van Hoogdalem Matthijs W, Emoto Chie, Fukuda Tsuyoshi, Mizuno Tomoyuki, Mehta Parinda A, Vinks Alexander A
Division of Clinical Pharmacology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
Br J Clin Pharmacol. 2020 May;86(5):933-943. doi: 10.1111/bcp.14202. Epub 2020 Jan 23.
Fanconi anaemia (FA) is a rare disorder characterized by progressive bone marrow failure that requires haematopoietic cell transplantation (HCT). Busulfan is used in conditioning regimens prior to HCT. Doses used in non-FA patients cause life-threatening toxicities in FA patients and data on busulfan pharmacokinetics (PK) in this population are limited. This study characterized busulfan PK in paediatric FA patients using population PK modelling and evaluated the effect of body composition on steady-state concentrations (C ).
A total of 200 busulfan plasma concentrations in 29 FA patients from a recent study (Clinicaltrials.gov; NCT01082133) were available for population PK modelling. The effect of different body size-scaled doses and body compositions on C was investigated using population PK modelling.
Fat free mass (FFM) was identified as the best size descriptor in a two-compartment busulfan PK model in FA patients. Conventional dosing, based on an amount of busulfan per kilogram of total body mass, resulted in higher C in FA patients with higher body mass index (BMI). A newly proposed FFM-based dosing strategy would eliminate the observed trend of higher concentrations in high BMI patients, and achieve consistent C across a wide BMI spectrum.
This is the first study to describe the population PK of busulfan in paediatric FA patients. The proposed model will facilitate PK model-informed precision dosing. FFM-based dosing is expected to improve the probability of achieving target C , particularly in obese patients, while minimizing the risk of overdosing.
范可尼贫血(FA)是一种罕见的疾病,其特征为进行性骨髓衰竭,需要进行造血细胞移植(HCT)。白消安用于HCT前的预处理方案。非FA患者使用的剂量在FA患者中会导致危及生命的毒性,且该人群中白消安药代动力学(PK)的数据有限。本研究采用群体PK建模对儿科FA患者的白消安PK进行了特征描述,并评估了身体组成对稳态浓度(C)的影响。
从最近一项研究(Clinicaltrials.gov;NCT01082133)的29例FA患者中获得了总共200份白消安血浆浓度,用于群体PK建模。使用群体PK建模研究了不同体重标化剂量和身体组成对C的影响。
在FA患者的二室白消安PK模型中,去脂体重(FFM)被确定为最佳的大小描述指标。基于每千克总体重的白消安用量的传统给药方法,导致体重指数(BMI)较高的FA患者的C更高。一种新提出的基于FFM的给药策略将消除在高BMI患者中观察到的较高浓度趋势,并在广泛的BMI范围内实现一致的C。
这是第一项描述儿科FA患者白消安群体PK的研究。所提出的模型将有助于基于PK模型的精准给药。预计基于FFM的给药将提高达到目标C的概率,特别是在肥胖患者中,同时将过量用药的风险降至最低。