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回顾性比较新诊断的核心结合因子(CBF)急性髓系白血病患者接受 Fludarabine、Cytarabine、GCSF(FLAG)联合 gemtuzumab ozogamicin(GO)或 Idarubicin(IDA)治疗的生存和反应:MD Anderson 经验 174 例患者。

Retrospective comparison of survival and responses to Fludarabine, Cytarabine, GCSF (FLAG) in combination with gemtuzumab ozogamicin (GO) or Idarubicin (IDA) in patients with newly diagnosed core binding factor (CBF) acute myelogenous leukemia: MD Anderson experience in 174 patients.

机构信息

Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.

Department of Hematopathology, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.

出版信息

Am J Hematol. 2022 Nov;97(11):1427-1434. doi: 10.1002/ajh.26700. Epub 2022 Sep 27.

Abstract

Fludarabine, cytarabine, GCSF (FLAG)-based induction/consolidation results in high remission rates in core binding factor (CBF) acute myelogenous leukemia. We treated 174 consecutive patients with newly diagnosed CBF-AML in a prospective clinical trial of FLAG-based induction/consolidation in combination with gemtuzumab ozogamicin (FLAG-GO; N = 65) or in combination with idarubicin (FLAG-IDA; N = 109). The 5 year RFS in the FLAG-GO cohort was significantly better than the FLAG-IDA cohort, 78% versus 59%, respectively (p-value = .02). In multivariate analysis for RFS, age (p = .0001), FLAG-GO regimen (p = .04), 4 log reduction in CBF-related fusion transcript by quantitative polymerase chain reaction (qPCR) in bone marrow samples at end of consolidation therapy (p = .03), and additional cytogenetic abnormalities (p = .03) were significant variables. Lower age (p = .0001) and 3 log or more transcript reduction at end of induction (p = .04) were significant variables predicting for better overall survival (OS), while there was strong trend for better OS with FLAG-GO (p = .06) regimen. FLAG-GO regimen was superior in optimal disease specific fusion transcript reduction at end of induction (p = .002), mid-consolidation (p < .01), and end of consolidation (p < .001) therapy. Induction/consolidation with FLAG-GO regimen results in better clinical outcomes in newly diagnosed patients with CBF-AML compared to FLAG-IDA and achieves deeper molecular clearance by qPCR assessment of the fusion transcripts.

摘要

氟达拉滨、阿糖胞苷、粒细胞集落刺激因子(GCSF)(FLAG)为基础的诱导/巩固治疗可使核心结合因子(CBF)急性髓细胞白血病获得高缓解率。我们在一项前瞻性临床试验中用 FLAG 为基础的诱导/巩固治疗联合吉妥珠单抗奥佐米星(FLAG-GO;N=65)或联合伊达比星(FLAG-IDA;N=109)治疗了 174 例新诊断的 CBF-AML 患者。FLAG-GO 组的 5 年 RFS 明显优于 FLAG-IDA 组,分别为 78%和 59%(p 值=0.02)。多变量分析显示,RFS 的预后因素包括年龄(p=0.0001)、FLAG-GO 方案(p=0.04)、巩固治疗结束时骨髓样本中 CBF 相关融合转录物定量聚合酶链反应(qPCR)4 对数减少(p=0.03)和额外的细胞遗传学异常(p=0.03)。年龄较小(p=0.0001)和诱导结束时转录物减少 3 个对数(p=0.04)是预测总生存期(OS)更好的显著变量,而 FLAG-GO 方案有更好 OS 的趋势(p=0.06)。FLAG-GO 方案在诱导结束时(p=0.002)、中期巩固(p<0.01)和巩固结束时(p<0.001)获得了更好的疾病特异性融合转录物减少,优于 FLAG-IDA 方案。与 FLAG-IDA 相比,FLAG-GO 方案在新诊断的 CBF-AML 患者中诱导/巩固治疗可获得更好的临床结局,并通过 qPCR 评估融合转录物实现更深的分子清除。

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