外显子组测序
癌症的体细胞进化
医学
髓系白血病
髓样
癌症
外显子组
化疗
疾病
肿瘤科
内科学
白血病
阿糖胞苷
突变
免疫学
基因
生物
遗传学
作者
Philipp A. Greif,Luise Hartmann,Sebastian Vosberg,Sophie M. Stief,Raphael Mattes,Ines Hellmann,Klaus H. Metzeler,Tobias Herold,Stefanos A. Bamopoulos,Paul Kerbs,Vindi Jurinović,Daniela Schumacher,Friederike Pastore,Kathrin Bräundl,Evelyn Zellmeier,Bianka Ksienzyk,Nikola P. Konstandin,Stephanie Schneider,Alexander Graf,Stefan Krebs
标识
DOI:10.1158/1078-0432.ccr-17-2344
摘要
Purpose: To study mechanisms of therapy resistance and disease progression, we analyzed the evolution of cytogenetically normal acute myeloid leukemia (CN-AML) based on somatic alterations.Experimental Design: We performed exome sequencing of matched diagnosis, remission, and relapse samples from 50 CN-AML patients treated with intensive chemotherapy. Mutation patterns were correlated with clinical parameters.Results: Evolutionary patterns correlated with clinical outcome. Gain of mutations was associated with late relapse. Alterations of epigenetic regulators were frequently gained at relapse with recurring alterations of KDM6A constituting a mechanism of cytarabine resistance. Low KDM6A expression correlated with adverse clinical outcome, particularly in male patients. At complete remission, persistent mutations representing preleukemic lesions were observed in 48% of patients. The persistence of DNMT3A mutations correlated with shorter time to relapse.Conclusions: Chemotherapy resistance might be acquired through gain of mutations. Insights into the evolution during therapy and disease progression lay the foundation for tailored approaches to treat or prevent relapse of CN-AML. Clin Cancer Res; 24(7); 1716-26. ©2018 AACR.
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