Division of Hematology, Saitama Medical Center, Jichi Medical University, Saitama, Japan.
Division of Hematology, Department of Medicine, Jichi Medical University, Shimotsuke, Japan.
Biol Blood Marrow Transplant. 2018 Oct;24(10):2139-2144. doi: 10.1016/j.bbmt.2018.04.015. Epub 2018 Apr 19.
Compared with 4-times-daily infusion of intravenous busulfan (ivBU4), the safety and efficacy of once-daily infusion of ivBU (ivBU1) has not been fully clarified. We have been routinely using ivBU1 in a conditioning regimen in adult patients with myeloid malignancy who undergo allogeneic hematopoietic stem cell transplantation. In this study, a total of 91 patients who received ivBU1 for 2 days (n = 18) or 4 days (n = 73) in our institutions were compared with 273 control patients who received ivBU4, who were matched for age, sex, performance status, disease risk, conditioning regimen, and donor type, selected from the database of the Japanese Society for Hematopoietic Cell Transplantation using optimal matching algorithms. One-year overall survival (56.8% versus 57.1%, P = .94), disease-free survival (51.6% versus 50.8%, P = .73), relapse rate (28.5% versus 26.2%, P = .94), nonrelapse mortality (19.9% versus 23.0%, P = .71), and the incidence of graft-versus-host disease were not significantly different between the ivBU1 and ivBU4 groups. In patients who received ivBU1, neutrophil recovery was slower (median days: 22 versus 17, P = .001), and the incidence of veno-occlusive disease was lower (2.6% versus 17.4%, P = .04). In conclusion, ivBU1 can be safely administered with clinical outcomes similar to those with ivBU4.
与静脉注射白消安(ivBU4)每日 4 次输注相比,每日 1 次输注 ivBU(ivBU1)的安全性和疗效尚未完全阐明。我们一直在常规使用 ivBU1 作为接受异基因造血干细胞移植的髓系恶性肿瘤成人患者的预处理方案。在这项研究中,我们比较了在我院接受 ivBU1 2 天(n = 18)或 4 天(n = 73)的 91 例患者与接受 ivBU4 的 273 例对照患者,后者通过最佳匹配算法从日本血液和骨髓移植学会的数据库中选择,在年龄、性别、表现状态、疾病风险、预处理方案和供体类型方面与 ivBU1 组相匹配。两组患者的 1 年总生存率(56.8%与 57.1%,P = .94)、无病生存率(51.6%与 50.8%,P = .73)、复发率(28.5%与 26.2%,P = .94)、非复发死亡率(19.9%与 23.0%,P = .71)和移植物抗宿主病发生率均无显著差异。接受 ivBU1 的患者中性粒细胞恢复较慢(中位数天数:22 与 17,P = .001),静脉闭塞性疾病发生率较低(2.6%与 17.4%,P = .04)。总之,ivBU1 可安全给药,其临床结局与 ivBU4 相似。