Hospital Israelita Albert Einstein, São Paulo, Brazil.
Universidade Federal de São Paulo (UNIFESP), São Paulo, Brazil.
Hematol Oncol. 2020 Dec;38(5):773-781. doi: 10.1002/hon.2789. Epub 2020 Sep 28.
Busulfan is given in the conditioning regimens preceding hematopoietic stem cell transplantation (HSCT), and plasma levels can be monitored. A targeted, individualized systemic exposure (SE) dose can be achieved by calculating the area under the plasma concentration versus time curve (AUC). The objective of this study was to determine a cutoff value for safety for the AUC for busulfan plasma levels in patients undergoing HSCT. A total of 149 consecutive HSCT patients were studied. After an oral test dose of busulfan, we set target doses of 4000, 5000, or 6000 µMol⸱min/day, and analyzed the AUC of oral or intravenous Bu. These patients were compared with 53 historical control subjects who had received myeloablative conditioning regimen without busulfan pharmacokinetic monitoring. Using a test dose and the administration route had no impact on the sinusoidal obstructive syndrome (SOS) incidence, transplant-related mortality or 1-year overall survival. However, patients receiving busulfan at doses set up at AUC > 5000 had an increased risk to develop SOS after HSCT (hazard ratio 3.39, p = 0.034, 95% CI 1.09-10.52). Adjusting the busulfan dose according to SE levels target dose during conditioning is associated with lower rates of oral severe mucositis and SOS. A cutoff of 5000 µMol⸱min is safe and does not impair survival.
在进行造血干细胞移植 (HSCT) 之前,患者会接受白消安预处理方案,并且可以监测其血浆水平。通过计算血浆浓度-时间曲线下面积 (AUC),可以实现靶向、个体化的系统暴露 (SE) 剂量。本研究旨在确定白消安患者 HSCT 后其血浆水平 AUC 的安全截断值。共研究了 149 例连续 HSCT 患者。在口服白消安测试剂量后,我们设定了 4000、5000 或 6000µMol·min/天的目标剂量,并分析了口服或静脉内 Bu 的 AUC。将这些患者与 53 例未接受白消安药代动力学监测的接受清髓性预处理方案的历史对照患者进行比较。使用测试剂量和给药途径对窦阻塞综合征 (SOS) 发生率、移植相关死亡率或 1 年总生存率没有影响。然而,接受 AUC>5000 白消安剂量的患者在 HSCT 后发生 SOS 的风险增加 (风险比 3.39,p=0.034,95%CI 1.09-10.52)。根据 SE 水平调整预处理期间的白消安剂量目标与较低的口腔重度黏膜炎和 SOS 发生率相关。5000µMol·min 的截断值是安全的,不会影响生存。