[Two cases of systemic mastocytosis with RUNX1-RUNX1T1 positive acute myeloid leukemia treated with sequential avapritinib after allogeneic hematopoietic stem cell transplantation and literature review].

J Wang, Y L Zu, R R Gui, Z Li, Yanli Zhang, J Zhou
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引用次数: 0

Abstract

Systemic mastocytosis (SM) with RUNX1-RUNX1T1 positive acute myeloid leukemia (AML) is a rare myeloid tumor with no standard treatment. Two cases of SM patients with RUNX1-RUNX1T1 positive AML treated with sequential avapritinib after allogeneic hematopoietic stem cell transplantation (allo-HSCT) were reported in Henan Cancer Hospital. Mast cell in bone marrow disappeared, C-KIT mutation and RUNX1-RUNX1T1 fusion gene remained negative. Allo-HSCT sequential avapritinib is an effective treatment for SM patients with RUNX1-RUNX1T1 positive AML.

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[两例伴有 RUNX1-RUNX1T1 阳性急性髓性白血病的系统性肥大细胞增多症患者在异基因造血干细胞移植后连续接受阿伐替尼治疗及文献综述]。
系统性肥大细胞增多症(SM)伴RUNX1-RUNX1T1阳性急性髓系白血病(AML)是一种罕见的髓系肿瘤,目前尚无标准治疗方法。河南省肿瘤医院报道了两例RUNX1-RUNX1T1阳性急性髓细胞白血病(AML)的肥大细胞增多症患者,他们在接受异基因造血干细胞移植(allo-HSCT)后连续使用阿伐替尼治疗。骨髓中肥大细胞消失,C-KIT突变和RUNX1-RUNX1T1融合基因保持阴性。对于RUNX1-RUNX1T1阳性急性髓细胞白血病SM患者,allo-HSCT序贯阿伐替尼是一种有效的治疗方法。
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CiteScore
0.80
自引率
0.00%
发文量
100
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