摘要
急性早幼粒细胞白血病(APL)是急性白血病的一种特殊类型,近几十年来由于蒽环类化疗药物、全反式维甲酸和砷剂的使用,其治愈率得到了明显的提高,现代化的分层治疗进一步提高了疗效并减少了治疗相关不良反应。文章回顾了全反式维甲酸、砷剂进入临床应用的历史,从疾病特征、全反式维甲酸和砷剂的治疗现状、治疗机制及耐药机制等方面作一介绍。
Acute promyelocytic leukemia (APL) is a special type of acute leukemia. The cure rate of APL has been significantly improved in the past decades due to the use of anthracyclines, all-trans retinoic acid and arsenic. Modern stratified treatment of APL further enhances the therapeutic efficacy and reduces the treatment-related toxicity. This article reviews the history of all-trans retinoic acid and arsenic into clinical application, and the characteristics of disease, treatment status of all-trans retinoic acid and arsenic, treatment mechanism and drug resistance mechanism in APL are introduced.
作者
刘福佳
沈杨
Liu Fujia;Shen Yang(Department of Hematology, Ruijin Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai 200025, China)
出处
《白血病.淋巴瘤》
CAS
2019年第9期546-549,共4页
Journal of Leukemia & Lymphoma
关键词
白血病
早幼粒细胞
急性
维甲酸
砷剂
药理作用分子作用机制
耐药机制
Leukemia, promyelocytic, acute
Retinoic acid
Arsenical
Molecular mechanisms of pharmacological action
Drug-resistance mechanisms