[Efficacy of decitabine combined with low dose chemotherapy on children with acute myeloid leukemia].

L Y Fan, L Gao, D X Hu, J Ling, P F Xiao, H L He, Y Wang, J Li, J Lu, J Pan, S Y Hu
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Abstract

Objective: To evaluate the efficacy of decitabine combined with low dose chemotherapy (LDC) in the treatment of high-risk, refractory and relapsed pediatric acute myeloid leukemia (AML). Methods: Clinical data of 19 AML children treated with decitabine combined with LDC in the Department of Hematology, Children's Hospital of Soochow University from April 2017 to November 2019 were analyzed retrospectively. The therapeutic response, adverse effects and survival status were analyzed,and the outcomes of patients were followed up. Results: Among 19 AML cases, there were 10 males and 9 females. Five cases were high-risk AML, 7 cases were refractory AML, and 7 cases were relapsed AML. After one course of decitabine+LDC treatment, 15 cases achieved complete remission, 3 cases got partial remission, and only 1 case didn't get remission. All patients received allogeneic hematopoietic stem cell transplantation as consolidation therapy. The follow-up time of all cases was 46 (37, 58) months, 14 children had survived. The cumulative three-year overall survival rate was (79±9) %, events free survival rates was (68±11) %, and recurrence free survival rate was (81±10) %. The most common adverse effects related to the induction treatment were cytopenia (19 cases) and infection (16 cases).There were no treatment-related death during the therapy. Conclusion: Decitabine combined with LDC is a safe and effective option for high-risk, refractory and relapsed AML children, which provides an opportunity for HSCT.

【地西他滨联合小剂量化疗治疗儿童急性髓性白血病疗效观察】。
目的:评价地西他滨联合低剂量化疗(LDC)治疗高危、难治、复发儿童急性髓性白血病(AML)的疗效。方法:回顾性分析2017年4月至2019年11月苏州大学儿童医院血液科应用地西他滨联合LDC治疗的19例AML患儿的临床资料。分析两组患者的治疗效果、不良反应及生存状况,并对患者结局进行随访。结果:19例AML患者中,男性10例,女性9例。高危AML 5例,难治性AML 7例,复发性AML 7例。地西他滨+LDC治疗1个疗程后,完全缓解15例,部分缓解3例,未缓解1例。所有患者均接受同种异体造血干细胞移植作为巩固治疗。所有病例随访46(37,58)个月,14例患儿存活。累计三年总生存率为(79±9)%,无事件生存率为(68±11)%,无复发生存率为(81±10)%。诱导治疗最常见的不良反应是细胞减少(19例)和感染(16例)。治疗期间无治疗相关死亡。结论:地西他滨联合LDC治疗高危、难治性、复发性AML患儿安全有效,为HSCT的开展提供了契机。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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