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我如何治疗急性髓系白血病。

How I treat acute myeloid leukemia.

机构信息

Rambam Health Care Campus and Technion, Israel Institute of Technology, Haifa, Israel.

出版信息

Blood. 2010 Oct 28;116(17):3147-56. doi: 10.1182/blood-2010-05-260117. Epub 2010 Jun 17.

Abstract

More than one quarter of a million adults throughout the world are diagnosed annually with acute myeloid leukemia (AML). Despite considerable progress during the past 3 decades in the therapy of AML, two-thirds of young adults and 90% of older adults still die of their disease. The reported median age has increased over the past few decades, mostly because of a greater willingness of physicians to diagnose and treat older patients, and now is 72 years. The greatest challenge is in this age group. However, much improvement in therapy is needed for all adults with AML. Recent advances in allogeneic transplantation, a better understanding of prognostic factors, and development of targeted agents have only modestly improved overall outcome when large populations of patients are considered. Although an explosion in knowledge about the molecular pathogenesis of AML has outpaced treatment advances, such insights hold promise for the development of new therapies directed at specific molecular abnormalities that perturb malignant cell survival pathways. The current approach in 2010 to the management of this disease is presented through a discussion of illustrative cases.

摘要

全世界每年有超过 25 万成年人被诊断患有急性髓细胞白血病(AML)。尽管在过去 30 年中,AML 的治疗取得了相当大的进展,但三分之二的年轻成年人和 90%的老年成年人仍死于该病。过去几十年中,报告的中位年龄有所增加,这主要是因为医生更愿意诊断和治疗老年患者,现在的年龄为 72 岁。最大的挑战是在这个年龄段。然而,所有 AML 成年患者都需要在治疗方面取得更大的进展。异基因移植的最新进展、对预后因素的更好理解以及靶向药物的开发,仅当考虑到大量患者时,才会适度改善总体预后。尽管关于 AML 分子发病机制的知识呈爆炸式增长,但治疗进展却落后于这种情况,这些观点为开发针对扰乱恶性细胞存活途径的特定分子异常的新疗法提供了希望。通过讨论说明性病例,介绍了 2010 年这种疾病的管理方法。

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