一名低危骨髓增生异常综合征患者接受阿扎胞苷治疗后的长期血液学反应:病例报告

IF 0.7 Q4 HEMATOLOGY Leukemia Research Reports Pub Date : 2024-01-01 DOI:10.1016/j.lrr.2024.100412
Konstantinos Loukidis , Marcel Tschopp
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引用次数: 0

摘要

我们报告了一名 65 岁低风险骨髓增生异常综合征和多系发育不良患者接受低甲基化药物治疗的结果。在促红细胞生成素和沙利度胺治疗失败后,患者接受了阿扎胞苷治疗,并在95个月内实现了血液学缓解。2016年,患者改用地西他滨治疗,并取得了良好的效果。这些数据表明,在标准的一线和二线疗法失败后,作为三线疗法使用的阿扎胞苷可产生异常持久的阳性血液学反应。此外,患者的生活质量很高,没有出现与全血细胞减少症相关的并发症,在本报告撰写期间,患者的生活质量依然很高。
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Long-term hematologic response after azacitidine treatment in a lower-risk myelodysplastic syndrome patient: A case report

We report results of a 65-year-old patient with lower-risk myelodysplastic syndrome and multilineage dysplasia treated with hypomethylating agents. After failure of erythropoietin and thalidomide, the patient received azacitidine and achieved hematological remission for 95 months. In 2016, the treatment was switched to decitabine with promising results. These data showed that azacitidine used as a third-line treatment resulted in an exceptionally long-lasting positive hematological response after standard first- and second-line therapies had failed. Additionally, the patient experienced a good quality of life with no complications related to profound cytopenia, and continues to do so at the time of this report's preparation.

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来源期刊
Leukemia Research Reports
Leukemia Research Reports Medicine-Oncology
CiteScore
1.70
自引率
0.00%
发文量
70
审稿时长
23 weeks
期刊最新文献
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