric Department, Institut Gustave Roussy, Villejuif, France.

出版信息

Eur J Cancer. 1997 Oct;33(12):2126-9. doi: 10.1016/s0959-8049(97)00227-x.

DOI:10.1016/s0959-8049(97)00227-x
PMID:9516867
Abstract

In an attempt to improve the poor prognosis of poor responders with stage IV neuroblastoma, a new combined high-dose chemotherapy conditioning regimen was tested. Event-free and overall survival, as well as the incidence of complications, were analysed. Twenty-five children aged 12-146 months at diagnosis entered this study. All were in complete remission (CR) at the time of high-dose chemotherapy. Two or three different protocols had been necessary for them to achieve a CR. High-dose chemotherapy consisted of a combination of busulfan (600 mg/m2), cyclophosphamide (4400 mg/m2) and melphalan (140 mg/m2). It was followed by autologous bone marrow transplantation (ABMT). The bone marrow graft was purged in vitro with mafosfamide. The probability of event-free survival (EFS) at 5 years post-ABMT was 34%, compared to < 8% in a historical series. Toxicity was severe but manageable and 2 complication-related deaths were observed. Veno-occlusive disease was the most frequent extrahaematopoietic complication encountered, but its outcome was always favourable. By using a very intensive conditioning regimen consisting of a combination of three alkylating agents, the EFS of poor responders with metastatic neuroblastoma was improved and similar to that of good responders. When compared with a previously published similar series of patients, the improvement in survival appears probably related to intensification of the conditioning regimen.

摘要

为改善IV期神经母细胞瘤低反应者的不良预后,对一种新的联合大剂量化疗预处理方案进行了测试。分析了无事件生存期和总生存期以及并发症的发生率。25名诊断时年龄在12至146个月的儿童进入了本研究。所有患儿在接受大剂量化疗时均处于完全缓解(CR)状态。他们需要两到三种不同的方案才能达到CR。大剂量化疗包括白消安(600mg/m²)、环磷酰胺(4400mg/m²)和美法仑(140mg/m²)的联合应用。随后进行自体骨髓移植(ABMT)。骨髓移植物在体外使用马磷酰胺进行净化处理。ABMT后5年的无事件生存率(EFS)为34%,而历史队列中的这一比例小于8%。毒性严重但可控,观察到2例与并发症相关的死亡。静脉闭塞性疾病是最常见的造血系统外并发症,但其预后总是良好的。通过使用由三种烷化剂联合组成的非常强化的预处理方案,转移性神经母细胞瘤低反应者的EFS得到了改善,与高反应者相似。与先前发表的类似患者系列相比,生存改善可能与预处理方案的强化有关。

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引用本文的文献

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