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儿童急性白血病的异基因骨髓移植:采用分次全身照射、大剂量依托泊苷和环磷酰胺进行细胞减灭。

Allogeneic bone marrow transplantation for children with acute leukemia: cytoreduction with fractionated total body irradiation, high-dose etoposide and cyclophosphamide.

作者信息

Duerst R E, Horan J T, Liesveld J L, Abboud C N, Zwetsch L M, Senf E S, Constine L S, Raubertas R F, Passarell J A, DiPersio J F

机构信息

Department of Pediatrics, University of Rochester, School of Medicine and Dentistry, Rochester, NY 14642, USA.

出版信息

Bone Marrow Transplant. 2000 Mar;25(5):489-94. doi: 10.1038/sj.bmt.1702181.

Abstract

Marrow-ablative chemo-radiotherapy followed by hematopoietic stem cell rescue from an allogeneic source improves outcomes for children with high-risk acute leukemia. The first effective pre-transplant preparative regimens consisted of high-dose cyclophosphamide (CY) and total body irradiation (TBI). Subsequent attempts have been made to improve leukemia-free survival, by adding other chemotherapy agents to these agents. In previous clinical studies of total body irradiation, etoposide, cyclophosphamide (TBI-VP-16-Cy) in adult allogeneic bone marrow transplantation, there has been a high incidence of severe regimen-related toxicity. In this study, we investigated the safety and efficacy of this combination in 41 children who received TBI (12-14 Gy), VP-16 (30 mg/kg), and CY (60 mg/kg x 2) and then either matched sibling or alternative donor transplants for acute leukemia. There was only one case of fatal regimen-related toxicity. The estimated 3-year event-free survival for patients with early or intermediate stage disease was 68% (53-88%). The estimated event-free survival of patients with advanced disease was 17% (5-59%). TBI-VP16-CY is safe in pediatric transplantation, and it has good efficacy for transplant recipients with less advanced disease. Bone Marrow Transplantation (2000) 25, 489-494.

摘要

清髓性放化疗后接受异基因来源的造血干细胞救援可改善高危急性白血病患儿的预后。首个有效的移植前预处理方案由大剂量环磷酰胺(CY)和全身照射(TBI)组成。后续尝试通过在这些药物中添加其他化疗药物来提高无白血病生存率。在先前关于成人异基因骨髓移植中全身照射、依托泊苷、环磷酰胺(TBI-VP-16-Cy)的临床研究中,严重的方案相关毒性发生率很高。在本研究中,我们调查了41例接受TBI(12 - 14 Gy)、VP-16(30 mg/kg)和CY(60 mg/kg×2),然后接受匹配同胞或替代供体移植治疗急性白血病的儿童中该联合方案的安全性和有效性。仅有1例致命的方案相关毒性病例。早期或中期疾病患者的估计3年无事件生存率为68%(53 - 88%)。晚期疾病患者的估计无事件生存率为17%(5 - 59%)。TBI-VP16-CY在儿科移植中是安全的,并且对病情不太严重的移植受者具有良好的疗效。《骨髓移植》(2000年)第25卷,第489 - 494页

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