同种异体造血干细胞移植治疗带有种系 DDX41 基因突变的急性髓性白血病

IF 0.7 Q4 HEMATOLOGY Case Reports in Hematology Pub Date : 2024-11-01 eCollection Date: 2024-01-01 DOI:10.1155/2024/4611649
Shuro Yoshida, Yuichiro Semba, Shuichiro Takashima, Masanori Kadowaki, Ken Takase, Takahiro Maeda, Koichi Akashi, Hiromi Iwasaki
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引用次数: 0

摘要

根据2016年世界卫生组织的分类,种系DEAD-box螺旋酶41基因(DDX41)突变的髓系肿瘤被新分类。种系DDX41基因突变的急性髓性白血病(AML)的临床过程尚未明确。早期病情进展缓慢,缓解率高,预后良好。另一方面,在晚期,逐渐复发率增加,最终预后可能很差。目前,关于种系 DDX41 基因突变的急性髓细胞性白血病异基因造血干细胞移植(异基因造血干细胞移植)的适应症尚未有明确的指导意见。然而,我们认为,参照之前的相关论文,对于符合异基因造血干细胞移植条件的种系DDX41突变急性髓细胞性白血病患者,应进行异基因造血干细胞移植,以克服无复发生存率低的问题。我们报告了一名 49 岁的患者,他患有泛发性血小板减少症,最终被诊断为种系 DDX41 基因突变和急性髓细胞白血病。我们决定进行异基因造血干细胞移植。第 68 天,他并发了急性移植物抗宿主病(肠道 1 期 II 级),开始使用泼尼松龙 0.2 mg/kg。他很快康复,目前已存活近两年,没有出现移植物抗宿主病的症状。关于为具有种系 DDX41 基因突变的急性髓细胞性白血病患者进行异基因造血干细胞移植的供体搜索,如果供体为家族供体,则必须确保供体的该基因突变为阴性。如果亲属捐献者的基因突变呈阳性,可能导致捐献者衍生白血病的发生,那么异基因造血干细胞移植应由非亲属捐献者进行。
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Allogeneic Hematopoietic Stem Cell Transplantation for Acute Myeloid Leukemia With a Germline DDX41 Mutation.

According to the 2016 World Health Organization classification, a germline DEAD-box helicase 41 gene (DDX41) mutation with myeloid neoplasms has been newly classified. The clinical course of acute myeloid leukemia (AML) with a germline DDX41 mutation has not yet been clarified. In the early phase, this condition is slowly progressive, the rate of remission induction is high, and the prognosis is good. On the other hand, in the late phase, the gradual relapse rate increases and the ultimate prognosis can be poor. Currently, clear guidance on the indication for allogeneic hematopoietic stem cell transplantation (allogeneic HSCT) for AML with a germline DDX41 mutation has not been yet provided. However, we consider that allogeneic HSCT should be performed in patients who are eligible for allogeneic HSCT for germline DDX41 mutations in AML to overcome poor relapse-free survival, referring to previous relevant papers. We report a 49-year-old patient who had pancytopenia and was finally diagnosed with a germline DDX41 mutation and AML. We decided to perform allogeneic HSCT. On day 68, he was complicated by acute graft versus host disease, gut stage 1, grade II, and was started on prednisolone 0.2 mg/kg. He recovered quickly and has been currently alive without symptoms of graft versus host disease for almost 2 years. Regarding donor search for allogeneic HSCT for AML with a germline DDX41 mutation, it is essential to ensure that the donor must be negative for this mutation when the donor is a family donor. If the related donor has a positive mutation, which can cause the development of donor-derived leukemia, allogeneic HSCT should performed from an unrelated donor.

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