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大剂量疗法对处于完全缓解期的高危尤因肉瘤患儿的影响:来自欧洲血液与骨髓移植协会实体瘤登记处的报告

Impact of megatherapy in children with high-risk Ewing's tumours in complete remission: a report from the EBMT Solid Tumour Registry.

作者信息

Ladenstein R, Lasset C, Pinkerton R, Zucker J M, Peters C, Burdach S, Pardo N, Dallorso S, Coze C

机构信息

St Anna Children's Hospital, Vienna, Austria.

出版信息

Bone Marrow Transplant. 1995 May;15(5):697-705.

PMID:7670398
Abstract

The European BMT Solid Tumour Registry (EBMT-STR) received reports from 21 European transplant centers on 63 patients (50 Ewing's sarcomas and 13 peripheral neuroectodermal tumours) in first (n = 32) or second CR (n = 31) consolidated with megatherapy and BM and/or PSC rescue between December 1982 and November 1992. There were 31 males and 32 females with a median age of 12 years (range 1-30 years) at megatherapy. The median follow-up time since megatherapy is 4 years (range 1 month to 10 years), Thirty-two patients with metastatic disease at diagnosis (22 had metastases to the bone and/or bone marrow) and consolidated in CR1 reached an actuarial event-free survival (EFS) of 21% at 5 years. Thirty one patients in CR2 achieved an actuarial EFS of 32% at 5 years. Favourable outcome was limited to relapse patients with localised disease at initial diagnosis. Distant relapse had a more favourable prognosis than local failure. Analysis of the different megatherapy strategies could not identify a significantly superior approach, nor is there convincing evidence in favour of double graft procedures. From the above results it appears that consolidation treatment by megatherapy contributes to improved EFS rates in high-risk patients compared with historical experience. Major questions for the future to be addressed prior to randomised studies include agreement on the definition of high-risk patients and the most efficient megatherapy procedure.

摘要

欧洲骨髓移植实体瘤登记处(EBMT-STR)收到了21个欧洲移植中心提交的报告,这些报告涉及1982年12月至1992年11月期间接受大剂量疗法联合骨髓和/或外周血干细胞救援进行巩固治疗的63例患者(50例尤因肉瘤和13例外周神经外胚层肿瘤),其中处于首次完全缓解(n = 32)或第二次完全缓解(n = 31)。进行大剂量疗法时,有31名男性和32名女性,中位年龄为12岁(范围1 - 30岁)。自大剂量疗法后的中位随访时间为4年(范围1个月至10年)。32例诊断时患有转移性疾病(22例有骨和/或骨髓转移)且在首次完全缓解时进行巩固治疗的患者,其5年无事件生存率(EFS)为21%。31例处于第二次完全缓解的患者5年的精算EFS为32%。良好的预后仅限于初始诊断为局限性疾病的复发患者。远处复发的预后比局部失败更有利。对不同大剂量疗法策略的分析未能确定一种明显更优的方法,也没有令人信服的证据支持双重移植程序。从上述结果来看,与历史经验相比,大剂量疗法的巩固治疗有助于提高高危患者的EFS率。在进行随机研究之前,未来需要解决的主要问题包括就高危患者的定义和最有效的大剂量疗法程序达成一致。

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