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细胞周期抑制剂治疗急性髓细胞白血病的研究进展:Ⅱ期和Ⅲ期临床试验综述。

Cell cycle inhibitors for the treatment of acute myeloid leukemia: a review of phase 2 & 3 clinical trials.

机构信息

Department of Leukemia, University of Texas, MD Anderson Cancer Center , Houston, Texas, USA.

出版信息

Expert Opin Emerg Drugs. 2020 Dec;25(4):491-499. doi: 10.1080/14728214.2020.1847272. Epub 2020 Nov 19.

Abstract

: Acute myeloid leukemia (AML) is a clinically heterogeneous hematologic malignancy with poor long term outcomes. Cytotoxic chemotherapy remains the backbone of therapy especially among younger patients; however the effective incorporation of targeted therapies continues to be an area of active research in an effort to improve response durations and survival. Cell cycle inhibitors (CCI) are a novel class of agents which may be of particular interest for development in patients with AML. : We will review the concept of CCIs along with available pre-clinical and clinical data in the treatment of AML both in North America and abroad. Specific drug targets reviewed include cyclin D kinase, Aurora kinase, CHK1, and WEE1. : Utilization of CCIs in patients with AML is an emerging approach that has shown promise in pre-clinical models. It has been challenging to translate this concept into clinical success thus far, due to marginal single-agent activity and significant toxicity profiles, however clinical evaluation is ongoing. Addition of these agents to cytotoxic chemotherapy and other targeted therapies provides a potential combinatorial path forward for this novel class of therapies. Developing optimal combinations while balancing toxicity are among the top clinical challenges that must be overcome before we can anticipate adoption of these agents into the armamentarium of AML therapy.

摘要

急性髓系白血病 (AML) 是一种临床异质性血液恶性肿瘤,长期预后较差。细胞毒性化疗仍然是治疗的基础,特别是在年轻患者中;然而,为了提高反应持续时间和生存率,靶向治疗的有效纳入仍然是一个积极研究的领域。细胞周期抑制剂 (CCI) 是一类新型药物,对于 AML 患者的开发可能具有特别的意义。

我们将回顾 CCIs 的概念,以及在北美和国外 AML 治疗中的可用临床前和临床数据。回顾的具体药物靶点包括周期蛋白依赖性激酶、极光激酶、CHK1 和 WEE1。

在 AML 患者中使用 CCIs 是一种新兴的方法,在临床前模型中显示出了希望。迄今为止,由于单一药物活性差和毒性谱显著,将这一概念转化为临床成功一直具有挑战性,但临床评估仍在进行中。将这些药物与细胞毒性化疗和其他靶向治疗联合使用,为这一新类药物提供了一种潜在的组合治疗途径。在我们能够期望将这些药物纳入 AML 治疗方案之前,需要克服开发最佳组合同时平衡毒性的最高临床挑战。

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