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来那度胺联合地西他滨治疗一名5q缺失且原始细胞增多的骨髓增生异常综合征患者。

Lenalidomide Plus Decitabine Treatment in a Myelodysplastic Syndrome Patient With Deletion 5q and Excess Blasts.

作者信息

Serin Istemi, Eren Rafet, Dogu Mehmet Hilmi

机构信息

Department of Hematology, University of Health Science, Istanbul Training and Research Hospital, Istanbul, Turkey.

Department of Hematology, University of Health Science, Okmeydani Training and Research Hospital, Istanbul, Turkey.

出版信息

J Hematol. 2020 Apr;9(1-2):33-36. doi: 10.14740/jh618. Epub 2020 Apr 23.

Abstract

This is the first case of decitabine plus lenalidomide treatment for a myelodysplastic syndrome (MDS) patient with 5q deletion (del(5q)) and elevated number of blasts. Upon bone marrow aspiration and biopsy with conventional cytogenetical studies she was diagnosed with MDS with del(5q) and refractory anemia with excess blasts (RAEB-1). Decitabine was started at a daily dose of 20 mg/m 1 - 5 days and lenalidomide was started at daily doses of 10 mg 6 - 20 days a month. After two cycles, her hemoglobin level increased and transfusion dependency ceased. After four cycles, bone marrow aspiration showed blast ratio of < 5%. Decitabine and lenalidomide were applied for three more cycles. Decitabine was terminated after seven cycles and lenalidomide has been continued for 12 months. Latest blood values (February 2020) were as follows: white blood cells (WBCs) of 8,670/mm, neutrophil count of 3,470/mm, hemoglobin (Hb) level of 11.7 g/dL and platelet count of 203,000/mm, and the patient continues to follow-up without treatment. In conclusion, combination of lenalidomide and decitabine seems to be an effective treatment modality without notable side effects in MDS patients with del(5q) and excess blasts. The efficacy of this combination should be validated with studies including large patient groups and with longer follow-up periods.

摘要

这是首例使用地西他滨联合来那度胺治疗伴有5号染色体缺失(del(5q))且原始细胞数量升高的骨髓增生异常综合征(MDS)患者的病例。经骨髓穿刺、活检及常规细胞遗传学研究,她被诊断为伴有del(5q)的MDS及伴有过多原始细胞的难治性贫血(RAEB-1)。地西他滨以每日20 mg/m²的剂量在第1 - 5天使用,来那度胺以每日10 mg的剂量在每月第6 - 20天使用。两个周期后,她的血红蛋白水平升高,不再依赖输血。四个周期后,骨髓穿刺显示原始细胞比例<5%。地西他滨和来那度胺又应用了三个周期。七个周期后停用了地西他滨,来那度胺持续使用了12个月。最新的血液检查结果(2020年2月)如下:白细胞(WBC)8670/mm³,中性粒细胞计数3470/mm³,血红蛋白(Hb)水平11.7 g/dL,血小板计数203000/mm³,患者继续接受观察且未进行治疗。总之,来那度胺和地西他滨联合使用似乎是治疗伴有del(5q)及过多原始细胞的MDS患者的一种有效治疗方式,且无明显副作用。这种联合用药的疗效应通过纳入大样本患者群体并进行更长随访期的研究来验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b4e/7188382/dd881f2188a6/jh-09-033-g001.jpg

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