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一名慢性粒单核细胞白血病患者对5-氮杂胞苷的异常反应。

An unusual response to 5-azacitidine by a patient with chronic myelomonocytic leukemia.

作者信息

Islam Anwarul

机构信息

Division of Hematology/Oncology, Department of Medicine Buffalo General Hospital Buffalo General Medical Center Buffalo New York USA.

出版信息

Clin Case Rep. 2023 Aug 2;11(8):e7748. doi: 10.1002/ccr3.7748. eCollection 2023 Aug.

Abstract

KEY CLINICAL MESSAGE

Hypomethylating agents may be useful in some but not all cases of myelodysplastic syndromes. In some versions of these conditions, this treatment may yield deleterious results.

ABSTRACT

Chronic myelomonocytic leukemia (CMML) is considered to be a heterogeneous group of hematopoietic neoplasms. Usually it shares the features of myeloproliferative neoplasms (MPN) and myelodysplastic syndromes (MDS) and is known as MDS/MPN. It occurs mostly in the elderly and has an inherent tendency to transform to acute myeloid leukemia. FDA has approved hypomethylating agents (HMAs) such as 5-azacitidine (AZA) and decitabine (DEC) for the treatment of this disorder. The extent of response rate to AZA varies considerably among patients. Our report describes a patient with CMML who not only did not respond to a conventional dose of intravenous (IV) therapy with AZA, but showed marked progression of the disease with the leucocyte count rising exponentially while undergoing the aforesaid treatment. We believe this is the first such case reported in the currently extant literature.

摘要

关键临床信息

低甲基化药物可能对某些但并非所有骨髓增生异常综合征病例有用。在这些病症的某些类型中,这种治疗可能会产生有害结果。

摘要

慢性粒单核细胞白血病(CMML)被认为是一组异质性造血肿瘤。它通常兼具骨髓增殖性肿瘤(MPN)和骨髓增生异常综合征(MDS)的特征,被称为MDS/MPN。它主要发生在老年人中,并且具有向急性髓系白血病转化的内在倾向。美国食品药品监督管理局(FDA)已批准低甲基化药物(HMA),如5-氮杂胞苷(AZA)和地西他滨(DEC)用于治疗这种疾病。患者对AZA的反应率差异很大。我们的报告描述了一名CMML患者,该患者不仅对常规剂量的AZA静脉治疗无反应,而且在接受上述治疗时疾病出现明显进展,白细胞计数呈指数级上升。我们认为这是目前现有文献中报道的首例此类病例。

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