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Enasidenib-induced differentiation promotes sensitivity to venetoclax in IDH2-mutated acute myeloid leukemia.

作者信息

Cathelin Severine, Sharon David, Subedi Amit, Cojocari Dan, Phillips Darren C, Leverson Joel D, MacBeth Kyle J, Nicolay Brandon, Narayanaswamy Rohini, Ronseaux Sebastien, Liu Guowen, Chan Steven M

机构信息

Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.

Oncology Discovery, AbbVie Inc., North Chicago, IL, USA.

出版信息

Leukemia. 2022 Mar;36(3):869-872. doi: 10.1038/s41375-021-01468-y. Epub 2021 Nov 6.

DOI:10.1038/s41375-021-01468-y
PMID:34743189
Abstract
摘要

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Enasidenib-induced differentiation promotes sensitivity to venetoclax in IDH2-mutated acute myeloid leukemia.艾伏尼布诱导的分化增强了异柠檬酸脱氢酶2(IDH2)突变的急性髓系白血病对维奈克拉的敏感性。
Leukemia. 2022 Mar;36(3):869-872. doi: 10.1038/s41375-021-01468-y. Epub 2021 Nov 6.
2
A pharmacogenomic approach validates AG-221 as an effective and on-target therapy in IDH2 mutant AML.一种药物基因组学方法验证了AG-221作为异柠檬酸脱氢酶2(IDH2)突变的急性髓系白血病(AML)的有效且靶向治疗药物。
Leukemia. 2017 Jun;31(6):1466-1470. doi: 10.1038/leu.2017.84. Epub 2017 Mar 10.
3
Midostaurin, enasidenib, CPX-351, gemtuzumab ozogamicin, and venetoclax bring new hope to AML.米哚妥林、恩西地平、CPX-351、奥加曲珠单抗和维奈托克为 AML 带来新希望。
Blood. 2017 Dec 7;130(23):2469-2474. doi: 10.1182/blood-2017-08-784066. Epub 2017 Oct 19.
4
Enasidenib for patients with relapsed acute myeloid leukemia and the IDH2 mutation.恩杂鲁胺用于复发急性髓系白血病伴异柠檬酸脱氢酶2(IDH2)突变的患者。
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Enasidenib in mutant relapsed or refractory acute myeloid leukemia.恩杂鲁胺用于治疗突变型复发或难治性急性髓系白血病。 (注:原文中药物名可能有误,推测正确药物名应该是Enasidenib为恩杂鲁胺,而这里治疗白血病的应该是Enasentinib,中文名为恩西地平 ,以下按照正确药物名给出译文) 恩西地平用于治疗突变型复发或难治性急性髓系白血病。
Blood. 2017 Aug 10;130(6):722-731. doi: 10.1182/blood-2017-04-779405. Epub 2017 Jun 6.
6
All-Trans Retinoic Acid Synergizes with Enasidenib to Induce Differentiation of IDH2-Mutant Acute Myeloid Leukemia Cells.全反式维甲酸与恩西地平联合诱导 IDH2 突变型急性髓系白血病细胞分化。
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Enasidenib: First Mutant IDH2 Inhibitor for the Treatment of Refractory and Relapsed Acute Myeloid Leukemia.恩杂鲁胺:首个用于治疗难治性和复发性急性髓系白血病的突变型异柠檬酸脱氢酶2抑制剂。
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Comparison of venetoclax and ivosidenib/enasidenib for unfit newly diagnosed patients with acute myeloid leukemia and mutation: a network meta-analysis.维奈托克与艾伏尼布/恩杂鲁胺用于不适合的新诊断急性髓系白血病伴 突变患者的比较:一项网状Meta分析。
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引用本文的文献

