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急性白血病的药物基因组学

Pharmacogenomics of acute leukemia.

作者信息

Cheok Meyling H, Lugthart Sanne, Evans William E

机构信息

St. Jude Children's Research Hospital, Department of Pharmaceutical Sciences, Memphis, TN 38105, USA.

出版信息

Annu Rev Pharmacol Toxicol. 2006;46:317-53. doi: 10.1146/annurev.pharmtox.45.120403.100018.

Abstract

Over the past four decades, treatment of acute leukemia in children has made remarkable progress, from this disease being lethal to now achieving cure rates of 80% for acute lymphoblastic leukemia and 45% for acute myeloid leukemia. This progress is largely owed to the optimization of existing treatment modalities rather than the discovery of new agents. However, the annual number of patients with leukemia who experience relapse after initial therapy remains greater than that of new cases of most childhood cancers. The aim of pharmacogenetics is to develop strategies to personalize medications and tailor treatment regimens to individual patients, with the goal of enhancing efficacy and safety through better understanding of the person's genetic makeup. In this review, we summarize recent pharmacogenomic studies related to the treatment of pediatric acute leukemia. These include work using candidate-gene approaches, as well as genome-wide studies using haplotype mapping and gene expression profiling. These strategies illustrate the promise of pharmacogenomics to further advance the treatment of human cancers, with childhood leukemia serving as a paradigm.

摘要

在过去的四十年里,儿童急性白血病的治疗取得了显著进展,这种疾病从曾经致命发展到如今急性淋巴细胞白血病治愈率达80%,急性髓系白血病治愈率达45%。这一进展很大程度上归功于现有治疗方式的优化,而非新药物的发现。然而,初始治疗后复发的白血病患者年数量仍高于大多数儿童癌症的新发病例数。药物遗传学的目的是制定策略,使药物个性化并为个体患者量身定制治疗方案,目标是通过更好地了解个体的基因构成来提高疗效和安全性。在本综述中,我们总结了近期与儿童急性白血病治疗相关的药物基因组学研究。这些研究包括使用候选基因方法的工作,以及使用单倍型图谱和基因表达谱分析的全基因组研究。这些策略表明药物基因组学有望进一步推动人类癌症的治疗,儿童白血病就是一个范例。

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