a Division of Hematology/Medical Oncology , Mayo Clinic , Phoenix , AZ , USA.
b Division of Biostatistics , Mayo Clinic , Phoenix , AZ , USA.
Leuk Lymphoma. 2019 Aug;60(8):2034-2041. doi: 10.1080/10428194.2018.1562183. Epub 2019 Jan 10.
Therapeutic dose monitoring is widely adopted for determination of busulfan (Bu) dose for use as a conditioning regimen. However, while dose adjustments are being incorporated, transient fluctuations of Bu levels may occur. We aim to understand if these fluctuations affect clinical outcomes of these patients. We compared outcomes in patients in whom the absolute dose changes and fluctuation of AUC were ≥ median% versus < median%. Rates of sinusoidal obstructive syndrome, grades 2-4/grades 3-4 acute and chronic graft versus host disease were not different between the two cohorts. The Kaplan-Meier curves for overall survival showed no significant differences. Six patients required >50% dose adjustment and four had a fluctuation in AUC of >50%. One of these patients died of sinusoidal obstruction syndrome and two died of infections. In our study, the transient fluctuations in Bu levels did not affect clinical outcomes; hence obviating the need for test dose strategy.
治疗剂量监测被广泛用于确定白消安(Bu)剂量作为预处理方案。然而,在进行剂量调整时,Bu 水平可能会出现短暂波动。我们旨在了解这些波动是否会影响这些患者的临床结果。我们比较了绝对剂量变化和 AUC 波动≥中位数%与<中位数%的患者的结果。两组患者的窦状阻塞综合征、2-4 级/3-4 级急性和慢性移植物抗宿主病的发生率无差异。总体生存的 Kaplan-Meier 曲线没有显示出显著差异。6 名患者需要调整>50%的剂量,4 名患者的 AUC 波动>50%。其中一名患者死于窦状阻塞综合征,两名患者死于感染。在我们的研究中,Bu 水平的短暂波动并未影响临床结果;因此无需采用测试剂量策略。