Department of Pediatrics, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, PR China.
Mediterr J Hematol Infect Dis. 2012;4(1):e2012012. doi: 10.4084/MJHID.2012.012. Epub 2012 Mar 10.
Acute promyelocytic leukemia (APL) is the subtype of acute myeloid leukemia characterized by an accumulation of abnormal promyelocytes in bone marrow, a severe bleeding tendency and the presence of the chromosomal translocation t(15;17) or variants. APL, the most fatal type of leukemia two decades ago, is highly curable with current treatment strategies. There is evidence that the incidence of APL varies across ethnic groups and that genetic factors play a role in the etiology of APL. And there are some difference between children and adults in APL.1-3 The limited data of children available in many developing countries suggest that the rate of early mortality is high and that long-term survival is poor. Death from bleeding and infection during chemotherapy, relapse and treatment abandonment are among the main cause of treatment failure in APL children as well in adults.2 The status of children APL treatment in China has not been described in general.Here we describe the epidemiology and treatment of APL in children in China. In addition, we review the results of a survey of its clinical manifestations and outcome in China.
急性早幼粒细胞白血病(APL)是急性髓细胞白血病的一个亚型,其特征是骨髓中异常早幼粒细胞的积累、严重的出血倾向以及存在染色体易位 t(15;17)或其变体。APL 是二十年前最致命的白血病类型,但目前的治疗策略可以高度治愈。有证据表明,APL 的发病率在不同种族之间存在差异,遗传因素在 APL 的发病机制中起作用。并且 APL 在儿童和成人之间存在一些差异。1-3 在许多发展中国家,儿童的可用数据有限,这表明早期死亡率高,长期生存率低。在化疗期间因出血和感染、复发以及治疗中断而死亡是儿童和成人 APL 治疗失败的主要原因之一。2 中国儿童 APL 的治疗情况尚未全面描述。在这里,我们描述了中国儿童 APL 的流行病学和治疗情况。此外,我们还回顾了中国对其临床表现和结果的调查结果。