癸他滨
阿糖胞苷
医学
髓系白血病
内科学
养生
阿扎胞苷
低甲基化剂
不利影响
肿瘤科
胃肠病学
白血病
DNA甲基化
生物
基因表达
基因
生物化学
作者
Annie Im,Kevin Quann,Mounzer Agha,Anastasios Raptis,Robert L. Redner,Jing‐Zhou Hou,Rafic Farah,Kathleen A. Dorritie,Alison R. Sehgal,Daniel P. Normolle,Dana H. Bovbjerg,Nidhi Aggarwal,James G. Herman,Konstantinos Lontos,Michael Boyiadzis
摘要
Abstract Acute myeloid leukemia (AML) in older patients has a poor prognosis, low complete remission (CR) rates, and poor overall survival (OS). Preclinical studies have shown synergistic effects of epigenetic priming with hypomethylating agents followed by cytarabine. Based on these data, we hypothesized that an induction regimen using epigenetic priming with decitabine, followed by cytarabine would be effective and safe in older patients with previously untreated AML. Here, we conducted a phase 2 trial in which older patients with previously untreated AML received an induction regimen consisting of 1 or 2 courses of decitabine 20 mg/m 2 intravenously (IV) for 5 days followed by cytarabine 100 mg/m 2 continuous IV infusion for 5 days. Forty‐four patients (median age 76 years) were enrolled, and CR/CRi was achieved by 26 patients (59% of all patients, 66.7% of evaluable patients). Fourteen of 21 (66.7%) patients with adverse cytogenetics achieved CR including six out of seven evaluable patients with TP53 mutations. The 4‐ and 8‐week mortality rates were 2.3% and 9.1%, respectively, with median OS of 10.7 months. These results suggest epigenetic priming with decitabine followed by cytarabine should be considered as an option for first‐line therapy in older patients with AML. This trial was registered at www.clinicaltrials.gov as # NCT01829503.
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