Kornblau Steven M, Banker Deborah E, Stirewalt Derek, Shen Danny, Lemker Elizabeth, Verstovsek Srdan, Estrov Zeev, Faderl Stefan, Cortes Jorge, Beran Miloslav, Jackson C Ellen, Chen Wenjing, Estey Elihu, Appelbaum Frederick R
Section of Molecular Hematology and Therapy, Department of Stem Cell Transplantation and Cellular Therapy, The University of Texas M. D. Anderson Cancer Center, Houston 77030-4009, USA.
Blood. 2007 Apr 1;109(7):2999-3006. doi: 10.1182/blood-2006-08-044446.
Following exposure to cytotoxic agents, acute myeloid leukemia (AML) blasts elevate cellular cholesterol in a defensive adaptation that increases chemoresistance, but blockade of HMG-CoA reductase with statins restores chemosensitivity in vitro. This phase 1 study evaluated adding pravastatin (PV) (40-1680 mg/day, days 1-8) to idarubicin (Ida) ([12 mg/ (M2 x day), days 4-6]) + high-dose cytarabine (Ara-C; HDAC) [1.5 g/(M2 x day) by CI, days 4-7] in 15 newly diagnosed and 22 salvage patients with unfavorable (n = 26) or intermediate (n = 10) prognosis cytogenetics. Compared with historical experience with Ida-HDAC, the duration of neutropenia and throbmbocytopenia and the toxicity profile were unaffected by the addition of PV. During PV loading (day 0-4) serum triglyceride and total and LDL cholesterol levels decreased in nearly all patients. Pharmacokinetic studies demonstrated higher and more sustained serum PV levels with PV doses above 1280 mg/day. CR/CRp was obtained in 11 of 15 new patients, including 8 of 10 with unfavorable cytogenetics, and 9 of 22 salvage patients. An MTD for PV + Ida-HDAC was not reached. Addition of PV to Ida-HDAC was safe, and the encouraging response rates support conducting further trials evaluating the effect of cholesterol modulation on response in AML.
暴露于细胞毒性药物后,急性髓系白血病(AML)原始细胞会通过一种防御性适应机制提高细胞胆固醇水平,从而增加化疗耐药性,但在体外使用他汀类药物阻断HMG-CoA还原酶可恢复化疗敏感性。这项1期研究评估了在15例新诊断和22例挽救性治疗的患者中,将普伐他汀(PV)(40 - 1680 mg/天,第1 - 8天)添加到伊达比星(Ida)([12 mg/(M2×天),第4 - 6天])+大剂量阿糖胞苷(Ara-C;HDAC)[1.5 g/(M2×天)持续静脉输注,第4 - 7天]的方案中,这些患者具有不良(n = 26)或中等(n = 10)预后的细胞遗传学特征。与伊达比星 - HDAC的既往经验相比,中性粒细胞减少和血小板减少的持续时间以及毒性特征并未因添加PV而受到影响。在PV负荷期(第0 - 4天),几乎所有患者的血清甘油三酯、总胆固醇和低密度脂蛋白胆固醇水平均下降。药代动力学研究表明,PV剂量高于1280 mg/天时,血清PV水平更高且更持久。15例新患者中有11例获得完全缓解/部分血液学恢复(CR/CRp),其中10例具有不良细胞遗传学特征的患者中有8例,22例挽救性治疗患者中有9例。未达到PV +伊达比星 - HDAC的最大耐受剂量(MTD)。在伊达比星 - HDAC中添加PV是安全可靠的,令人鼓舞的缓解率支持开展进一步试验,以评估胆固醇调节对AML缓解的影响。