Section of Hematology/Oncology, University of Chicago, Chicago, IL 60637, USA.
Leukemia Program, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH 44195, USA.
Blood Rev. 2021 Jul;48:100791. doi: 10.1016/j.blre.2020.100791. Epub 2020 Dec 27.
Myelodysplastic syndromes (MDS) are characterized by ineffective hematopoiesis with varying degrees of dysplasia and peripheral cytopenias. MDS are driven by structural chromosomal alterations and somatic mutations in neoplastic myeloid cells, which are supported by a tumorigenic and a proinflammatory marrow microenvironment. Current treatment strategies for lower-risk MDS focus on improving quality of life and cytopenias, while prolonging survival and delaying disease progression is the focus for higher-risk MDS. Several promising drugs are in the horizon, including the hypoxia-inducible factor stabilizer roxadustat, telomerase inhibitor imetelstat, oral hypomethylating agents (CC-486), TP53 modulators (APR-246 and ALRN-6924), and the anti-CD47 antibody magrolimab. Targeted therapies approved for acute myeloid leukemia treatment, such as isocitrate dehdyrogenase inhibitors and venetoclax, are also being studied for use in MDS. In this review, we provide a brief overview of pathogenesis and current treatment strategies in MDS followed by a discussion of newer agents that are under clinical investigation.
骨髓增生异常综合征(MDS)的特征是无效造血,伴有不同程度的发育异常和外周血细胞减少。MDS 由肿瘤性髓系细胞的结构染色体改变和体细胞突变驱动,这得到了致瘤性和促炎骨髓微环境的支持。目前针对低危 MDS 的治疗策略侧重于改善生活质量和血细胞减少症,而延长生存时间和延缓疾病进展则是高危 MDS 的重点。一些有前途的药物正在研发中,包括缺氧诱导因子稳定剂罗沙司他、端粒酶抑制剂imetelstat、口服低甲基化剂(CC-486)、TP53 调节剂(APR-246 和 ALRN-6924)和抗 CD47 抗体 magrolimab。已批准用于急性髓系白血病治疗的靶向药物,如异柠檬酸脱氢酶抑制剂和 venetoclax,也正在研究用于 MDS 的治疗。在这篇综述中,我们简要概述了 MDS 的发病机制和当前的治疗策略,随后讨论了正在临床研究中的新型药物。