Oran Betul
Department of Stem Cell Transplantation and Cellular Therapy, University of Texas MD Anderson Cancer Center, Houston, TX.
Clin Lymphoma Myeloma Leuk. 2015 Jun;15 Suppl:S43-9. doi: 10.1016/j.clml.2015.04.002.
Allogeneic hematopoietic stem cell transplantation (SCT) can cure a proportion of patients with myelodysplastic syndromes (MDS). However, treatment related toxicities, graft versus host disease, infectious complications and relapse remain major problems post transplant. Further, recent new developments with innovative drugs including hypomethylating agents (HMA) have extended the therapeutic alternatives for our patients. Nevertheless, with the introduction of reduced-intensity conditioning and thereby reducing early mortality, transplant numbers in MDS patients have significantly increased recently. In the absence of prospective randomized trials emphasis should be put on patient selection and optimization of the pre- and post-transplant treatment in order to achieve long-term disease control and at the same time maintain an adequate quality of life. With better understanding of disease biology and prognosis and with different types of conditioning regimens as well as different graft sources, a transplant strategy should be tailored to the individual host to maximize the benefits of this procedure.
异基因造血干细胞移植(SCT)可治愈一部分骨髓增生异常综合征(MDS)患者。然而,治疗相关毒性、移植物抗宿主病、感染并发症和复发仍是移植后的主要问题。此外,包括低甲基化药物(HMA)在内的创新药物的最新进展为我们的患者扩展了治疗选择。尽管如此,随着减低强度预处理的引入从而降低了早期死亡率,MDS患者的移植数量最近显著增加。在缺乏前瞻性随机试验的情况下,应着重于患者选择以及移植前后治疗的优化,以实现长期疾病控制,同时维持适当的生活质量。随着对疾病生物学和预后的更好理解,以及不同类型的预处理方案和不同的移植物来源,应根据个体宿主量身定制移植策略,以最大化该治疗手段的益处。