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:婴幼儿毒性淋巴细胞白血病的同种异体造血干细胞移植:日本儿科急性淋巴细胞白血病工作组的回顾性研究,呕血细胞移植

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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:同种异体造血干细胞移植(HSCT)仍被认为是作为具有急性淋巴细胞白血病(全部)的高危婴儿的固结疗法的重要作用。在这里,我们回顾性地分析了基于日本血产细胞移植的全国范围内的全国范围内的婴儿的HSCT结果。分析了婴儿的总共132个同种异体HSCT,其含有KMT2A(MLL)基因重排,其在首次完全缓解(CR1)中进行的重排。移植后的5年整体存活率为674 +/- 45%)。虽然最近的HSCT(2004年以后)具有更好的生存趋势,但在结果和每种因素之间没有观察到统计相关性,包括诊断年龄,初始白细胞计数,细胞遗传学,供体类型或HSCT调节。含有总体辐射的肌钙性调理没有通过Busulfan(Bu; 678 +/- 57%)提供更好的存活率(607 +/- 92%)。 28例患者中的两种患者治疗,但90例治疗患者都没有,也产生了继发性肿瘤。总之,使用BU的同种异体HSCT是婴儿在CR1中具有KMT2A重排的宝贵选择。

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