Personalized Medicine for Colorectal and Breast Cancer

结直肠癌和乳腺癌的个性化医疗

基本信息

项目摘要

DESCRIPTION (provided by applicant): This Program Project Grant proposal addresses personalized medicine - health care targeting medical interventions to patients based on their individual characteristics, particularly their genetics. Our objective is to use an integrated, interdisciplinary approach to obtain evidence about key aspects of the translation of genomic information for breast and colorectal cancer into clinical practice and health policy. Our Program includes four Projects and two Cores with the Specific Aims to: Aim 1: Determine utilization of genomic risk stratification and targeted treatment by using the examples of gene expression profiling (GEP) and HER2/neu testing for trastuzumab (Herceptin(r)) for breast cancer. Aim 2: Develop an understanding of preferences for genomic testing and interventions using the example of Lynch-syndrome screening. Aim 3: Develop a generalized, flexible model for evaluating the cost-effectiveness of personalized medicine and estimate the cost-effectiveness of GEP, HER2/neu testing for trastuzumab, and Lynch syndrome screening using unique data from our Program Projects. Aim 4: Develop an evidence base for translating research findings into practice and policy by collecting and synthesizing data on the clinical applications and the regulatory, policy, and economic impacts of genetically based colorectal and breast cancer interventions. Aim 5: Provide Projects with resources for: conceptualizing, measuring, and investigating population differences; conducting qualitative and quantitative research; identifying and obtaining data sources; coordinating activities; and disseminating findings. The significance of this proposal lies in our goal to establish evidence-based information that will be useful to patients, clinicians, providers, researchers, and policymakers in assessing how personalized medicine can be most beneficial and efficient. Our results will have implications beyond the specific cancers studied, as the issues related to utilization, access, preferences, economics, value, and policy implications are relevant across cancer sites and interventions.
描述(由申请者提供):本计划项目资助提案旨在根据患者的个体特征,特别是他们的遗传特征,针对患者的医疗干预,提供个性化的医疗保健。我们的目标是使用一种综合的、跨学科的方法来获得关于乳腺癌和结直肠癌基因组信息转化为临床实践和卫生政策的关键方面的证据。我们的计划包括四个项目和两个核心,具体目标是: 目的1:以曲妥珠单抗(Herceptin(R))的基因表达谱(GEP)和HER2/neu检测为例,确定基因组风险分层和靶向治疗的应用。 目的2:以林奇综合征筛查为例,了解基因组检测和干预的偏好。 目的3:建立一个通用的、灵活的模型来评估个性化药物的成本-效果,并使用我们计划项目中的独特数据评估GEP、曲妥珠单抗的HER2/neu检测和Lynch综合征筛查的成本-效果。 目的4:通过收集和综合基于基因的结直肠癌和乳腺癌干预措施的临床应用以及监管、政策和经济影响的数据,为将研究成果转化为实践和政策建立证据基础。 目标5:为以下项目提供资源:概念化、衡量和调查人口差异;进行定性和定量研究;确定和获得数据来源;协调活动;传播调查结果。 这项建议的意义在于我们的目标是建立基于证据的信息,这些信息将对患者、临床医生、提供者、研究人员和政策制定者在评估个性化医疗如何最有益和最有效方面有用。我们的结果将具有超越所研究的特定癌症的影响,因为与利用、获取、偏好、经济、价值和政策影响相关的问题与癌症地点和干预措施相关。

项目成果

期刊论文数量(21)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Making genomic medicine evidence-based and patient-centered: a structured review and landscape analysis of comparative effectiveness research.
Value of Genetic Testing for Hereditary Colorectal Cancer in a Probability-Based US Online Sample.
基于概率的美国在线样本中,遗传性结直肠癌的基因检测值。
Capacity building for assessing new technologies: approaches to examining personalized medicine in practice.
  • DOI:
    10.2217/pme.10.36
  • 发表时间:
    2010-07
  • 期刊:
  • 影响因子:
    2.3
  • 作者:
    Van Bebber SL;Trosman JR;Liang SY;Wang G;Marshall DA;Knight S;Phillips KA
  • 通讯作者:
    Phillips KA
Using the coronary artery calcium score to guide statin therapy: a cost-effectiveness analysis.
  • DOI:
    10.1161/circoutcomes.113.000799
  • 发表时间:
    2014-03
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Pletcher MJ;Pignone M;Earnshaw S;McDade C;Phillips KA;Auer R;Zablotska L;Greenland P
  • 通讯作者:
    Greenland P
Closing the personalized medicine information gap: HER2 test documentation practice.
缩小个性化医疗信息差距:HER2 测试文档实践。
  • DOI:
  • 发表时间:
    2013
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Ferrusi,IliaL;Earle,CraigC;Trudeau,Maureen;Leighl,NatashaB;Pullenayegum,Eleanor;Khong,Hoa;Hoch,JeffreyS;Marshall,DeborahA
  • 通讯作者:
    Marshall,DeborahA
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KATHRYN A PHILLIPS其他文献

KATHRYN A PHILLIPS的其他文献

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{{ truncateString('KATHRYN A PHILLIPS', 18)}}的其他基金

