Great Lakes New England Clinical Validation Center

新英格兰五大湖临床验证中心

基本信息

项目摘要

The Great Lakes New England Clinical Validation Center (GLNE CVC), a Clinical Validation Consortium component of the Early Detection Research Network (EDRN) is a highly collaborative group of investigators whose aims to validate biomarkers for the early detection and risk assessment of cancers of the gastrointestinal tract. In this fifth competitive application, the GLNE continues to test the overall hypothesis that a panel of circulating and stool based biomarkers will increase the adherence to colorectal screening and in doing so reduce mortality caused by colorectal cancers. Based on the rising incidence of colorectal cancer (CRC) among adults age <50 in the US, and the low compliance and high mortality in underserved populations, increased emphasis is placed on these populations. The GLNE also proposes to continue its ongoing support of EDRN discovery priorities. We propose to address the following aims: (1) Primary Aim To expand and renew the archive of appropriately preserved stool, serum, plasma, urine, tissue and DNA biospecimens to be used by EDRN investigators for current and future validation and biomarker discovery research with expanded inclusion of subjects with early-onset CRC and underserved populations. This will allow assessment of the utility of individual stool-based, and serum-based biomarkers and biomarker panels for discriminating between individuals without neoplasia (subjects both at average and higher risk for developing colon cancer), and those with colon cancer or screen-relevant neoplasia (cancer plus advanced adenoma), and construction of panels of markers to discriminate between these groups. (2) To perform validation trials of promising biomarkers discovered by EDRN investigators, external collaborating institutions and collaborating EDRN industrial partners for the early detection of colorectal neoplasia. In this context we propose to (a) to clinically validate (via a methods comparison study) the performance of a point-of-care blood- based biomarker panel with the testing of serum/plasma samples obtained in clinics serving low-income and underserved communities and (b) to clinically validate an established 4-plex stool protein panel for early diagnosis of CRC. (3) To follow prospectively subjects enrolled in an established prospective Phase 2 validation trial to identify pre-diagnostic specimens which may be used to develop predictive markers.
五大湖新英格兰临床验证中心(GLNE CVC),临床验证联盟 早期发现研究网络(EDRN)的一个组成部分是一个高度合作的研究小组 其目的是验证用于胃肠道癌症早期检测和风险评估的生物标志物, 道。在这第五个竞争性应用程序中,GLNE继续测试整体假设, 基于循环和粪便的生物标志物将增加对结肠直肠筛查的依从性, 结直肠癌导致的死亡率。基于成年人结直肠癌(CRC)发病率的上升, 在美国,年龄<50岁,以及服务不足人群的低依从性和高死亡率, 都是针对这些人的GLNE还建议继续支持EDRN发现 优先事项我们建议实现以下目标:(1)主要目标 EDRN使用的适当保存的粪便、血清、血浆、尿液、组织和DNA生物标本 研究人员对当前和未来的验证和生物标志物发现研究进行了扩展, 早发CRC受试者和服务不足人群。这将有助于评估个人的效用。 基于粪便和基于血清的生物标志物和生物标志物组,用于区分个体, 肿瘤(处于结肠癌平均风险和较高风险的受试者)和结肠癌患者 或筛查相关瘤形成(癌症加晚期腺瘤),以及构建标记物组, 区别对待这些群体。(2)对EDRN发现的有前景的生物标志物进行验证试验 研究人员、外部合作机构和EDRN工业合作伙伴,以进行早期检测 结直肠肿瘤在这种情况下,我们建议(a)进行临床验证(通过方法比较研究) 基于血液的即时生物标志物面板在检测血清/血浆样本时的性能 在服务于低收入和服务不足社区的诊所中获得,以及(B)临床验证已建立的 4-复合粪便蛋白检测对结直肠癌早期诊断的价值(3)前瞻性随访入组的受试者, 已建立的前瞻性II期验证试验,以确定可用于 开发预测标记。

项目成果

期刊论文数量(27)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Detection of mutated K-ras DNA in urine, plasma, and serum of patients with colorectal carcinoma or adenomatous polyps.
Detecting K-ras mutations in stool from fecal occult blood test cards in multiphasic screening for colorectal cancer.
  • DOI:
    10.1016/j.canlet.2007.01.023
  • 发表时间:
    2007-08
  • 期刊:
  • 影响因子:
    9.7
  • 作者:
    G. Rennert;D. Kislitsin;D. Brenner;H. Rennert;Z. Lev
  • 通讯作者:
    G. Rennert;D. Kislitsin;D. Brenner;H. Rennert;Z. Lev
Screening for cancer with molecular markers: progress comes with potential problems.
  • DOI:
    10.1038/nrc3260
  • 发表时间:
    2012-04-12
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
Detection of a K-ras mutation in urine of patients with colorectal cancer.
结直肠癌患者尿液中 K-ras 突变的检测。
Fecal DNA-Based Detection of Colorectal Neoplasia.
基于粪便 DNA 的结直肠肿瘤检测。
  • DOI:
    10.1007/s11888-007-0027-1
  • 发表时间:
    2007
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Turgeon,DKim;Brenner,DeanE
  • 通讯作者:
    Brenner,DeanE
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ROBERT S BRESALIER其他文献

