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整合照护低危骨髓增生异常综合征患者。

Integrating care for patients with lower risk myelodysplastic syndrome.

机构信息

Department of Leukemia, University of Texas M.D. Anderson Cancer Center, Houston, USA.

出版信息

Semin Oncol. 2011 Oct;38(5):658-66. doi: 10.1053/j.seminoncol.2011.06.002.

Abstract

Patients with lower risk myelodysplastic syndrome (MDS) are those with low or intermediate-1 (INT-1) risk disease by the International Prognostic Scoring System (IPSS) index. Traditionally this has been a subset of patients where the philosophy of therapy has focused on improving transfusion needs. This is the result of the perception that the natural course of patients with lower risk disease is benign and the correct assumption that forms of therapy associated with early induction mortality cannot be justified. Over the last 5 years, we have witnessed significant improvements in our understanding of the natural history and therapy of patients with lower risk MDS. That said, it is not clear that any of these approaches improves survival. In this chapter, I will try to integrate information provided in other articles presented in this issue of Seminars in Oncology with new information regarding the heterogeneity of the natural history of patients with lower risk MDS and propose a framework for future research initiatives for this group of patients.

摘要

低危骨髓增生异常综合征(MDS)患者是国际预后评分系统(IPSS)指数低危或中危-1(INT-1)的患者。传统上,这是一组以治疗理念为重点改善输血需求的患者。这是因为人们认为低危疾病患者的自然病程是良性的,并且正确地假设与早期诱导死亡率相关的治疗形式是不合理的。在过去的 5 年中,我们对低危 MDS 患者的自然史和治疗有了更深入的了解。也就是说,目前尚不清楚这些方法中的任何一种是否能提高生存率。在这一章中,我将尝试整合本专题中的其他文章提供的信息,并结合有关低危 MDS 患者自然史异质性的新信息,为这组患者的未来研究计划提出一个框架。

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