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MLL-AF4阳性急性淋巴细胞白血病非婴幼儿患者的良好预后:来自东京儿童癌症研究组的报告

Favorable outcome in non-infant children with MLL-AF4-positive acute lymphoblastic leukemia: a report from the Tokyo Children's Cancer Study Group.

作者信息

Tomizawa Daisuke, Kato Motohiro, Takahashi Hiroyuki, Fujimura Junya, Inukai Takeshi, Fukushima Takashi, Kiyokawa Nobutaka, Koh Katsuyoshi, Manabe Atsushi, Ohara Akira

机构信息

Division of Leukemia and Lymphoma, Children's Cancer Center, National Center for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo, 157-8535, Japan.

Division of Transplantation and Cell Therapy, Children's Cancer Center, National Center for Child Health and Development, Tokyo, Japan.

出版信息

Int J Hematol. 2015 Nov;102(5):602-10. doi: 10.1007/s12185-015-1869-y. Epub 2015 Sep 26.

Abstract

Unlike acute lymphoblastic leukemia (ALL) in infants, MLL gene rearrangement (MLL-r) is rare in ALL children (≥1 year old). The outcome and optimal treatment options for MLL-r ALL remain controversial. Among the 1827 children enrolled in the Tokyo Children's Cancer Study Group ALL studies L95-14, L99-15, L99-1502, L04-16, and L07-1602 (1995-2009), 25 MLL-r ALL patients (1.3 %) were identified. Their median age and leukocyte count at diagnosis was 2 years old (range 1-15 years) and 27,690/μL (range 1800-1,113,000/μL), respectively. All but one patient achieved complete remission (CR) after induction therapy, and 19 underwent allogeneic hematopoietic stem cell transplantation (HSCT) in first CR according to the protocol. The 5-year event-free survival (EFS) and overall survival (OS) rate were 60.0 % [standard error (SE), 9.7 %] and 64.0 % (SE 9.6 %), respectively. Notably, 9/12 cases with MLL-AF4-positive ALL are alive in continuous CR with a 75.0 % (SE 12.5 %) EFS rate. The causes of treatment failure were as follows: one induction failure, five relapses, and five transplant-related deaths. With intensive chemotherapy and allogeneic HSCT, favorable outcome of children (≥1 year old) with MLL-AF4-positive ALL was observed. However, considering the risk of acute and late toxicities associated with HSCT, its indication should be restricted.

摘要

与婴儿急性淋巴细胞白血病(ALL)不同,MLL基因重排(MLL-r)在儿童ALL(≥1岁)中很少见。MLL-r ALL的预后和最佳治疗方案仍存在争议。在东京儿童癌症研究组ALL研究L95-14、L99-15、L99-1502、L04-16和L07-1602(1995 - 2009年)纳入的1827名儿童中,确定了25例MLL-r ALL患者(1.3%)。他们诊断时的中位年龄和白细胞计数分别为2岁(范围1 - 15岁)和27,690/μL(范围1800 - 1,113,000/μL)。除1例患者外,所有患者诱导治疗后均达到完全缓解(CR),19例根据方案在首次CR时接受了异基因造血干细胞移植(HSCT)。5年无事件生存率(EFS)和总生存率(OS)分别为60.0%[标准误差(SE),9.7%]和64.0%(SE 9.6%)。值得注意的是,12例MLL-AF4阳性ALL患者中有9例持续CR存活,EFS率为75.0%(SE 12.5%)。治疗失败的原因如下:1例诱导失败、5例复发和5例移植相关死亡。通过强化化疗和异基因HSCT,观察到MLL-AF4阳性ALL儿童(≥1岁)的良好预后。然而,考虑到与HSCT相关的急性和晚期毒性风险,其适应证应受到限制。

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