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