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地西他滨与阿糖胞苷、阿克拉霉素及粒细胞集落刺激因子联合方案成功治疗老年慢性粒-单核细胞白血病转化的急性髓系白血病:一例报告

Successful management of acute myeloid leukemia transformed from chronic myelomonocytic leukemia in the elderly by a combination regimen of decitabine and cytarabine, aclarubicin and granulocyte colony-stimulating factor: A case report.

作者信息

Deng Qi, Li Jing-Yi, Liu Peng-Jiang, Zhao Ming-Feng

机构信息

Department of Hematology, The First Central Hospital of Tianjin, Tianjin 300192, P.R. China.

出版信息

Oncol Lett. 2015 Mar;9(3):1217-1220. doi: 10.3892/ol.2015.2870. Epub 2015 Jan 13.

Abstract

Despite advances in the treatment of acute myeloid leukemia (AML) in recent years, the outcome of elderly AML patients with antecedent hematological disorders remains unsatisfactory. The present study describes a case of complete remission in an elderly patient with AML transformed from chronic myelomonocytic leukemia (CMML) and the treatment of the case with decitabine in combination with cytarabine, aclarubicin and granulocyte colony-stimulating factor (CAG). A 70-year-old male was admitted with fever, pruritus and weakness that had been apparent for two weeks, and a two-year history of monocytosis (22.5-27.0%). Further examinations revealed a hemoglobin level of 106 g/l, a white blood cell count of 39.52×10/l, a platelet count of 81×10/l, Y chromosome loss and uniparental disomy on chromosomes 4q, 2q and 19p. The patient was diagnosed with AML transformed from CMML, with cytogenetic anomalies. A combination regimen of decitabine and CAG was administered. Subsequent to one cycle, the patient achieved complete remission. The patient was then followed up with three courses of the same regimen and achieved clinical remission, with no evidence of AML relapse. The present study suggests that a combination of low-dose decitabine and CAG may offer a novel and potentially effective treatment regimen for elderly AML patients.

摘要

尽管近年来急性髓系白血病(AML)的治疗取得了进展,但患有前驱血液系统疾病的老年AML患者的治疗结果仍不尽人意。本研究描述了一例由慢性粒单核细胞白血病(CMML)转化而来的老年AML患者完全缓解的病例,以及用地西他滨联合阿糖胞苷、阿克拉霉素和粒细胞集落刺激因子(CAG)治疗该病例的情况。一名70岁男性因发热、瘙痒和乏力入院,这些症状已持续两周,并有两年单核细胞增多症病史(22.5%-27.0%)。进一步检查显示血红蛋白水平为106g/l,白细胞计数为39.52×10⁹/l,血小板计数为81×10⁹/l,Y染色体缺失以及4号染色体长臂、2号染色体长臂和19号染色体短臂单亲二体。该患者被诊断为CMML转化的AML,伴有细胞遗传学异常。给予地西他滨和CAG联合方案治疗。一个疗程后,患者实现完全缓解。随后对患者进行相同方案的三个疗程随访,实现临床缓解,无AML复发迹象。本研究表明,低剂量地西他滨和CAG联合可能为老年AML患者提供一种新的、潜在有效的治疗方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e167/4315126/0beffe02a866/OL-09-03-1217-g00.jpg

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