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首页> 外文期刊>Frontiers in Oncology >Phase I Trial of Lithium and Tretinoin for Treatment of Relapsed and Refractory Non-promyelocytic Acute Myeloid Leukemia
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Phase I Trial of Lithium and Tretinoin for Treatment of Relapsed and Refractory Non-promyelocytic Acute Myeloid Leukemia

机译:锂和维甲酸锂试验治疗复发和难治性非幼幼胞细胞急性髓性白血病的治疗

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Glycogen synthase kinase-3 (GSK3) inhibitors induce differentiation and growth inhibition of acute myeloid leukemia (AML) cells. Our pre-clinical studies showed GSK3 inhibition leads to sensitization of AML cells to tretinoin-mediated differentiation. We conducted a phase I trial of lithium, a GSK3 inhibitor, plus tretinoin for relapsed, refractory non-promyelocytic AML. Nine patients with median (range) age 65 (42–82) years were enrolled. All subjects had relapsed leukemia after prior therapy, with a median (range) of 3 (1–3) prior therapies. Oral lithium carbonate 300 mg was given 2–3 times daily and adjusted to meet target serum concentration (0.6 to 1.0 mmol/L); tretinoin 22.5 or 45 mg/m ~(2)/day (two equally divided doses) was administered orally on days 1–7 and 15–21 of a 28-day cycle. Four patients attained disease stability with no increase in circulating blasts for ≥4 weeks. Median (range) survival was 106 days (60–502). Target serum lithium concentration was achieved in all patients and correlated with GSK3 inhibition in leukemic cells. Immunophenotypic changes associated with myeloid differentiation were observed in five patients. The combination treatment led to a reduction in the CD34+ CD38– AML stem cell population both in vivo and in vitro . The combination of lithium and tretinoin is well-tolerated, induces differentiation of leukemic cells, and may target AML stem cells, but has limited clinical activity in the absence of other antileukemic agents. The results of this clinical trial suggest GSK3 inhibition can result in AML cell differentiation and may be a novel therapeutic strategy in this disease, particularly in combination with other antileukemic agents. Lithium is a weak GSK3 inhibitor and future strategies in AML treatment will probably require more potent agents targeting this pathway or combinations with other antileukemic agents. This trial is registered at ClinicalTrials.gov NCT01820624.
机译:糖原合成酶激酶-3(GSK3)抑制剂诱导急性髓性白血病(AML)细胞的分化和生长抑制。我们的临床前研究表明,GSK3抑制导致AML细胞的敏化对Tretinionin介导的分化。我们进行了一期锂,GSK3抑制剂,加甘氨酸的锂试验,用于复发,难治性非临时织造菌AML。九名中位数(范围)65岁(42-82)年的患者报名参加。所有受试者均已疗法后复发白血病,中位数(范围)为3(1-3)疗法。每天给予口服碳酸盐300mg,得到2-3次,并调整以满足靶血清浓度(0.6至1.0mmol / L);在28天循环的第1-7天和15-21天,口服施用维甲酸丁二醇酯22.5或45mg / m〜(2)/天(两种等分分开的剂量)。四名患者达到疾病稳定性,循环爆炸率没有增加≥4周。中位数(范围)存活率为106天(60-502)。在所有患者中达到靶血清锂浓度,并与白血病细胞中的GSK3抑制相关。在五名患者中观察到与骨髓分化相关的免疫型变化。组合处理导致体内和体外CD34 + CD38-AML干细胞群的降低。锂和维甲酯的组合是耐受良好耐受的,诱导白血病细胞的分化,并且可以靶向AML干细胞,但在没有其他抗血清血症药物的情况下具有有限的临床活性。该临床试验的结果表明GSK3抑制可以导致AML细胞分化,并且可以是这种疾病的新治疗策略,特别是与其他抗血糖药物组合。锂是一种弱GSK3抑制剂和AML治疗中的未来策略可能需要更有效的药剂靶向该途径或与其他抗血糖药物的组合。该试验在ClinicalTrials.gov NCT01820624注册。

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