Weldon School of Biomedical Engineering, Purdue University, 206 South Martin Jischke Drive, West Lafayette, IN 47907, USA.
J Theor Biol. 2010 Jun 7;264(3):990-1002. doi: 10.1016/j.jtbi.2010.01.031. Epub 2010 Feb 4.
Acute lymphoblastic leukemia (ALL) is a common childhood cancer in which nearly one-quarter of patients experience a disease relapse. However, it has been shown that individualizing therapy for childhood ALL patients by adjusting doses based on the blood concentration of active drug metabolite could significantly improve treatment outcome. An adaptive model predictive control (MPC) strategy is presented in which maintenance therapy for childhood ALL is personalized using routine patient measurements of red blood cell mean corpuscular volume as a surrogate for the active drug metabolite concentration. A clinically relevant mathematical model is developed and used to describe the patient response to the chemotherapeutic drug 6-mercaptopurine, with some model parameters being patient-specific. During the course of treatment, the patient-specific parameters are adaptively identified using recurrent complete blood count measurements, which sufficiently constrain the patient parameter uncertainty to support customized adjustments of the drug dose. While this work represents only a first step toward a quantitative tool for clinical use, the simulated treatment results indicate that the proposed mathematical model and adaptive MPC approach could serve as valuable resources to the oncologist toward creating a personalized treatment strategy that is both safe and effective.
急性淋巴细胞白血病 (ALL) 是一种常见的儿童癌症,近四分之一的患者会经历疾病复发。然而,已经表明通过根据活性药物代谢物的血液浓度调整剂量来为儿童 ALL 患者个体化治疗,可以显著改善治疗结果。本文提出了一种自适应模型预测控制 (MPC) 策略,该策略使用红细胞平均体积作为活性药物代谢物浓度的替代物,对儿童 ALL 的维持治疗进行个性化处理。开发了一个临床相关的数学模型来描述化疗药物 6-巯基嘌呤对患者的反应,其中一些模型参数是患者特异性的。在治疗过程中,使用反复的全血细胞计数测量来自适应地识别患者特异性参数,这充分限制了患者参数不确定性,以支持药物剂量的定制调整。虽然这项工作只是朝着临床使用的定量工具迈出的第一步,但模拟治疗结果表明,所提出的数学模型和自适应 MPC 方法可以为肿瘤学家提供有价值的资源,以制定既安全又有效的个性化治疗策略。