Becker Pamela S, Medeiros Bruno C, Stein Anthony S, Othus Megan, Appelbaum Frederick R, Forman Stephen J, Scott Bart L, Hendrie Paul C, Gardner Kelda M, Pagel John M, Walter Roland B, Parks Cynthia, Wood Brent L, Abkowitz Janis L, Estey Elihu H
Division of Hematology, Department of Medicine, University of Washington, Seattle, Washington; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Am J Hematol. 2015 Apr;90(4):295-300. doi: 10.1002/ajh.23927. Epub 2015 Jan 30.
Prior study of the combination of clofarabine and high dose cytarabine with granulocyte colony-stimulating factor (G-CSF) priming (GCLAC) in relapsed or refractory acute myeloid leukemia resulted in a 46% rate of complete remission despite unfavorable risk cytogenetics. A multivariate analysis demonstrated that the remission rate and survival with GCLAC were superior to FLAG (fludarabine, cytarabine, G-CSF) in the relapsed setting. We therefore initiated a study of the GCLAC regimen in the upfront setting in a multicenter trial. The objectives were to evaluate the rates of complete remission (CR), overall and relapse-free survival (OS and RFS), and toxicity of GCLAC. Clofarabine was administered at 30 mg m(-2) day(-1) × 5 and cytarabine at 2 g m(-2) day(-1) × 5 after G-CSF priming in 50 newly-diagnosed patients ages 18-64 with AML or advanced myelodysplastic syndrome (MDS) or advanced myeloproliferative neoplasm (MPN). Responses were assessed in the different cytogenetic risk groups and in patients with antecedent hematologic disorder. The overall CR rate was 76% (95% confidence interval [CI] 64-88%) and the CR + CRp (CR with incomplete platelet count recovery) was 82% (95% CI 71-93%). The CR rate was 100% for patients with favorable, 84% for those with intermediate, and 62% for those with unfavorable risk cytogenetics. For patients with an antecedent hematologic disorder (AHD), the CR rate was 65%, compared to 85% for those without an AHD. The 60 day mortality was 2%. Thus, front line GCLAC is a well-tolerated, effective induction regimen for AML and advanced myelodysplastic or myeloproliferative disorders.
先前针对复发或难治性急性髓系白血病开展的一项研究,将氯法拉滨与高剂量阿糖胞苷联合使用,并采用粒细胞集落刺激因子(G-CSF)预激(GCLAC)方案,结果显示,尽管细胞遗传学风险不利,但完全缓解率仍达46%。多变量分析表明,在复发情况下,GCLAC方案的缓解率和生存率优于FLAG(氟达拉滨、阿糖胞苷、G-CSF)方案。因此,我们在一项多中心试验中启动了GCLAC方案用于初始治疗的研究。目的是评估完全缓解(CR)率、总生存率和无复发生存率(OS和RFS)以及GCLAC方案的毒性。在50例年龄为18 - 64岁、新诊断为急性髓系白血病(AML)或晚期骨髓增生异常综合征(MDS)或晚期骨髓增殖性肿瘤(MPN)的患者中,经G-CSF预激后,给予氯法拉滨30 mg m(-2) 每日1次×5天,阿糖胞苷2 g m(-2) 每日1次×5天。对不同细胞遗传学风险组以及有既往血液系统疾病的患者的反应进行了评估。总CR率为76%(95%置信区间[CI] 64 - 88%),CR + CRp(血小板计数未完全恢复的CR)为82%(95% CI 71 - 93%)。细胞遗传学风险良好的患者CR率为100%,中等风险的患者为84%,不良风险的患者为62%。有既往血液系统疾病(AHD)的患者CR率为65%,无AHD的患者为85%。60天死亡率为2%。因此,一线GCLAC方案是一种耐受性良好、有效的AML及晚期骨髓增生异常或骨髓增殖性疾病诱导方案。