Department of Leukemia, The University of Texas MD Anderson Cancer Center , Houston, TX, USA.
Expert Opin Emerg Drugs. 2020 Dec;25(4):515-529. doi: 10.1080/14728214.2020.1854224. Epub 2020 Dec 13.
: Chronic myelomonocytic leukemia (CMML) is a clonal hematologic disorder with heterogenous prognosis, but with no curative therapies with exception of allogeneic transplant. Therapeutic options for patients with CMML are limited, and although hypomethylating agents such as azacitidine and decitabine are the standard of care, only 40% of patients achieve a response, and most responses are transient. Over the last 5 years, significant advances have been made in the understanding of the clonal landscape of CMML, some of the mechanisms associated to resistance to HMA, and other key biological processes involved in disease pathogenesis. : The current article reviews the most relevant emerging therapies currently undergoing clinical trials for the treatment of previously untreated or relapsed CMML. : The presence of recurrent somatic mutations in CMML represents therapeutic opportunities to utilize specific small molecule inhibitors such as IDH, FLT3, MEK/ERK, PLK1, or splicing inhibitors and modulators. In addition, other novel agents such as immune therapies, BCL2 or MCL1 inhibitors and other monoclonal antibodies could lead to therapeutic advances. Identifying specific patient populations likely to benefit from some of these interventions, and development of optimal combinations will remain the challenge when determining their role in therapy.
慢性髓单核细胞白血病(CMML)是一种具有异质性预后的克隆性血液病,但除异基因移植外,尚无治愈方法。CMML 患者的治疗选择有限,虽然低甲基化剂如阿扎胞苷和地西他滨是标准治疗方法,但只有 40%的患者有反应,而且大多数反应是短暂的。在过去的 5 年中,人们对 CMML 的克隆景观、与 HMA 耐药相关的一些机制以及疾病发病机制中涉及的其他关键生物学过程有了更深入的了解。本文综述了目前正在进行临床试验的用于治疗初治或复发 CMML 的最相关新兴疗法。CMML 中存在复发性体细胞突变,为利用特定的小分子抑制剂(如 IDH、FLT3、MEK/ERK、PLK1 或剪接抑制剂和调节剂)提供了治疗机会。此外,其他新型药物,如免疫疗法、BCL2 或 MCL1 抑制剂和其他单克隆抗体,可能会带来治疗进展。确定可能从这些干预措施中获益的特定患者人群,并确定最佳组合,这将是在确定其在治疗中的作用时面临的挑战。