BUILDING THE EVIDENCE BASE FOR APPROPRIATE AND EFFICIENT IMPLEMENTATION OF EMERGING GENOMIC TESTS FOR DISEASE MANAGEMENT AND SCREENING
为疾病管理和筛查的新兴基因组测试的适当和有效实施建立证据基础
  • 批准号:
    10227393
  • 财政年份:
    2021
  • 资助金额:
    $ 149.57万
  • 项目类别:
BUILDING THE EVIDENCE BASE FOR APPROPRIATE AND EFFICIENT IMPLEMENTATION OF EMERGING GENOMIC TESTS FOR DISEASE MANAGEMENT AND SCREENING
为疾病管理和筛查的新兴基因组测试的适当和有效实施建立证据基础
  • 批准号:
    10612889
  • 财政年份:
    2021
  • 资助金额:
    $ 149.57万
  • 项目类别:
BUILDING THE EVIDENCE BASE FOR APPROPRIATE AND EFFICIENT IMPLEMENTATION OF EMERGING GENOMIC TESTS FOR DISEASE MANAGEMENT AND SCREENING
为疾病管理和筛查的新兴基因组测试的适当和有效实施建立证据基础
  • 批准号:
    10447733
  • 财政年份:
    2021
  • 资助金额:
    $ 149.57万
  • 项目类别:
Coverage, Price, and Reimbursement for Multigene Tests for Cancer and Related Conditions
癌症及相关疾病多基因检测的承保范围、价格和报销
  • 批准号:
    10119135
  • 财政年份:
    2018
  • 资助金额:
    $ 149.57万
  • 项目类别:
Risk-Benefit Trade-Offs for Whole Genome Sequencing
全基因组测序的风险与收益权衡
  • 批准号:
    8899726
  • 财政年份:
    2013
  • 资助金额:
    $ 149.57万
  • 项目类别:
Risk-Benefit Trade-Offs for Whole Genome Sequencing
全基因组测序的风险与收益权衡
  • 批准号:
    8420250
  • 财政年份:
    2013
  • 资助金额:
    $ 149.57万
  • 项目类别:
Risk-Benefit Trade-Offs for Whole Genome Sequencing
全基因组测序的风险与收益权衡
  • 批准号:
    9010968
  • 财政年份:
    2013
  • 资助金额:
    $ 149.57万
  • 项目类别:
Risk-Benefit Trade-Offs for Whole Genome Sequencing
全基因组测序的风险与收益权衡
  • 批准号:
    8619652
  • 财政年份:
    2013
  • 资助金额:
    $ 149.57万
  • 项目类别:
Personalized Medicine for Colorectal and Breast Cancer
结直肠癌和乳腺癌的个性化医疗
  • 批准号:
    7687989
  • 财政年份:
    2008
  • 资助金额:
    $ 149.57万
  • 项目类别:
Screening for Colorectal Cancer: An Integrated Approach
结直肠癌筛查:综合方法
  • 批准号:
    6890430
  • 财政年份:
    2004
  • 资助金额:
    $ 149.57万
  • 项目类别:

相似国自然基金

Chinese Journal of Integrative Medicine
  • 批准号:
    81224004
  • 批准年份:
    2012
  • 资助金额:
    24.0 万元
  • 项目类别:
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Prediction of extrahepatic metastasis in colorectal cancer liver metastasis and application to Precision medicine
结直肠癌肝转移的肝外转移预测及其在精准医疗中的应用
  • 批准号:
    23K15475
  • 财政年份:
    2023
  • 资助金额:
    $ 149.57万
  • 项目类别:
    Grant-in-Aid for Early-Career Scientists
Establishment of tailor-made medicine for colorectal cancer arouse in serrated pathway
锯齿状通路激活结直肠癌定制药物的建立
  • 批准号:
    17K09476
  • 财政年份:
    2017
  • 资助金额:
    $ 149.57万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Personalised medicine markers of anti-EGFR antibody therapy in metastatic colorectal cancer: accelerating clinical translation with collaborative meta-analyses based on individual-participant data
转移性结直肠癌抗 EGFR 抗体治疗的个性化医学标志物:通过基于个体参与者数据的协作荟萃分析加速临床转化
  • 批准号:
    nhmrc : GNT1085364
  • 财政年份:
    2015
  • 资助金额:
    $ 149.57万
  • 项目类别:
    Project Grants
Personalised medicine markers of anti-EGFR antibody therapy in metastatic colorectal cancer: accelerating clinical translation with collaborative meta-analyses based on individual-participant data
转移性结直肠癌抗 EGFR 抗体治疗的个性化医学标志物:通过基于个体参与者数据的协作荟萃分析加速临床转化
  • 批准号:
    nhmrc : 1085364
  • 财政年份:
    2015
  • 资助金额:
    $ 149.57万
  • 项目类别:
    Project Grants
Methods for the economic evaluation of personalized medicine: a case study in advanced colorectal cancer
个性化医疗的经济评估方法:晚期结直肠癌的案例研究
  • 批准号:
    327830
  • 财政年份:
    2014
  • 资助金额:
    $ 149.57万
  • 项目类别:
    Studentship Programs
Translating gene-calcium interactions to precision medicine for colorectal cancer
将基因-钙相互作用转化为结直肠癌的精准医学
  • 批准号:
    9003793
  • 财政年份:
    2014
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    $ 149.57万
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Translating gene-calcium interactions to precision medicine for colorectal cancer
将基因-钙相互作用转化为结直肠癌的精准医学
  • 批准号:
    8624955
  • 财政年份:
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    $ 149.57万
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Translating gene-calcium interactions to precision medicine for colorectal cancer
将基因-钙相互作用转化为结直肠癌的精准医学
  • 批准号:
    8803375
  • 财政年份:
    2014
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    $ 149.57万
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Improving compliance with colorectal cancer screening in family medicine residenc
提高家庭住院医师结直肠癌筛查的依从性
  • 批准号:
    7429286
  • 财政年份:
    2008
  • 资助金额:
    $ 149.57万
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Improving compliance with colorectal cancer screening in family medicine residenc
提高家庭住院医师结直肠癌筛查的依从性
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    8132459
  • 财政年份:
    2008
  • 资助金额:
    $ 149.57万
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