Department of Hematology, Medical University of Lodz, Lodz, Poland.
Department of Hematology, Institute of Hematology and Transfusion Medicine, Warsaw, Poland.
Am J Hematol. 2017 Apr;92(4):359-366. doi: 10.1002/ajh.24654. Epub 2017 Feb 13.
Intensive induction chemotherapy using anthracycline and cytarabine backbone is considered the most effective upfront therapy in physically fit older patients with acute myeloid leukemia (AML). However, outcomes of the standard induction in elderly AML are inferior to those observed in younger patients, and they are still unsatisfactory. As addition of cladribine to the standard induction therapy is known to improve outcome in younger AML patients. The present randomized phase II study compares efficacy and toxicity of the DAC (daunorubicin plus cytarabine plus cladribine) regimen with the standard DA (daunorubicin plus cytarabine) regimen in the newly diagnosed AML patients over 60 years of age. A total of 171 patients were enrolled in the study (DA, 86; DAC, 85). A trend toward higher complete remission (CR) was observed in the DAC arm compared to the DA arm (44% vs. 34%; P = .19), which did not lead to improved median overall survival, which in the case of the DAC group was 8.6 months compared to in 9.1 months in the DA group (P = .64). However, DAC appeared to be superior in the group of patients aged 60-65 (CR rate: DAC 51% vs. DA 29%; P = .02). What is more, a subgroup of patients, with good and intermediate karyotypes, benefited from addition of cladribine also in terms of overall survival (P = .02). No differences in hematological and nonhematological toxicity between the DA and DAC regimens were observed.
在身体状况良好的老年急性髓细胞白血病 (AML) 患者中,使用蒽环类药物和阿糖胞苷为基础的强化诱导化疗被认为是最有效的一线治疗方法。然而,老年 AML 患者接受标准诱导治疗的结果不如年轻患者,而且仍然不尽如人意。已知在标准诱导治疗中添加克拉屈滨可改善年轻 AML 患者的预后。本随机 II 期研究比较了在新诊断的 60 岁以上 AML 患者中,DAC(柔红霉素+阿糖胞苷+克拉屈滨)方案与标准 DA(柔红霉素+阿糖胞苷)方案的疗效和毒性。共有 171 名患者入组本研究(DA 组 86 例;DAC 组 85 例)。与 DA 组相比,DAC 组的完全缓解(CR)率呈上升趋势(44%比 34%;P=0.19),但并未导致中位总生存期改善,DAC 组的中位总生存期为 8.6 个月,而 DA 组为 9.1 个月(P=0.64)。然而,DAC 在 60-65 岁年龄组的患者中似乎更具优势(CR 率:DAC 组为 51%,DA 组为 29%;P=0.02)。此外,对于具有良好和中等核型的亚组患者,添加克拉屈滨也可改善总体生存(P=0.02)。DA 和 DAC 方案之间在血液学和非血液学毒性方面无差异。