Modeling NSCLC Progression: Recent Advances and Opportunities Available

被引:12
|
作者
Suleiman, Ahmed Abbas [1 ]
Nogova, Lucia [2 ]
Fuhr, Uwe [1 ]
机构
[1] Univ Hosp Cologne, Dept Pharmacol, D-50931 Cologne, Germany
[2] Univ Hosp Cologne, Lung Canc Grp Cologne, Dept Internal Med 1, Ctr Integrated Oncol, D-50931 Cologne, Germany
来源
AAPS JOURNAL | 2013年 / 15卷 / 02期
关键词
disease progression; drug development; lung cancer; modeling; tumor growth; CELL LUNG-CANCER; CLINICAL DRUG DEVELOPMENT; POSITRON-EMISSION-TOMOGRAPHY; PHASE-II; TUMOR-GROWTH; PHARMACODYNAMIC MODEL; DISEASE PROGRESSION; ANTICANCER AGENTS; RANDOMIZED-TRIAL; EARLY PREDICTION;
D O I
10.1208/s12248-013-9461-y
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Non-small cell lung cancer (NSCLC) is one of the leading causes of death around the world with an estimated 5-year relative survival rate of 16% at diagnosis. Development of drugs treating NSCLC is not easy, and the success rate for an anticancer treatment to pass through the whole clinical development process is as low as 5%. Modeling and simulation lend themselves as tools which can potentially streamline drug development. A critical component of the models developed is a description of how the disease progresses over time and how a treatment would affect its trajectory. Our aim was to review the literature to present the models and growth functions which have been used for describing NSCLC dynamics, and how anticancer treatments can affect such dynamics, both in animals and in humans. Only a limited set of models were identified for such a purpose. Most of the models which have been used were descriptive of tumor growth, yet there were attempts to account for the underlying processes, especially in animals where it is more feasible to collect data needed for developing such models. Moreover, we discuss how modeling and simulation can aid in decision making across the different stages of drug development. Based on some encouraging results from trials of other cancer types where modeling tumor dynamics has played an important role, we propose further exploration of NSCLC using model-based techniques and further use of these techniques in designing and evaluating NSCLC trials.
引用
收藏
页码:542 / 550
页数:9
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