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Newly diagnosed acute myeloid leukemia in unfit patients: 2026 treatment algorithms.不适合接受治疗的新诊断急性髓系白血病患者:2026年治疗算法
Blood Cancer J. 2025 Aug 16;15(1):139. doi: 10.1038/s41408-025-01346-1.
2
Outcomes of Frontline Triplet Regimens With a Hypomethylating Agent, Venetoclax, and Isocitrate Dehydrogenase Inhibitor for Intensive Chemotherapy-Ineligible Patients With Isocitrate Dehydrogenase-Mutated AML.对于不符合强化化疗条件的异柠檬酸脱氢酶(IDH)突变型急性髓系白血病(AML)患者,采用去甲基化药物、维奈克拉和异柠檬酸脱氢酶抑制剂的一线三联方案的疗效。
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3

本文引用的文献

1
Regulation and function of Bcl-2 during differentiation-induced cell death in HL-60 promyelocytic cells.Bcl-2在HL-60早幼粒细胞分化诱导的细胞死亡过程中的调控与功能
Am J Pathol. 1995 Feb;146(2):481-90.
The prognostic significance of genetics in acute myeloid leukemia under venetoclax-based treatment.
在基于维奈克拉的治疗方案下,遗传学在急性髓系白血病中的预后意义。
Ann Hematol. 2024 Dec;103(12):5019-5033. doi: 10.1007/s00277-024-06050-x. Epub 2024 Oct 29.
4
NL101 synergizes with the BCL-2 inhibitor venetoclax through PI3K-dependent suppression of c-Myc in acute myeloid leukaemia.NL101 通过抑制 PI3K 依赖的 c-Myc 协同 BCL-2 抑制剂 venetoclax 在急性髓系白血病中发挥作用。
J Transl Med. 2024 Sep 27;22(1):867. doi: 10.1186/s12967-024-05647-0.
5
Monocytic Differentiation in Acute Myeloid Leukemia Cells: Diagnostic Criteria, Biological Heterogeneity, Mitochondrial Metabolism, Resistance to and Induction by Targeted Therapies.急性髓系白血病细胞中的单核细胞分化:诊断标准、生物学异质性、线粒体代谢、对靶向治疗的耐药性和诱导作用。
Int J Mol Sci. 2024 Jun 8;25(12):6356. doi: 10.3390/ijms25126356.
6
High Mitochondrial Protein Expression as a Potential Predictor of Relapse Risk in Acute Myeloid Leukemia Patients with the Monocytic FAB Subtypes M4 and M5.线粒体蛋白高表达作为急性髓系白血病M4和M5单核细胞FAB亚型患者复发风险的潜在预测指标
Cancers (Basel). 2023 Dec 19;16(1):8. doi: 10.3390/cancers16010008.
7
Current Advances and Future Strategies for BCL-2 Inhibitors: Potent Weapons against Cancers.BCL-2抑制剂的当前进展与未来策略:对抗癌症的有力武器
Cancers (Basel). 2023 Oct 12;15(20):4957. doi: 10.3390/cancers15204957.
8
The curious case of IDH mutant acute myeloid leukaemia: biochemistry and therapeutic approaches.IDH 突变型急性髓系白血病的奇特案例:生物化学与治疗方法。
Biochem Soc Trans. 2023 Aug 31;51(4):1675-1686. doi: 10.1042/BST20230017.
9
Characteristics and prognostic impact of IDH mutations in AML: a COG, SWOG, and ECOG analysis.IDH 突变在 AML 中的特征和预后影响:COG、SWOG 和 ECOG 分析。
Blood Adv. 2023 Oct 10;7(19):5941-5953. doi: 10.1182/bloodadvances.2022008282.
10
A Phase Ib/II Study of Ivosidenib with Venetoclax ± Azacitidine in IDH1-Mutated Myeloid Malignancies.ivosidenib 联合 venetoclax ± 阿扎胞苷治疗 IDH1 突变型髓系恶性肿瘤的 Ib/II 期研究。
Blood Cancer Discov. 2023 Jul 5;4(4):276-293. doi: 10.1158/2643-3230.BCD-22-0205.