Evolution of Cytogenetically Normal Acute Myeloid Leukemia During Therapy and Relapse: An Exome Sequencing Study of 50 Patients

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
出处
期刊:Clinical Cancer Research [American Association for Cancer Research]
卷期号:24 (7): 1716-1726 被引量:80
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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