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地西他滨联合中剂量阿糖胞苷治疗DEK/CAN阳性急性髓系白血病:一例报告

Decitabine combined with medium-dose cytarabine in the treatment of DEK/CAN-positive acute myeloid leukemia: a case report.

作者信息

Zhang Xueya, Zhang Xuezhi

机构信息

Department of Hematology, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, China.

Department of Neurosurgery, The First Affiliated Hospital of Nanchang University, Nanchang, China.

出版信息

Ann Palliat Med. 2021 Apr;10(4):4955-4958. doi: 10.21037/apm-19-379. Epub 2021 Apr 1.

Abstract

Acute myeloid leukemia (AML) is a malignant clonal hematopoietic stem cell disease. Although there are many therapeutic options, it is still an incurable hematological malignancy. Moreover, the prognosis of AML is closely related to its cytogenetics and molecular biology. The DEK/CAN fusion gene formed by t (6;9)(p23;q34) occurs with an incidence of 1-5% in adult patients with AML usually indicates a poor prognosis. Hematopoietic stem cell transplantation can prolong the disease-free survival rate of patients with AML positive for DEK/CAN fusion gene, and the development of new drugs is still one of the hotspots of clinical research. Herein, we reported the first case with DEK/CAN-positive AML who achieved complete remission of molecular biology via decitabine combined with a medium-dose cytarabine regimen. The patient has received three courses of intensive treatment with decitabine combined with medium-dose cytarabine regimen and maintain complete remission of molecular biology for up to 11 months. We hypothesized that the combination of decitabine and medium-dose cytarabine play an important role in targeting DEK/CAN and it should be verified by the accumulation of clinical cases and basic experiments in the future.

摘要

急性髓系白血病(AML)是一种恶性克隆性造血干细胞疾病。尽管有多种治疗选择,但它仍然是一种无法治愈的血液系统恶性肿瘤。此外,AML的预后与其细胞遗传学和分子生物学密切相关。由t(6;9)(p23;q34)形成的DEK/CAN融合基因在成年AML患者中的发生率为1%-5%,通常提示预后不良。造血干细胞移植可延长DEK/CAN融合基因阳性的AML患者的无病生存率,新药研发仍是临床研究的热点之一。在此,我们报告了首例通过地西他滨联合中剂量阿糖胞苷方案实现分子生物学完全缓解的DEK/CAN阳性AML患者。该患者接受了三个疗程的地西他滨联合中剂量阿糖胞苷强化治疗,分子生物学完全缓解持续长达11个月。我们推测地西他滨和中剂量阿糖胞苷的联合在靶向DEK/CAN方面发挥重要作用,未来应通过临床病例积累和基础实验加以验证。

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