首页> 外文期刊>Journal of Hematology and Oncology >Busulfan plus fludarabine as a myeloablative conditioning regimen compared with busulfan plus cyclophosphamide for acute myeloid leukemia in first complete remission undergoing allogeneic hematopoietic stem cell transplantation: a prospective and multicen
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Busulfan plus fludarabine as a myeloablative conditioning regimen compared with busulfan plus cyclophosphamide for acute myeloid leukemia in first complete remission undergoing allogeneic hematopoietic stem cell transplantation: a prospective and multicen

机译:与白消安加环磷酰胺相比,白消安加氟达拉滨是一种急性清髓治疗方案,用于同种异体造血干细胞移植首次完全缓解的急性髓细胞性白血病:前瞻性和多方面

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Objective We conducted a prospective, randomized, open-label, multicenter study to compare busulfan plus fludarabine (BuFlu) with busulfan plus cyclophosphamide (BuCy) as the conditioning regimen in allogeneic hematopoietic stem cell transplantation (allo-HSCT) for acute myeloid leukemia (AML) in first complete remission (CR1). Methods Totally 108 AML-CR1 patients undergoing allo-HSCT were randomized into BuCy (busulfan 1.6 mg/kg, q12 hours, -7?~?-4d; cyclophosphamide 60 mg/kg.d, -3?~?-2d) or BuFlu (busulfan 1.6 mg/kg, q12 hours, -5?~?-2d; fludarabine 30 mg/m2.d, -6?~?-2d) group. Hematopoietic engraftment, regimen-related toxicity (RRT), graft-versus-host disease (GVHD), transplant related mortality (TRM), and overall survival were compared between the two groups. Results All patients achieved hematopoietic reconstitution except for two patients who died of RRT during conditioning. All patients obtained complete donor chimerism by day +30 post-transplantation. The incidence of total and III-IV RRT were 94.4% and 81.5% (P?=?0.038), and 16.7% and 0.0% (P?=?0.002), respectively, in BuCy and BuFlu group. With a median follow up of 609 (range, 3–2130) days after transplantation, the 5-year cumulative incidence of TRM were 18.8?±?6.9% and 9.9?±?6.3% (P?=?0.104); the 5-year cumulative incidence of leukemia relapse were 16.5?±?5.8% and 16.2?±?5.3% (P?=?0.943); the 5-year disease-free survival and overall survival were 67.4?±?7.6% and 75.3?±?7.2% (P = 0.315), and 72.3?±?7.5% and 81.9?±?7.0% (P?=?0.177), respectively in BuCy and BuFlu group. Conclusion Compared with BuCy, BuFlu as a myeloablative condition regimen was associated with lower toxicities and comparable anti-leukemic activity in AML-CR1 patients undergoing allo-HSCT.
机译:目的我们进行了一项前瞻性,随机,开放标签,多中心研究,比较了白消安加氟达拉滨(BuFlu)与白消安加环磷酰胺(BuCy)作为异基因造血干细胞移植(allo-HSCT)治疗急性髓性白血病(AML)的条件)的首批完全缓解(CR1)。方法将108例接受异基因造血干细胞移植的AML-CR1患者随机分为BuCy(环丙磺胺1.6 mg / kg,每12小时,-7?〜?-4d;环磷酰胺60 mg / kg.d,-3?〜?-2d)或BuFlu(环丁砜1.6 mg / kg,q12小时,-5?〜?-2d;氟达拉滨30 mg / m2.d,-6?〜?-2d)组。比较了两组的造血移植,方案相关毒性(RRT),移植物抗宿主病(GVHD),移植相关死亡率(TRM)和总生存期。结果除2例在治疗期间因RRT死亡的患者外,所有患者均实现了造血重建。移植后第30天,所有患者均获得完全的供体嵌合。在BuCy和BuFlu组中,总RRT和III-IV RRT的发生率分别为94.4%和81.5%(P?=?0.038),以及16.7%和0.0%(P?=?0.002)。移植后中位随访609天(范围3–2130天),TRM的5年累积发生率分别为18.8%±6.9%和9.9%±6.3%(P = 0.104)。白血病复发的5年累积发生率分别为16.5%±5.8%和16.2%±5.3%(P = 0.943)。 5年无病生存率和总生存率分别为67.4%±7.6%和75.3%±7.2%(P = 0.315),以及72.3%±7.5%和81.9%±7.0%(P ^ =? 0.177),分别位于BuCy和BuFlu组中。结论与BuCy相比,BuFlu作为一种清髓疗法,与接受同种HSCT的AML-CR1患者的毒性较低,抗白血病活性相当。

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