HLA haploidentical hematopoietic cell transplantation using clofarabine and busulfan for refractory pediatric hematological malignancy.

HLA haploidentical hematopoietic cell transplantation using clofarabine and busulfan for refractory pediatric hematological malignancy.
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使用氯法拉滨和白消安进行 HLA 单倍相合造血细胞移植治疗难治性儿科血液恶性肿瘤。

DOI:
10.1007/s12185-017-2187-3
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发表时间:
2017
期刊:
影响因子:
2.1
通讯作者:
Morio T.
Morio T.
中科院分区:
医学4区
文献类型:
--
作者:
Takagi M;Ishiwata Y;Aoki Y;Miyamoto S;Hoshino A;Matsumoto K;Nishimura A;Tanaka M;Yanagimachi M;Mitsuiki N;Imai K;Kanegane H;Kajiwara M;Takikawa K;Mae T;Tomita O;Fujimura J;Yasuhara M;Tomizawa D;Mizutani S;Morio T.

文献摘要

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本研究对3例难治性儿童白血病患者进行了单倍体造血细胞移植(HCT)调节,采用氯法拉滨和基于血药浓度-时间曲线(AUC)的靶区调节。2例已接受多次移植患者的目标AUC分别为3600 μmol min/L和4000 μmol min/L,唐氏综合征患者的目标AUC为3000 μmol min/L。在所有病例中,方案相关的毒性耐受良好。在整个随访期间(31 - 167周),三名患者均保持细胞学缓解。因此,对于复发性或难治性儿童白血病,单倍体HCT调节联合氯法拉滨和靶向auc的布苏凡调节可能是更好的选择。
Haploidentical hematopoietic cell transplantation (HCT) conditioning with clofarabine and target area under the blood concentration–time curve (AUC)-based busulfan adjustment was performed in three patients with refractory pediatric leukemia. The target AUC for two patients who had already received multiple transplantations was 3600 and 4000 μmol min/L, and that for the patient with Down’s syndrome was 3000 μmol min/L. Regimen-related toxicity was well tolerated in all cases. All three maintained cytological remission throughout the follow-up period (between 31 and 167 weeks). Thus, haploidentical HCT conditioning with clofarabine and target AUC-based busulfan adjustment may be a preferable option for children with recurrent or refractory pediatric leukemia.