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The main goal of our proposed research is to quantify the impact of screeningand treatment interventionson breast cancer incidenceand mortality trends in the United States through a collaborative research agreement with the NCIs Cancer Intervention and Surveillance Modeling Network (CISNET). Under our original CISNET award, we quantified the relativecontributionsof screening mammography and multiagent chemotherapy to the recent decline in breast cancer mortality. In this application, we are proposing to extend our analysis of the current breast cancer trends to include the impact of screen-detected DCIS. We will also identify the component of current trends in breast cancer incidence and mortality attributableto the subpopulation at high genetic risk for developingthe disease. In additionto studying the current trends more closely, we will extend the use of our model to the study of future trends. Through a CISNET/DHHS supplemental award, we have already performed a pilot study on the use of our model in determining whether or not the Healthy People 2010 goals in breast cancer mortalitycould be achieved. This project revealed the need to enhance our existing CISNET model so that it could take as inputs intermediate endpointsfrom screening and treatment trials. More often than not the performance of medical innovations are being evaluated on short term endpoints or surrogate markers. New treatment protocols are now being broadly adopted on the basis of lowered recurrence rates, with little knowledge of their impact on survival. New screening technologies are being advocated on the basis of increased detection rates, with little knowledgeof their impact on survival. We want to extrapolate the intermediate endpoints of breast cancer trials in screening and treatment to long term survival endpoints and then translate these findings to the population level. We will focus a part of our efforts on the study of new screening technologies in the high risk population in order to better understand how these interventions can be translated to the general population.We will make our CISNET model availablefor broader publicconsumption and welcome pressing questions from policy makers during the course of our study.
期刊论文(5)
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会议论文
DOI: 10.1007/s10552-011-9866-9
发表时间: 2012-01
期刊: CANCER CAUSES & CONTROL
影响因子: 2.3
作者: [Lin, Ray S., Plevritis, Sylvia K.]
通讯作者: Plevritis, Sylvia K.
DOI: 10.1093/jncimonographs/lgj012
发表时间: 2006-01-01
期刊: Journal of the National Cancer Institute. Monographs
影响因子: --
作者: [Plevritis, Sylvia K, Sigal, Bronislava M, Glynn, Peter]
通讯作者: Glynn, Peter
DOI: 10.1158/1055-9965.epi-12-0149
发表时间: 2012-07
期刊: Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology
影响因子: --
作者: [Sigal BM, Munoz DF, Kurian AW, Plevritis SK]
通讯作者: Plevritis SK
DOI: 10.1158/0008-5472.can-13-0759
发表时间: 2014-01-15
期刊: Cancer research
影响因子: 11.2
作者: [Gallaher J, Babu A, Plevritis S, Anderson ARA]
通讯作者: Anderson ARA
Project 2 Human Tumor Analysis
  • 批准号:
    10729467
  • 项目类别:
  • 资助金额:
    $52.27万
  • 财政年份:
    2023
  • 负责人:
    SYLVIA KATINA PLEVRITIS
  • 依托单位:
Administrative Core
  • 批准号:
    10729465
  • 项目类别:
  • 资助金额:
    $36.05万
  • 财政年份:
    2023
  • 负责人:
    SYLVIA KATINA PLEVRITIS
  • 依托单位:
Data Analysis Core
  • 批准号:
    10531082
  • 项目类别:
  • 资助金额:
    $43.55万
  • 财政年份:
    2022
  • 负责人:
    SYLVIA KATINA PLEVRITIS
  • 依托单位:
Data Analysis Core
  • 批准号:
    10709577
  • 项目类别:
  • 资助金额:
    $52.33万
  • 财政年份:
    2022
  • 负责人:
    SYLVIA KATINA PLEVRITIS
  • 依托单位:
海外基金