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首页> 外文期刊>European Journal of Haematology >Treatment patterns and healthcare resource utilization in patients with FLT3 FLT3 ‐mutated and wild‐type acute myeloid leukemia: A medical chart study
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Treatment patterns and healthcare resource utilization in patients with FLT3 FLT3 ‐mutated and wild‐type acute myeloid leukemia: A medical chart study

机译:FLT3 FLT3患者的治疗模式和医疗保健资源利用和野生型急性髓性白血病:医学图表研究

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摘要

Abstract Objectives To assess real‐world treatment patterns and healthcare resource utilization (HRU) among patients with FLT3 –mutated ( FLT3 mut ) and FLT3 –wild‐type ( FLT3 wt ) acute myeloid leukemia (AML). Methods Data were abstracted from medical charts of patients with AML from 10 countries. Patients were grouped based on their FLT3 mutation status, age (18‐64 or ≥65), and whether they were newly diagnosed (ND) or relapsed/refractory (R/R). Results Charts of 1027 AML patients were included (183 FLT3 mut 18‐64 ND; 136 FLT3 mut ≥65 ND; 181 FLT3 mut R/R; 186 FLT3 wt 18‐64 ND; 159 FLT3 wt ≥65 ND; 182 FLT3 wt R/R). Substantial heterogeneity was observed in treatment patterns for AML. Among ND patients 18‐64, the most common initial treatment was standard‐to‐intermediate dose cytarabine‐based therapies (43.2% for FLT3 mut and 55.9% for FLT3 wt ); among ND patients ≥65, the most common initial treatment was hypomethylating agent‐based therapies (36.0% and 47.2%). Among R/R patients, the most common initial treatment after R/R was best supportive care only (39.8% and 24.7%). HRU was substantial across cohorts during both event‐free and post‐event periods. Conclusions Treatment patterns of AML were heterogeneous and FLT3 mut AML was treated more aggressively than FLT3 wt disease. HRU was substantial for all cohorts, particularly after relapse or treatment failure.
机译:摘要目的,以评估FLT3 - 审查(FLT3 MUT)和FLT3-WILD型(FLT3 WT)急性髓性白血病(AML)患者的真实治疗模式和医疗保健资源利用(HRU)。方法数据从10个国家的AML患者的医学图表中抽象出来。患者基于其FLT3突变状态,年龄(18-64或≥65)进行分组,以及它们是否被新诊断出(ND)或复发/难治(R / R)。结果包括1027例AML患者的图表(183 FLT3 MUT 18-64 ND; 136 FLT3MUT≥65ND; 181 FLT3 MUT R / R; 186 FLT3 WT 18-64 ND; 159 FLT3WT≥65ND; 182 FLT3 WT R / r)。在AML的治疗模式中观察到实质性异质性。在ND患者18-64中,最常见的初始治疗是基于标准的中间剂量的含水酸碱基疗法(FLT3 mut的43.2%,FLT3重量为55.9%);在ND患者≥65中,最常见的初始治疗是基于低甲基化剂的疗法(36.0%和47.2%)。在R / R患者中,R / R后最常见的初始治疗仅适用于最佳支持性护理(39.8%和24.7%)。在无事件和活动期间,HRU在群组中很大程度上是跨国队的群体。结论AML的处理模式是异质的,并且比FLT3 WT病更富有焦化的FLT3 mut AML。 Hru对所有队列很重要,特别是在复发或治疗失败后。

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