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Autologous purified peripheral blood SCT in childhood low-risk relapsed ALL.

机译:自体纯净的外周血SCT在儿童期低危ALL中复发。

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The treatment of childhood B-cell-precursor ALL after isolated-extramedullary or late relapse is controversial. Most approaches are based on chemotherapy or allogeneic transplantation. The aim of this report is to assess the long-term outcome of children with 'low-risk' relapsed ALL treated according to a prospective purified auto-transplantation protocol. From January 1997 to March 2004, at a single pediatric Center, 30 ALL consecutive children, lacking an HLA-identical sibling, were treated according to the autologous purified peripheral blood stem cell protocol after isolated-extramedullary (7) or late medullary (24) relapse. After the 'DIAVE' mobilizing regimen a median of 11.6 x 10(6)CD34+/Kg (range 3.9-27.4) were collected. Leukaphereses were depleted by 99% of CD19+cells (range 98-100) by means of a double step immunological purification. The conditioning regimen included TBI. No early severe complications nor transplant-related deaths occurred; late effects, as expected, mostly consisted in endocrinological issues and were assessed at a median follow-up of 8.5 years. Five-year-EFS and survival were 68.5% (s.e. 7.9) and 85.7% (s.e. 5.9), respectively, for the 35 eligible patients and 70.0% (s.e. 8.4) and 86.7% (s.e. 6.2) for the 30 patients actually transplanted as per protocol. The outcome of this series favorably compares with historical data regarding both autologous transplantation and standard salvage chemotherapy.
机译:孤立性硬脑膜外或晚期复发后儿童B细胞前体ALL的治疗存在争议。大多数方法基于化学疗法或异体移植。本报告的目的是评估根据前瞻性纯化自动移植方案治疗的“低危”复发性ALL儿童的远期结局。从1997年1月至2004年3月,在一个单独的儿科中心,对30例没有HLA相同同胞的连续儿童进行了分离自上髓外(7)或晚髓(24)的治疗,并根据自体纯化的外周血干细胞方案进行了治疗。复发。在“ DIAVE”动员方案后,收集了中位数11.6 x 10(6)CD34 + / Kg(范围3.9-27.4)。通过双步免疫纯化,白细胞减少了99%的CD19 +细胞(范围98-100)。调理方案包括TBI。没有发生早期严重并发症,也没有发生与移植相关的死亡;如预期的那样,后期影响主要是内分泌学问题,中位随访时间为8.5年。符合条件的35名患者的五年EFS和生存率分别为68.5%(se 7.9)和85.7%(se 5.9),而实际移植的30例患者的70.0%(se 8.4)和86.7%(se 6.2)。每个协议。该系列的结果与自体移植和标准挽救性化疗的历史数据相比具有优势。

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