Integrated PK-PD and agent-based modeling in oncology

被引:56
作者
Wang, Zhihui [1 ]
Butner, Joseph D. [2 ,3 ]
Cristini, Vittorio [1 ,2 ,3 ,4 ]
Deisboeck, Thomas S. [5 ,6 ]
机构
[1] Univ New Mexico, Dept Pathol, Albuquerque, NM 87131 USA
[2] Univ New Mexico, Dept Chem Engn, Albuquerque, NM 87131 USA
[3] Univ New Mexico, Ctr Biomed Engn, Albuquerque, NM 87131 USA
[4] King Abdulaziz Univ, Dept Math, Fac Sci, Jeddah 21589, Saudi Arabia
[5] Massachusetts Gen Hosp, Dept Radiol, Charlestown, MA 02129 USA
[6] Harvard Univ, Sch Med, Charlestown, MA 02129 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
Chemotherapy; Computer simulation; Mathematical modeling; Multiscale; Tumor growth and invasion; Translational research; CELL LUNG-CANCER; NONLINEAR TUMOR-GROWTH; CARCINOMA IN-SITU; BREAST-CANCER; INTERSTITIAL PRESSURE; SENSITIVITY-ANALYSIS; ANTITUMOR-ACTIVITY; AUTOMATON MODEL; DRUG RESPONSE; CROSS-SCALE;
D O I
10.1007/s10928-015-9403-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Mathematical modeling has become a valuable tool that strives to complement conventional biomedical research modalities in order to predict experimental outcome, generate new medical hypotheses, and optimize clinical therapies. Two specific approaches, pharmacokinetic-pharmacodynamic (PK-PD) modeling, and agent-based modeling (ABM), have been widely applied in cancer research. While they have made important contributions on their own (e.g., PK-PD in examining chemotherapy drug efficacy and resistance, and ABM in describing and predicting tumor growth and metastasis), only a few groups have started to combine both approaches together in an effort to gain more insights into the details of drug dynamics and the resulting impact on tumor growth. In this review, we focus our discussion on some of the most recent modeling studies building on a combined PK-PD and ABM approach that have generated experimentally testable hypotheses. Some future directions are also discussed.
引用
收藏
页码:179 / 189
页数:11
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