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基于外周血原始细胞清除率的新型 idarubicin 和 cytarabine 联合高三尖杉酯碱诱导方案治疗初诊急性髓系白血病患者的优化:单臂、Ⅱ期临床试验(RJ-AML 2014)。

Optimization of idarubicin and cytarabine induction regimen with homoharringtonine for newly diagnosed acute myeloid leukemia patients based on the peripheral blast clearance rate: A single-arm, phase 2 trial (RJ-AML 2014).

机构信息

Shanghai Institute of Hematology, State Key Laboratory of Medical Genomics, National Research Center for Translational Medicine at Shanghai, Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China.

出版信息

Am J Hematol. 2022 Jan 1;97(1):43-51. doi: 10.1002/ajh.26386. Epub 2021 Nov 1.

Abstract

Individualized chemotherapy, which is at the forefront of acute myeloid leukemia (AML) treatment, has moderately improved outcomes over the past decade. Monitoring the peripheral blood blast burden during induction by flow cytometry has shown significant value in the evaluation of treatment responses. Our previous study reported the day 5 peripheral blast clearance rate (D5-PBCR) as an indicator of early treatment response, and D5-PBCR (+) patients showed poor outcomes. We performed the present phase 2 trial of early intervention in D5-PBCR (+) patients with homoharringtonine (HHT) introduced in the traditional induction regimen with anthracycline and cytarabine. The primary endpoint was complete remission (CR). This study enrolled 151 patients, 65 patients were D5-PBCR (+) and 55 patients completed induction with HHT addition. The overall CR rate after one course of induction was 84.4%, with 87.5% and 80.0% for the D5-PBCR (-) and D5-PBCR (+) groups, respectively. The incidence of grade 3/4 adverse events was comparable between the two groups. At the median follow-up of 53.1 months, median overall survival (OS) was not reached in the entire cohort, and median event-free survival (EFS) was 42.2 months. Neither the OS nor EFS showed significant differences between the D5-PBCR (-) and D5-PBCR (+) groups. Compared to historical data, significant improvements in both OS (p = .020) and EFS (p = .020) were observed in the D5-PBCR (+) group. In conclusion, optimization of induction chemotherapy with idarubicin and cytarabine according to D5-PBCR is feasible in patients with newly diagnosed AML. The addition of HHT demonstrated a good efficacy and safety profile.

摘要

个体化化疗是急性髓系白血病(AML)治疗的前沿,在过去十年中,其治疗结果得到了适度改善。通过流式细胞术监测诱导期外周血 blast 负荷在评估治疗反应方面显示出了重要价值。我们之前的研究报告了第 5 天外周血 blast 清除率(D5-PBCR)作为早期治疗反应的指标,D5-PBCR(+)患者的预后较差。我们在蒽环类药物和阿糖胞苷的传统诱导方案中加入高三尖杉酯碱(HHT),对 D5-PBCR(+)患者进行了早期干预的 II 期临床试验。主要终点是完全缓解(CR)。这项研究纳入了 151 例患者,其中 65 例患者为 D5-PBCR(+),55 例患者完成了诱导治疗并添加了 HHT。一疗程诱导后的总 CR 率为 84.4%,D5-PBCR(-)和 D5-PBCR(+)组的 CR 率分别为 87.5%和 80.0%。两组的 3/4 级不良事件发生率相当。在中位随访 53.1 个月时,整个队列的中位总生存期(OS)尚未达到,中位无事件生存期(EFS)为 42.2 个月。D5-PBCR(-)和 D5-PBCR(+)组的 OS 和 EFS 均无显著差异。与历史数据相比,D5-PBCR(+)组的 OS(p=0.020)和 EFS(p=0.020)均有显著改善。总之,根据 D5-PBCR 优化伊达比星和阿糖胞苷的诱导化疗在新诊断的 AML 患者中是可行的。HHT 的加入显示出良好的疗效和安全性。

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