McMichael J, Lieberman R, Doyle H, McCauley J, Fung J, Starzl T E
Transplantation Institute, University of Pittsburgh, PA 15213.
J Clin Pharmacol. 1993 Jul;33(7):599-605. doi: 10.1002/j.1552-4604.1993.tb04711.x.
The accuracy and precision of an intelligent dosing system (IDS) for FK506 in predicting doses to achieve target drug levels has been prospectively evaluated in transplant and autoimmune patients. For dose individualization, the knowledge base is updated with patient-specific feedback including the current dose, drug level, and the new target level. The study population of 147 patients consisted of 97 transplant patients (liver and kidney) and 50 patients with autoimmune disorders. Patients in the transplant study group were entered sequentially and followed as a cohort. Patients in the autoimmune study group were randomly assigned to one of three predefined FK506 concentration windows (low, 0.1-.3; medium, 0.4-.7; and high, 0.8-1.3 ng/mL) as part of a concentration controlled clinical trial. Predictions of steady-state plasma drug levels were made throughout the clinical course of autoimmune patients and during the first 6 weeks post-transplant in liver and kidney recipients. FK506 concentration in plasma was measured by a monoclonal antibody based ELISA assay. Accuracy was computed as the mean prediction error (mpe). Precision was computed as the root mean squared prediction error (rmspe). The accuracy of the IDS in each study group was as follows: 0.016 ng/mL (liver), -0.034 ng/mL (kidney), and -0.022 ng/mL (autoimmune). Because the 95% confidence interval included zero in each case, the IDS showed no bias. The precision of the IDS in each study group was as follows: 0.133 ng mL (liver), 0.1903 ng/mL (kidney), and 0.1188 ng/mL (autoimmune). These results indicate that the FK506 IDS is both accurate and very precise (reproducible) in transplant and autoimmune patients.(ABSTRACT TRUNCATED AT 250 WORDS)
在移植患者和自身免疫性疾病患者中,前瞻性评估了一种用于预测实现目标药物水平所需剂量的FK506智能给药系统(IDS)的准确性和精密度。为了实现剂量个体化,根据患者特定的反馈(包括当前剂量、药物水平和新的目标水平)更新知识库。147例患者的研究群体包括97例移植患者(肝脏和肾脏移植)和50例自身免疫性疾病患者。移植研究组的患者按顺序入组并作为一个队列进行随访。作为浓度控制临床试验的一部分,自身免疫性研究组的患者被随机分配到三个预定义的FK506浓度窗口之一(低浓度,0.1 - 0.3;中等浓度,0.4 - 0.7;高浓度,0.8 - 1.3 ng/mL)。在自身免疫性疾病患者的整个临床过程以及肝脏和肾脏移植受者移植后的前6周内,对稳态血浆药物水平进行预测。通过基于单克隆抗体的ELISA测定法测量血浆中的FK506浓度。准确性计算为平均预测误差(mpe)。精密度计算为均方根预测误差(rmspe)。每个研究组中IDS的准确性如下:0.016 ng/mL(肝脏)、 - 0.034 ng/mL(肾脏)和 - 0.022 ng/mL(自身免疫性疾病)。由于每种情况下95%置信区间都包含零,因此IDS无偏差。每个研究组中IDS的精密度如下:0.133 ng/mL(肝脏)、0.1903 ng/mL(肾脏)和0.1188 ng/mL(自身免疫性疾病)。这些结果表明,FK506 IDS在移植患者和自身免疫性疾病患者中既准确又非常精密(可重复)。(摘要截断于250字)