Smilow Cancer Center at Yale New Haven Hospital, New Haven, Connecticut, USA.
Curr Opin Hematol. 2019 Mar;26(2):77-87. doi: 10.1097/MOH.0000000000000483.
Myelodysplastic syndromes (MDS) are a diverse group of clonal disorders of hematopoietic stem or progenitor cells that represent the most common class of acquired bone marrow failure syndromes in adults. Despite significant improvement in the pathologic insight into this group of disorders, therapeutic options remain limited and allogeneic hematopoietic stem-cell transplantation is the only treatment that can induce long-term remission in patients with MDS. The goals of therapy for MDS are based on disease prognostication, with a focus of minimizing transfusion dependence and preserving quality of life in low-risk groups and preventing progression of disease to acute myeloid leukemia in high-risk groups. Given the dearth of approved treatment options, there is a marked need for novel therapies across the board, and there are several novel agents currently in the pipeline.
Among the promising agents with preclinical and early phase efficacy in higher risk MDS, apoptosis targeting with BCL-2 inhibitors have been a standout. There is also a keen interest in immunotherapy, and targeted agents (genetic, signaling pathways, bispecific antibodies, antibody-drug conjugates, and others described in this review).
In this review, we will highlight some of the promising new agents currently under investigation for the management of MDS.
骨髓增生异常综合征(MDS)是一组异质性造血干/祖细胞克隆性疾病,是成人获得性骨髓衰竭综合征中最常见的一类。尽管对这类疾病的病理认识有了显著提高,但治疗选择仍然有限,异基因造血干细胞移植是唯一能诱导 MDS 患者长期缓解的治疗方法。MDS 的治疗目标基于疾病预后,重点是减少低危组患者的输血依赖,维持生活质量,并防止高危组疾病进展为急性髓系白血病。鉴于批准的治疗方案匮乏,全面需要新的治疗方法,目前有几种新型药物正在研发中。
在高危 MDS 中具有临床前和早期疗效的有前途的药物中,靶向凋亡的 BCL-2 抑制剂引人注目。免疫疗法也受到了极大的关注,靶向药物(遗传、信号通路、双特异性抗体、抗体药物偶联物等,在本文中都有描述)。
在这篇综述中,我们将重点介绍一些目前正在研究用于 MDS 治疗的有前途的新型药物。