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依托泊苷治疗噬血细胞性淋巴组织细胞增生症后发生的继发性急性髓系白血病。

Secondary acute myeloid leukemia after etoposide therapy for haemophagocytic lymphohistiocytosis.

作者信息

RamaChandran Shanti, Ariffin Hany

机构信息

Department of Paediatrics, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.

出版信息

Pediatr Blood Cancer. 2009 Sep;53(3):488-90. doi: 10.1002/pbc.22063.

Abstract

Haemophagocytic lymphohistiocytosis (HLH) is an uncommon disease with a high fatality rate. Etoposide is an important component of current HLH treatment regimes. Two patients with HLH developed etoposide-related secondary acute myeloid leukemia (sAML) following therapy for HLH. Etoposide, an epipodophyllotoxin, is a topoisomerase II inhibitor that interacts with DNA to potentiate leukaemogenesis. The risk of developing sAML is estimated to be between 1% and 5%, 2-20 years after exposure to etoposide but may also be related to cumulative drug doses, treatment schedules, host factors and co-administration of other antineoplastic agents.

摘要

噬血细胞性淋巴组织细胞增生症(HLH)是一种死亡率很高的罕见疾病。依托泊苷是当前HLH治疗方案的重要组成部分。两名HLH患者在接受HLH治疗后发生了依托泊苷相关的继发性急性髓系白血病(sAML)。依托泊苷是一种表鬼臼毒素,是一种拓扑异构酶II抑制剂,它与DNA相互作用以增强白血病发生。发生sAML的风险估计在1%至5%之间,发生在接触依托泊苷后的2至20年,但也可能与累积药物剂量、治疗方案、宿主因素以及其他抗肿瘤药物的联合使用有关。

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