Bleyzac N, Souillet G, Magron P, Janoly A, Martin P, Bertrand Y, Galambrun C, Dai Q, Maire P, Jelliffe R W, Aulagner G
Department of Pharmacy, Debrousse Hospital, Lyon, France.
Bone Marrow Transplant. 2001 Oct;28(8):743-51. doi: 10.1038/sj.bmt.1703207.
In order to control busulfan pharmacokinetic variability and toxicity, a specific monitoring protocol was instituted in our bone marrow transplant BMT paediatric patients including a test dose, daily Bayesian forecasting of busulfan plasma levels, and Bayesian individualization of busulfan dosage regimens. Twenty-nine children received BMT after a busulfan-based conditioning regimen. Individual pharmacokinetic parameters were obtained following a 0.5 mgkg test dose and were used for daily individualization of dosage regimens during the subsequent 4-day course of treatment. Doses were adjusted to reach a target mean AUC per 6 h between 4 and 6 microg.h.ml(+1). Plasma busulfan assays were performed by liquid chromatography. Pharmacokinetic analysis used the USCPACK software. The performance of the test dose to predict AUC during the busulfan regimen was evaluated. Incidence of toxicity, chimerism and relapse, overall Kaplan-Meier survival, and VOD-free survival were compared after matching our patients (group A) with patients conditioned by using standard doses of busulfan (group B). Busulfan doses were decreased in 69% of patients compared to conventional doses. Expected AUC was significantly correlated with observed AUC and predictability of the test dose was 101.9 +/- 17.9%. Incidence of VOD in group A was 3.4% vs 24.1% in group B, while the incidence of stomatitis was similar. Engraftment was successful in all patients in group A. The rate of full engraftment at 3 months post-BMT was higher in group A (P = 0.012). Long-term overall survival did not differ between the two groups, in contrast to the 90-day survival. VOD-free survival was higher in group A (P = 0.026). Pharmacokinetic monitoring and individualization of busulfan dosage regimen are useful in improving clinical outcome and reducing early mortality in paediatric bone marrow transplant recipients.
为了控制白消安的药代动力学变异性和毒性,我们为接受骨髓移植(BMT)的儿科患者制定了一项特定的监测方案,包括一次试验剂量、白消安血浆水平的每日贝叶斯预测以及白消安给药方案的贝叶斯个体化。29名儿童在接受基于白消安的预处理方案后接受了BMT。在给予0.5mg·kg的试验剂量后获得个体药代动力学参数,并在随后4天的治疗过程中用于每日给药方案的个体化。调整剂量以使每6小时的目标平均AUC达到4至6μg·h·ml(+1)。通过液相色谱法进行血浆白消安测定。药代动力学分析使用USC*PACK软件。评估了试验剂量在白消安给药方案期间预测AUC的性能。在将我们的患者(A组)与使用标准剂量白消安进行预处理的患者(B组)进行匹配后,比较了毒性、嵌合率和复发率、总体Kaplan-Meier生存率以及无肝静脉闭塞病(VOD)生存率。与传统剂量相比,69%的患者白消安剂量降低。预期AUC与观察到的AUC显著相关,试验剂量的预测性为101.9±17.9%。A组VOD的发生率为3.4%,而B组为24.1%,而口腔炎的发生率相似。A组所有患者移植均成功。BMT后3个月时A组的完全植入率更高(P = 0.012)。与90天生存率不同,两组的长期总生存率没有差异。A组的无VOD生存率更高(P = 0.026)。白消安给药方案的药代动力学监测和个体化有助于改善儿科骨髓移植受者的临床结局并降低早期死亡率。