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老年患者的急性髓系白血病和骨髓增生异常综合征

Acute myeloid leukemia and myelodysplastic syndromes in older patients.

作者信息

Estey Elihu

机构信息

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

出版信息

J Clin Oncol. 2007 May 10;25(14):1908-15. doi: 10.1200/JCO.2006.10.2731.

DOI:10.1200/JCO.2006.10.2731
PMID:17488990
Abstract

The median age of patients with acute myeloid leukemia (AML) is 65 to 70 years. The majority of older patients with AML probably do not receive specific treatment, and those who receive standard regimens have a median survival time of less than 1 year. This suggests that, in general, older patients should receive investigational therapy; however, factors other than age influence survival after administration of standard treatment and need to be accounted for when making treatment recommendations. In some cases where investigational therapy is unavailable, palliative care may be the best option. Like AML, myelodysplastic syndrome (MDS) is a disease of the elderly. It is divided into higher and lower risk groups. The natural history of high-risk MDS (eg, > 10% marrow blasts) bears more resemblance to that of AML than to that of an indolent disorder; accordingly, similar therapeutic considerations apply. The more benign natural history of lower risk MDS leads to consideration of reduction in transfusion needs and improvement in quality of life as primary goals of therapy. Lenalidomide, azacitidine, and decitabine, each recently approved by the US Food and Drug Administration, are useful in achieving these objectives.

摘要

急性髓系白血病(AML)患者的中位年龄为65至70岁。大多数老年AML患者可能未接受特异性治疗,而接受标准方案治疗的患者中位生存时间不到1年。这表明,一般而言,老年患者应接受试验性治疗;然而,除年龄外,其他因素也会影响标准治疗后的生存情况,在提出治疗建议时需要加以考虑。在某些无法获得试验性治疗的情况下,姑息治疗可能是最佳选择。与AML一样,骨髓增生异常综合征(MDS)也是一种老年疾病。它分为高危和低危组。高危MDS(如骨髓原始细胞>10%)的自然病程与AML的更为相似,而与惰性疾病的不同;因此,适用类似的治疗考量。低危MDS更为良性的自然病程使得将减少输血需求和改善生活质量作为治疗的主要目标加以考虑。来那度胺、阿扎胞苷和地西他滨均于近期获美国食品药品监督管理局批准,对实现这些目标很有用。

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