Department of Hematology, Japanese Red Cross Nagoya First Hospital, Japan.
Cancer Sci. 2012 Sep;103(9):1688-94. doi: 10.1111/j.1349-7006.2012.02342.x. Epub 2012 Jul 16.
We aimed to evaluate the efficacy and safety of allogeneic hematopoietic stem cell transplantation with targeted oral busulfan (BU) and cyclophosphamide (CY) in a phase II study. Busulfan (1.0 mg/kg) was given initially in six doses. Based on the estimated concentration at steady state after the first dose of BU, subsequent (7th-16th) doses were adjusted to obtain a targeted overall concentration at steady state of 700-900 ng/mL. The primary endpoint was 1-year overall survival (OS). Fifty patients were registered and 46 (median age, 53 years; range, 18-62 years) received planned transplant, including 24 with AML, 16 with myelodysplastic syndrome, and six with CML. Fourteen patients were categorized as standard risk. Nineteen patients received transplant from human leukocyte antigen-identical siblings, 27 from unrelated donors. The BU dose required reduction in 32 patients and escalation in six patients. One-year OS was 65% (95% confidence interval, 50-77%). Cumulative incidence of hepatic sinusoidal obstruction syndrome was 11%. One-year transplant-related mortality was 18%. Both OS and transplant-related mortality were favorable in this study, including patients of older age and with high risk diseases. Individual dose adjustment based on BU pharmacokinetics was feasible and effective in the current phase II study. This trial is registered in the University Hospital Medical Information Network Clinical Trial Registry System (UMIN-CTR, ID:C000000156).
我们旨在评估异体造血干细胞移植联合靶向口服白消安(BU)和环磷酰胺(CY)在 II 期研究中的疗效和安全性。BU 初始给予 1.0mg/kg,分 6 次给予。根据首次 BU 给药后稳态时的估计浓度,调整后续(第 7-16 次)剂量,以获得稳态时目标总浓度 700-900ng/ml。主要终点为 1 年总生存率(OS)。共登记了 50 例患者,其中 46 例(中位年龄 53 岁;范围 18-62 岁)接受了计划中的移植,包括 24 例急性髓系白血病、16 例骨髓增生异常综合征和 6 例慢性髓系白血病。14 例患者被归类为标准风险。19 例患者接受 HLA 完全匹配的同胞供者移植,27 例接受无关供者移植。32 例患者需要减少 BU 剂量,6 例患者需要增加 BU 剂量。1 年 OS 为 65%(95%置信区间,50-77%)。肝脏窦状隙阻塞综合征的累积发生率为 11%。1 年移植相关死亡率为 18%。包括年龄较大和患有高危疾病的患者在内,本研究的 OS 和移植相关死亡率均较好。基于 BU 药代动力学的个体化剂量调整在本 II 期研究中是可行且有效的。该试验在日本临床试验注册中心(UMIN-CTR)注册(注册号:C000000156)。