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作 者:许国发[1] 陈婷 蔺诗佳 刘焕凤 邓天霞 高蕾 刘耀 张诚 高力 张曦 孔佩艳
机构地区:[1]重庆市涪陵中心医院血液科,重庆400800 [2]陆军军医大学第二附属医院新桥医院血液科
出 处:《临床血液学杂志》2018年第1期52-56,共5页Journal of Clinical Hematology
摘 要:骨髓增生异常综合征(myelodysplastic syndrome,MDS)转化的急性髓系白血病(acute myeloid leukemia,AML)完全缓解(CR)率低,约为36%,生存期短,预后差[1]。有研究报道19.2%32.0%的AML患者存在FLT3-ITD突变,其中AML-M3患者的阳性率最高,Acute myeloid leukemia(AML)transformed by myelodysplastic syndrome(MDS)has low complete remission,high risk of relapse,short survival time and poor prognosis.If the patients also with FLT3-ITD positive,the outcome will be worse,and the possibility of survival is very low,even after allogeneic hematopoietic stem cell transplantation(Allo-HSCT).In this paper a 44 year old female patient with FLT3-ITD+AML-M5,transformed by MDS treated in our department were reported.The patient received chemotherapy with decitabine before and unrelated donor Allo-HSCT,and maintenance therapy of small dose of decitabine after HSCT.The early relapse after transplantation was successfully controlled,and the life of the patient had been over 2 years.
关 键 词:FLT3-ITD阳性 急性髓系白血病 骨髓增生异常综合征 地西他滨 异基因造血干细胞移植 无关供者
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