SOHO State of the Art Updates and Next Questions: IDH Inhibition

被引:0
|
作者
Dragani, Matteo [1 ]
de Botton, Stephane [1 ]
机构
[1] Gustave Roussy Canc Ctr, Dept Hematol, 114 Rue Edouard Vaillant, F-94805 Villejuif, France
来源
CLINICAL LYMPHOMA MYELOMA & LEUKEMIA | 2021年 / 21卷 / 09期
关键词
AML; Enasidenib; Ivosidenib; MDS; Targeted therapy; ACUTE MYELOID-LEUKEMIA; ISOCITRATE DEHYDROGENASE MUTATIONS; PROGNOSTIC-SIGNIFICANCE; MYELODYSPLASTIC SYNDROMES; ENZYME ISOFORMS; RETINOIC ACID; ASSOCIATION; IVOSIDENIB; ENASIDENIB; DEPENDS;
D O I
10.1016/j.clml.2021.05.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
There has been extraordinary progress in the field of targeted therapy for myeloid malignancies in the last few years, especially due to the approval of various agents that can be used as monotherapy or in combination as first-line treatment or when facing a refractory or relapsed disease. Many successful trials have been conducted recently, and a consistent body of work about the efficacy of novel molecules is now available. In this review, we sought to explain how enasidenib and ivosidenib have changed the face of myeloid neoplasm treatment through isocitrate dehydrogenase inhibition and to summarize the trials results that have led to the current commercial indications for the two molecules. (C) 2021 Published by Elsevier Inc.
引用
收藏
页码:567 / 572
页数:6
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