首页> 外文期刊>British Journal of Haematology >Allogeneic haematopoietic stem cell transplantation for infant acute lymphoblastic leukaemia with KMT2A (MLL) rearrangements: a retrospective study from the paediatric acute lymphoblastic leukaemia working group of the Japan Society for Haematopoietic Cell Transplantation
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Allogeneic haematopoietic stem cell transplantation for infant acute lymphoblastic leukaemia with KMT2A (MLL) rearrangements: a retrospective study from the paediatric acute lymphoblastic leukaemia working group of the Japan Society for Haematopoietic Cell Transplantation

机译:伴有KMT2A(MLL)重排的婴儿急性淋巴细胞白血病同种异体造血干细胞移植:来自日本造血细胞移植学会小儿急性淋巴细胞白血病工作组的回顾性研究

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摘要

Allogeneic haematopoietic stem cell transplantation (HSCT) is still considered to play an important role as a consolidation therapy for high-risk infants with acute lymphoblastic leukaemia (ALL). Here, we retrospectively analysed outcomes of HSCT in infants with ALL based on nationwide registry data of the Japan Society for Haematopoietic Cell Transplantation. A total of 132 allogeneic HSCT for infant ALL with KMT2A (MLL) gene rearrangements, which were performed in first complete remission (CR1), were analysed. The 5-year overall survival rate after transplantation was 674 +/- 45%). Although recent HSCT (after 2004) had a trend toward better survival, no statistical correlation was observed between outcomes and each factor, including age at diagnosis, initial leucocyte count, cytogenetics, donor types or conditioning of HSCT. Myeloablative conditioning with total body irradiation did not provide a better survival (607 +/- 92%) over that with busulfan (BU; 678 +/- 57%). Two of the 28 patients treated with irradiation, but none of the 90 BU-treated patients, developed a secondary malignant neoplasm. In conclusion, allogeneic HSCT using BU was a valuable option for infant ALL with KMT2A rearrangements in CR1.
机译:异基因造血干细胞移植(HSCT)仍被认为在合并急性淋巴细胞白血病(ALL)的高危婴儿中起着重要的治疗作用。在此,我们根据日本造血细胞移植学会的全国注册数据回顾性分析了ALL患儿的HSCT结果。分析了在首次完全缓解(CR1)中进行的132例针对患有KMT2A(MLL)基因重排的婴儿ALL的同种异体HSCT。移植后的5年总生存率为674 +/- 45%。尽管最近的HSCT(2004年以后)有更好的生存趋势,但结局与每个因素(包括诊断时的年龄,初始白细胞计数,细胞遗传学,供体类型或HSCT条件)之间均未观察到统计学相关性。全身照射的清髓性调理不能提供比白消安(BU; 678 +/- 57%)更好的存活率(607 +/- 92%)。在接受放射线治疗的28例患者中,有2例发生了继发性恶性肿瘤,但90例BU治疗的患者中均没有。总之,使用BU的异基因HSCT对于CR1中KMT2A重排的婴儿ALL是一个有价值的选择。

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