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急性髓系白血病

Acute myeloid leukaemia.

作者信息

Estey Elihu, Döhner Hartmut

机构信息

Leukemia Department, University of Texas M D Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

Lancet. 2006 Nov 25;368(9550):1894-907. doi: 10.1016/S0140-6736(06)69780-8.


DOI:10.1016/S0140-6736(06)69780-8
PMID:17126723
Abstract

Acute myeloid leukaemia (AML) is a heterogeneous clonal disorder of haemopoietic progenitor cells and the most common malignant myeloid disorder in adults. The median age at presentation for patients with AML is 70 years. In the past few years, research in molecular biology has been instrumental in deciphering the pathogenesis of the disease. Genetic defects are thought to be the most important factors in determining the response to chemotherapy and outcome. Whereas significant progress has been made in the treatment of younger adults, the prospects for elderly patients have remained dismal, with median survival times of only a few months. This difference is related to comorbidities associated with ageing and to disease biology. Current efforts in clinical research focus on the assessment of targeted therapies. Such new approaches will probably lead to an increase in the cure rate.

摘要

急性髓系白血病(AML)是造血祖细胞的一种异质性克隆性疾病,也是成人中最常见的恶性髓系疾病。AML患者的中位发病年龄为70岁。在过去几年中,分子生物学研究有助于阐明该疾病的发病机制。基因缺陷被认为是决定化疗反应和预后的最重要因素。虽然在年轻成人的治疗方面取得了显著进展,但老年患者的前景依然黯淡,中位生存时间仅为几个月。这种差异与衰老相关的合并症以及疾病生物学有关。目前临床研究的努力集中在评估靶向治疗。这些新方法可能会提高治愈率。

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