急性早幼粒细胞白血病
癌症研究
医学
干细胞
遗传增强
造血干细胞移植
造血
融合基因
移植
维甲酸
白血病
化疗
维甲酸
造血干细胞
免疫学
肿瘤科
基因
内科学
生物
遗传学
作者
Li Chen,Hongming Zhu,Yongmei Zhu,Jin Wen,Fangyi Dong,Jianfeng Li,Jiong Hu,Qiusheng Chen,Kankan Wang,Junmin Li
标识
DOI:10.3389/fonc.2022.1013046
摘要
Acute promyelocytic leukemia (APL) is characterized by the balanced translocation of chromosomes 15 and 17, resulting in the formation of PML-RARA fusion gene. More than 98% of APL have PML-RARA fusion, and less than 2% have other types of RARA gene partners, which named variant APL (vAPL). In the present study, we reported a vAPL with BCOR-RARA, which was the third case of BCOR-RARA APL published. The patient achieved complete remission (CR) with all-trans retinoic acid (ATRA) monotherapy, and molecular CR with ATRA plus standard chemotherapy. After that, he underwent allogeneic hematopoietic stem cell transplantation (allo-HSCT) and ATRA maintenance and maintained a molecular CR status. This case provided valuable insights into the accurate identification of vAPL. Moreover, ATRA combined with chemotherapy followed by allo-HSCT was suggested as an optimal choice for those vAPL patients who had a high risk of relapse.
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