TP53突变髓系肿瘤的非移植治疗方法。

IF 2.9 3区 教育学 Q1 EDUCATION, SCIENTIFIC DISCIPLINES
Ansh K Mehta, Marina Konopleva
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引用次数: 0

摘要

tp53突变的骨髓增生异常综合征(MDS)和急性髓系白血病(AML)仍然是一种具有挑战性的预后不良的克隆性髓系疾病。最近的研究表明,在双等位基因TP53缺失的AML、MDS和MDS/AML中,TP53突变的克隆成为显性克隆。这些都是高度侵袭性的疾病,对大多数化疗都有抗药性。最新的2022年国际共识分类将这些疾病归类为“TP53突变的髓系疾病”。并不是所有的治疗方法都能提高这种疾病的生存率。许多新的治疗方法即将出现,包括嵌合抗原受体T/ nk细胞疗法、突变p53再激活剂、Fc融合蛋白和针对各种髓系抗原的单克隆抗体。本文综述了目前治疗髓系疾病TP53突变的方法,并概述了新兴的非移植方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nontransplant treatment approaches for myeloid neoplasm with mutated TP53.

TP53-mutated myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML) remain a challenging spectrum of clonal myeloid disease with poor prognosis. Recent studies have shown that in AML, MDS, and MDS/AML with biallelic TP53 loss, the TP53-mutated clone becomes dominant. These are highly aggressive diseases that are resistant to most chemotherapies. The latest 2022 International Consensus Classification categorizes these diseases under "myeloid disease with mutated TP53." All treatment approaches have not improved survival rates for this disease. Many newer therapies are on the horizon, including chimeric antigen receptor T/NK-cell therapies, mutated p53 reactivators, Fc fusion protein, and monoclonal antibodies targeting various myeloid antigens. This review summarizes the current approaches for myeloid disease with TP53 mutation and provides an overview of emerging nontransplant approaches.

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来源期刊
Hematology. American Society of Hematology. Education Program
Hematology. American Society of Hematology. Education Program EDUCATION, SCIENTIFIC DISCIPLINES-HEMATOLOGY
CiteScore
4.70
自引率
3.30%
发文量
0
期刊介绍: Hematology, the ASH Education Program, is published annually by the American Society of Hematology (ASH) in one volume per year.
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