Venetoclax 治疗 TNRC18::RARA 融合基因的 ATRA 和 ATO 抗性急性早幼粒细胞白血病患者

IF 0.7 Q4 HEMATOLOGY
Weina Li , Haijie Li , Xueyan Chen , Yan Zheng
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引用次数: 0

摘要

变异型急性早幼粒细胞白血病(APL)给诊断和治疗带来了挑战,主要原因是缺乏 PML::RARA。本报告介绍了一例被诊断为携带 TNRC18::RARA 融合基因的全反式维甲酸(ATRA)耐药 APL 患者的病例。在接受venetoclax、阿扎胞苷和ATRA治疗后,患者获得了完全缓解。该患者还患上了肺结核和耐多药感染,在分别接受抗结核治疗和卡林霉素治疗后,病情有了很大改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Venetoclax for an ATRA and ATO resistance acute promyelocytic leukemia patient with TNRC18::RARA fusion gene
Variant acute promyelocytic leukemia (APL) poses diagnostic and therapeutic challenges primarily because of the absence of PML::RARA. This report presents the case of a patient diagnosed with all-trans retinoic acid (ATRA)-resistant APL harboring the TNRC18::RARA fusion gene. After treatment with venetoclax, azacitidine, and ATRA, the patient achieved complete remission. The patient also developed pulmonary tuberculosis and a multidrug-resistant infection, which improved considerably after antituberculosis treatment and carrimycin, respectively.
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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
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