医学
髓系白血病
重症监护医学
临床试验
儿童白血病
微小残留病
疾病
肿瘤科
药物治疗
髓样
白血病
儿科
内科学
淋巴细胞白血病
出处
期刊:Pediatric Drugs
[Springer Nature]
日期:2017-02-01
卷期号:19 (1): 1-10
被引量:49
标识
DOI:10.1007/s40272-016-0200-6
摘要
The outcome for children with acute myeloid leukemia (AML) has improved significantly over the past 30 years, with complete remission and overall survival rates exceeding 90 and 60%, respectively, in recent clinical trials. However, these improvements have not been achieved by the introduction of new agents. Instead, intensification of standard chemotherapy, more precise risk classification, improvements in supportive care, and the use of minimal residual disease to monitor response to therapy have all contributed to this success. Nevertheless, novel therapies are needed, as the cure rates for many subtypes of childhood AML remain unacceptably low. Here, we briefly review advances in our understanding of the biology and genetics of AML, the results of recent clinical trials, and current recommendations for the treatment of children with AML.
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