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Lung Cancer Model: Risk, Progression and Intervention

Lung Cancer Model: Risk, Progression and Intervention
肺癌模型:风险、进展和干预
批准号:
7681603
负责人:
MAREK KIMMEL
金额:
$22.08万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-09-18 至 2012-08-31

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中文摘要
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英文摘要
DESCRIPTION (provided by applicant): In the course of previous CISNET funding period, we developed two complementary models of lung cancer: (i) Model of carcinogenesis, extended to include genetic susceptibility and impact of smoking pattern, (ii) Model of progression, detection and treatment, based on stochastic tumor growth and stochastic stage transitions. The main trust of the research planned will be focused on two Aims: Aim 1. To determine population impact of interventions such as: (a) Smoking cessation and prevention of initiation, (b) Early detection of lung cancer by periodic screening using helical CT, in a high-risk population, followed by therapy, (c) Lifestyle interventions (e.g., dietary), removal of exposures (ETS, asbestos, radon). Aim 2. Predict the population impact of novel interventions, not yet developed, such as genetic screening of heavy smokers and other high-risk groups, detection using new biomarkers, new treatment modalities and so forth..While the impact of smoking on lung cancer is generally well understood, there are certain aspects of this modeling which are still a major challenge, e.g., gaining a better understanding of the process of carcinogenesis for those who have quit smoking and understanding trends in lung cancer among nonsmokers. This implies our Aim 3. To model carcinogenesis and natural history of lung cancer in former smokers and never smokers. Modeling is the only method that allows extrapolation of results of controlled cancer intervention studies to estimates of US population and community effectiveness. Current models, as it is seen from the review above, do not address existing inter-individual variability in susceptibility, natural history, response to treatment, and so forth. The individual-based approach to modeling, which we are taking in this application, will allow addressing this variability. The individual-based approach is also suitable for modeling of interventions, which do not yet exist such as new treatments.
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DOI: 10.1186/1471-2288-11-64
发表时间: 2011-05-11
期刊: BMC medical research methodology
影响因子: 4
作者: [Foy M, Chen X, Kimmel M, Gorlova OY]
通讯作者: Gorlova OY
Collaborative Research : Stochastic Modeling and Estimation of Gene Transcription
  • 批准号:
    8053024
  • 项目类别:
  • 资助金额:
    $19.14万
  • 财政年份:
    2010
  • 负责人:
    MAREK KIMMEL
  • 依托单位:
Collaborative Research : Stochastic Modeling and Estimation of Gene Transcription
  • 批准号:
    7667461
  • 项目类别:
  • 资助金额:
    $36.83万
  • 财政年份:
    2008
  • 负责人:
    MAREK KIMMEL
  • 依托单位:
Collaborative Research : Stochastic Modeling and Estimation of Gene Transcription
  • 批准号:
    8099694
  • 项目类别:
  • 资助金额:
    $36.16万
  • 财政年份:
    2008
  • 负责人:
    MAREK KIMMEL
  • 依托单位:
Collaborative Research : Stochastic Modeling and Estimation of Gene Transcription
  • 批准号:
    7884326
  • 项目类别:
  • 资助金额:
    $36.52万
  • 财政年份:
    2008
  • 负责人:
    MAREK KIMMEL
  • 依托单位:
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