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急性髓系白血病的治疗策略。

Treatment strategies in acute myeloid leukemia.

机构信息

Department of Hematology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

出版信息

Chin Med J (Engl). 2011 May;124(9):1409-21.

PMID:21740756
Abstract

OBJECTIVE

To summarize the risk stratification and current treatment strategies for acute myeloid leukemia (AML) and discuss the role of emerging novel agents that might be applied in future clinical trials.

DATA SOURCES

The data in this article were collected from PubMed database with relevant English articles published from 1991 to 2009.

STUDY SELECTION

Articles regarding the risk stratification and therapeutic options of AML, as well as the characteristics of leukemic stem cells were selected.

RESULTS

AML is a heterogeneous disease with variable clinical outcome dependent on several prognostic factors, including age, cytogenetics and molecular markers. The advances in the understanding of AML pathogenesis and development will generate potential novel agents that might improve the treatment results of standard chemotherapy.

CONCLUSION

Deeper insight into the multiple transforming events of AML may aid us in designing combinations of small molecule inhibitors based on the individual patient characteristics.

摘要

目的

总结急性髓系白血病(AML)的风险分层和当前治疗策略,并探讨可能应用于未来临床试验的新兴新型药物的作用。

资料来源

本文数据来源于 PubMed 数据库,检索了 1991 年至 2009 年发表的相关英文文献。

研究选择

选择了关于 AML 的风险分层和治疗选择以及白血病干细胞特征的文章。

结果

AML 是一种异质性疾病,其临床结果因多种预后因素而异,包括年龄、细胞遗传学和分子标志物。对 AML 发病机制和发展的深入了解将产生潜在的新型药物,可能改善标准化疗的治疗效果。

结论

深入了解 AML 的多种转化事件可能有助于我们根据个体患者特征设计基于小分子抑制剂的组合。

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Treatment strategies in acute myeloid leukemia.急性髓系白血病的治疗策略。
Chin Med J (Engl). 2011 May;124(9):1409-21.
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Remission induction, consolidation and novel agents in development for adults with acute myeloid leukaemia.成人急性髓系白血病缓解诱导、巩固和新开发的药物。
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FLT3 inhibitors for the treatment of acute myeloid leukemia.用于治疗急性髓系白血病的FLT3抑制剂
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Therapy of acute myeloid leukemia: towards a patient-oriented, risk-adapted approach.急性髓系白血病的治疗:迈向以患者为导向、风险适应性治疗方法
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Treatment of acute myeloid leukemia by directly targeting both leukemia stem cells and oncogenic molecule with specific scFv-immunolipoplexes as a deliverer.以特异性单链抗体片段免疫脂质复合体作为载体,通过直接靶向白血病干细胞和致癌分子来治疗急性髓系白血病。
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