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评价 G-CSF 诱导在强化诱导化疗后自体造血干细胞移植治疗老年急性髓系白血病中的前瞻性随机试验的长期结果。

Long-term results of a prospective randomized trial evaluating G-CSF priming in intensive induction chemotherapy followed by autologous stem cell transplantation in elderly patients with acute myeloid leukemia.

机构信息

Department of Medicine II, Hematology/Oncology, University Hospital Frankfurt, Frankfurt, Germany.

出版信息

Ann Hematol. 2014 Feb;93(2):193-202. doi: 10.1007/s00277-013-1873-3. Epub 2013 Aug 27.

Abstract

Few studies have evaluated granulocyte colony-stimulating factor (G-CSF) priming in elderly patients with intensively treated acute myeloid leukemia (AML), and no data are available for genetically defined AML subgroups. We provide long-term results (median follow-up 7.6 years) of a randomized trial in which 183 patients (median age 67 years) received G-CSF prior to (G-CSF priming) or after two cycles of induction chemotherapy. CR rates with G-CSF priming and G-CSF post-chemotherapy were comparable (57 vs. 67 %, p = 0.153), with overall survival (OS) probabilities of 14 vs. 17 % at 10 years. Induction mortality was significantly higher with G-CSF priming (23 vs. 10 %, p = 0.015), primarily in normal karyotype (NK) AML. In this subgroup, a trend for better relapse-free survival (RFS) was observed with G-CSF priming (44 vs. 22 % at 10 years, p = 0.074) but did not translate into an OS benefit. G-CSF priming had no impact on AML with FLT3-ITD and NPM mutations and did not improve outcome in patients with adverse cytogenetics. In a landmark analysis, late consolidation with autologous stem cell transplantation or a second consolidation cycle significantly improved RFS compared with one consolidation cycle (21.0 vs. 12.8 months, p = 0.046). Future studies on G-CSF priming should be restricted to NK AML and used only in post-remission therapy.

摘要

鲜有研究评估过在接受强化治疗的老年急性髓系白血病(AML)患者中使用粒细胞集落刺激因子(G-CSF)预处理,也没有针对基因定义的 AML 亚组的数据。我们提供了一项随机试验的长期结果(中位随访 7.6 年),该试验中 183 例患者(中位年龄 67 岁)在接受两个周期诱导化疗之前(G-CSF 预处理)或之后接受 G-CSF。G-CSF 预处理和 G-CSF 化疗后 CR 率相当(57%比 67%,p=0.153),10 年时总生存(OS)概率分别为 14%和 17%。G-CSF 预处理的诱导死亡率显著更高(23%比 10%,p=0.015),主要发生在核型正常(NK)AML 中。在这个亚组中,G-CSF 预处理有更好的无复发生存(RFS)趋势(10 年时分别为 44%和 22%,p=0.074),但并没有转化为 OS 获益。G-CSF 预处理对伴有 FLT3-ITD 和 NPM 突变的 AML 没有影响,也不能改善不良细胞遗传学患者的预后。在一项里程碑式的分析中,与一个巩固周期相比,自体干细胞移植或第二个巩固周期的晚期巩固显著改善了 RFS(21.0 个月比 12.8 个月,p=0.046)。未来的 G-CSF 预处理研究应仅限于 NK-AML,并仅用于缓解后治疗。

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