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低危非5q缺失型骨髓增生异常综合征(MDS)治疗的最新进展。

Recent advances in the treatment of lower-risk non-del(5q) myelodysplastic syndromes (MDS).

作者信息

Almeida Antonio, Fenaux Pierre, List Alan F, Raza Azra, Platzbecker Uwe, Santini Valeria

机构信息

Instituto Português de Oncologia de Lisboa Francisco Gentil, Departamento de Hematologia, CIPM, Rua Prof. Lima Basto, 1099-023, Lisbon, Portugal.

Service d'Hématologie Séniors, Hôpital Saint-Louis, Université Paris 7, Paris, France.

出版信息

Leuk Res. 2017 Jan;52:50-57. doi: 10.1016/j.leukres.2016.11.008. Epub 2016 Nov 13.

Abstract

Patients with lower-risk myelodysplastic syndromes (MDS) are affected primarily by symptoms of chronic anemia and fatigue rather than progression to acute myeloid leukemia. Severe thrombocytopenia, although less common in lower-risk MDS, is associated with increased risk of bleeding. For anemic patients, the principal aim of treatment is to improve anemia and decrease red blood cell transfusions. For transfusion-dependent patients with lower-risk MDS without chromosome 5q deletion [non-del(5q) MDS], there are limited effective treatments. Erythropoiesis-stimulating agents (ESAs) are generally first-line therapy, yielding frequent responses with a median duration of 18-24 months. Immunosuppressive therapy or allogeneic stem cell transplantation are restricted to select patients. New strategies for ESA-refractory or relapsed patients include lenalidomide, alone or in combination with ESAs; oral azacitidine; and new molecules such as the activin receptor type II ligand traps luspatercept and sotatercept. In thrombocytopenic patients, thrombopoietin receptor agonists are under evaluation. While trials to evaluate these treatment strategies are underway, efforts are needed to optimize therapies through better patient selection and response prediction as well as integrating molecular and genetic data into clinical practice. We provide an overview of current treatment approaches for lower-risk non-del(5q) MDS and explore promising directions for future research.

摘要

低危骨髓增生异常综合征(MDS)患者主要受慢性贫血和疲劳症状影响,而非进展为急性髓系白血病。严重血小板减少症在低危MDS中虽较少见,但与出血风险增加相关。对于贫血患者,治疗的主要目标是改善贫血并减少红细胞输注。对于无5号染色体长臂缺失[非del(5q)]的低危MDS输血依赖患者,有效治疗方法有限。促红细胞生成素(ESA)通常是一线治疗,缓解率较高,中位缓解持续时间为18 - 24个月。免疫抑制治疗或异基因干细胞移植仅限于特定患者。针对ESA难治或复发患者的新策略包括来那度胺单药或与ESA联合使用、口服阿扎胞苷以及新型分子如激活素II型受体配体陷阱药物罗特西普和索特西普。对于血小板减少患者,血小板生成素受体激动剂正在评估中。虽然评估这些治疗策略的试验正在进行,但仍需通过更好的患者选择和反应预测以及将分子和遗传数据整合到临床实践中来优化治疗方法。我们概述了低危非del(5q) MDS的当前治疗方法,并探讨了未来研究的有前景方向。

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