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1070例采用干细胞救援的神经母细胞瘤清髓大剂量治疗程序:17年的欧洲经验及结论。欧洲血液和骨髓移植登记处实体瘤工作组

1070 myeloablative megatherapy procedures followed by stem cell rescue for neuroblastoma: 17 years of European experience and conclusions. European Group for Blood and Marrow Transplant Registry Solid Tumour Working Party.

作者信息

Philip T, Ladenstein R, Lasset C, Hartmann O, Zucker J M, Pinkerton R, Pearson A D, Klingebiel T, Garaventa A, Kremens B, Bernard J L, Rosti G, Chauvin F

机构信息

Centre Léon Bérard, Department of Paediatrics, Lyon, France.

出版信息

Eur J Cancer. 1997 Oct;33(12):2130-5. doi: 10.1016/s0959-8049(97)00324-9.

Abstract

1070 myeloablative procedures followed by stem cell rescue for neuroblastoma are reviewed. These 1070 procedures are part of the European Group for Blood and Marrow Transplant (EBMTG) registry from the last 17 years (in 4536 patients). In 1070 neuroblastoma patients, survival at 2 years was 49%, at 5 years, 33% and relapses were observed as late as 7 years post-BMT (bone marrow transplant). However, 5-year survivors after megatherapy with BMT for stage 4 disease do have an 80% chance of becoming a long-term survivor. When BMT had been used in first complete response (CR1) no salvage was possible, whereas 15% survivors may be seen if BMT is used for the first time at relapse. Infants with stage 4 neuroblastoma had a 17% toxic death rate and indication in this group is exceptional and not recommended. In a matched cohort (17 allogeneic and 34 autologous), autologous stem cell rescue (SCR) was shown to be at least equal to allogeneic SCR. Multivariate analysis of clinical prognostic factors in children with stage 4 disease over 1 year showed that event-free survival was mainly influenced by two adverse factors before the megatherapy procedure: persisting skeleton lesions (99Tc and/or mIBG scan positive) as well as persisting bone marrow (BM) involvement.

摘要

对1070例采用干细胞救援治疗神经母细胞瘤的清髓性治疗程序进行了回顾。这1070例治疗程序是欧洲血液和骨髓移植组(EBMTG)过去17年登记数据的一部分(共4536例患者)。在1070例神经母细胞瘤患者中,2年生存率为49%,5年生存率为33%,且在骨髓移植(BMT)后7年仍观察到复发情况。然而,对于4期疾病采用大剂量治疗联合BMT后的5年幸存者,有80%的机会成为长期幸存者。当BMT用于首次完全缓解期(CR1)时,无法进行挽救治疗,而如果在复发时首次使用BMT,则可能有15%的幸存者。4期神经母细胞瘤婴儿的毒性死亡率为17%,该组的适应症极为罕见且不推荐。在一个匹配队列(17例异基因和34例自体)中,自体干细胞救援(SCR)显示至少与异基因SCR相当。对1岁以上4期疾病儿童的临床预后因素进行多变量分析显示,无事件生存期主要受大剂量治疗程序前两个不利因素的影响:持续的骨骼病变(99Tc和/或mIBG扫描阳性)以及持续的骨髓受累。

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