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靶向不可成药靶点:Menin 抑制剂呼之欲出。

Targeting the undruggable: menin inhibitors ante portas.

机构信息

University of Munich, Campus Grosshadern, Medical Clinic III, Marchioninistrasse 15, 81377, Munich, Germany.

Haematology and Oncology, Carl Thiem Clinic, Cottbus, Germany.

出版信息

J Cancer Res Clin Oncol. 2023 Sep;149(11):9451-9459. doi: 10.1007/s00432-023-04752-9. Epub 2023 Apr 27.

Abstract

Acute myeloid leukaemias harbouring a rearrangement of the mixed lineage leukaemia gene (MLL) are aggressive haematopoietic malignancies that relapse early and have a poor prognosis (event-free survival less than 50%). Menin is a tumour suppressor, however, in MLL-rearranged leukaemias it functions as a co-factor which is mandatory for the leukaemic transformation by interaction with the N-terminal part of MLL, which is maintained in all MLL-fusion proteins. Inhibition of menin blocks leukaemogenesis and leads to differentiation and, in turn, to apoptosis of leukaemic blasts. Furthermore, nucleophosmin 1 (NPM1) binds to specific chromatin targets, which are co-occupied by MLL, and menin inhibition has been shown to trigger degradation of mNPM1 resulting in a rapid decrease in gene expression and activating histone modifications. Therefore, disruption of the menin-MLL axis blocks leukaemias driven by NPM1 mutations for which the expression of menin-MLL target genes (e.g., MEIS1, HOX etc.) is essential. To date at least six different menin-MLL inhibitors are undergoing clinical evaluation as first- and second-line monotherapy in acute leukaemias: DS-1594, BMF-219, JNJ-75276617, DSP-5336, revumenib, and ziftomenib, however, only for revumenib and ziftomenib early clinical data have been reported. In the revumenib phase I/II AUGMENT-101 trial (N = 68) with very heavily pretreated AML patients the ORR was 53% with a CR rate of 20%. The ORR in patients harbouring MLL rearrangement of mNPM1 was 59%. Patients who achieved a response had a mOS of 7 months. Similar results have been reported for ziftomenib in the phase I/II COMET-001 trial. ORR was 40% and CRc was 35% in AML patients with mNPM1. However, outcome was worse in AML patients with a MLL rearrangement (ORR 16.7%, CRc 11%). Differentiation syndrome was a notable adverse event. The clinical development of novel menin-MLL inhibitors is well in line with the currently ongoing paradigm shift towards targeted therapies seen in the AML treatment landscape. Moreover, the clinical assessment of combinations of these inhibitors with established therapy options in AML could be the fuel for an improved outcome of MLL/NPM1 patients.

摘要

急性髓系白血病(AML)伴混合谱系白血病(MLL)基因重排是一种侵袭性血液系统恶性肿瘤,其早期复发且预后不良(无事件生存<50%)。Menin 是一种肿瘤抑制因子,但在 MLL 重排的白血病中,它作为一种辅助因子发挥作用,通过与 MLL 的 N 端部分相互作用,对于白血病转化是必需的,而所有 MLL 融合蛋白都保留了 MLL 的 N 端部分。抑制 Menin 可阻断白血病的发生,并导致白血病母细胞的分化和凋亡。此外,核磷蛋白 1(NPM1)与特定染色质靶标结合,而 MLL 与这些靶标共同占据,抑制 Menin 已被证明可触发 mNPM1 的降解,从而导致基因表达的迅速下降,并激活组蛋白修饰。因此,破坏 Menin-MLL 轴可阻断由 NPM1 突变驱动的白血病,而 Menin-MLL 靶基因(如 MEIS1、HOX 等)的表达对于这些白血病至关重要。迄今为止,至少有六种不同的 Menin-MLL 抑制剂正在作为急性白血病的一线和二线单药进行临床评估:DS-1594、BMF-219、JNJ-75276617、DSP-5336、revumenib 和 ziftomenib,但仅针对 revumenib 和 ziftomenib 有早期临床数据报告。在 revumenib 的 I/II 期 AUGMENT-101 试验(N=68)中,对非常预处理过的 AML 患者进行治疗,ORR 为 53%,完全缓解率(CR)为 20%。在携带 mNPM1 的 MLL 重排的患者中,ORR 为 59%。获得缓解的患者的中位总生存期(mOS)为 7 个月。在 I/II 期 COMET-001 试验中,ziftomenib 也报告了类似的结果。在携带 mNPM1 的 AML 患者中,ORR 为 40%,CRc 为 35%。然而,在 MLL 重排的 AML 患者中,结局更差(ORR 16.7%,CRc 11%)。分化综合征是一个显著的不良事件。新型 Menin-MLL 抑制剂的临床开发与 AML 治疗领域目前正在进行的靶向治疗范式转变非常一致。此外,在 AML 中评估这些抑制剂与现有治疗方案的联合应用,可能为改善 MLL/NPM1 患者的预后提供动力。

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