ROBERT S BRESALIER的其他文献

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{{ truncateString('ROBERT S BRESALIER', 18)}}的其他基金

Multi-cancer early detection using cell-free DNA methylome analysis
使用游离 DNA 甲基化分析进行多癌症早期检测
  • 批准号:
    10763305
  • 财政年份:
    2023
  • 资助金额:
    $ 101.69万
  • 项目类别:
Colorectal cancer risk factors, risk prediction and blood-based biomarker by tumor consensus molecular subtype
按肿瘤共有分子亚型分类的结直肠癌危险因素、风险预测和血液生物标志物
  • 批准号:
    10591999
  • 财政年份:
    2019
  • 资助金额:
    $ 101.69万
  • 项目类别:
Colorectal cancer risk factors, risk prediction and blood-based biomarker by tumor consensus molecular subtype
按肿瘤共有分子亚型分类的结直肠癌危险因素、风险预测和血液生物标志物
  • 批准号:
    10021547
  • 财政年份:
    2019
  • 资助金额:
    $ 101.69万
  • 项目类别:
Integrated Signaling in Pancreatic Cancer Progression
胰腺癌进展中的整合信号转导
  • 批准号:
    9493432
  • 财政年份:
    2016
  • 资助金额:
    $ 101.69万
  • 项目类别:
Integrated Signaling in Pancreatic Cancer Progression
胰腺癌进展中的整合信号转导
  • 批准号:
    10018467
  • 财政年份:
    2016
  • 资助金额:
    $ 101.69万
  • 项目类别:
Integrated Signaling in Pancreatic Cancer Progression
胰腺癌进展中的整合信号转导
  • 批准号:
    10247023
  • 财政年份:
    2016
  • 资助金额:
    $ 101.69万
  • 项目类别:
Integrated Signaling in Pancreatic Cancer Progression
胰腺癌进展中的整合信号传导
  • 批准号:
    9266771
  • 财政年份:
    2016
  • 资助金额:
    $ 101.69万
  • 项目类别:
Molecular Mediators of Pancreatic Cancer Invasion and Progression
胰腺癌侵袭和进展的分子介质
  • 批准号:
    9250086
  • 财政年份:
    2013
  • 资助金额:
    $ 101.69万
  • 项目类别:
MUCIN GLYCOPROTEINS IN COLON CANCER METASTASIS
结肠癌转移中的粘蛋白糖蛋白
  • 批准号:
    6686311
  • 财政年份:
    2002
  • 资助金额:
    $ 101.69万
  • 项目类别:
Great Lakes New England Clinical Validation Center
新英格兰五大湖临床验证中心
  • 批准号:
    10484455
  • 财政年份:
    2000
  • 资助金额:
    $ 101.69万
  • 项目类别:

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大肠癌发生机制的adenoma-adenocarcinoma pathway同serrated pathway的关系的研究
  • 批准号:
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Synergistic Radiosensitization of Hypoxic Pancreatic Adenocarcinoma using Gd-Texaphyrin Oxygen-Loaded Nanodroplets
使用 Gd-Texaphyrin 载氧纳米液滴对缺氧胰腺腺癌进行协同放射增敏
  • 批准号:
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Expression mechanism of immune checkpoint molecules after carbon-ion radiotherapy in cervical adenocarcinoma specimens
宫颈腺癌碳离子放疗后免疫检查点分子的表达机制
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    23K14913
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Study of fibrosis in pancreatic ductal adenocarcinoma (PDAC) and application of adipose-derived stromal/stem cells for PDAC treatment
胰腺导管腺癌(PDAC)纤维化的研究以及脂肪源性基质/干细胞在 PDAC 治疗中的应用
  • 批准号:
    23K15035
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    2023
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NSD2 在肺腺癌中的治疗靶向
  • 批准号:
    10657069
  • 财政年份:
    2023
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IRAK4 AS A NOVEL IMMUNOTHERAPEUTIC TARGET IN PANCREATIC DUCTAL ADENOCARCINOMA
IRAK4 作为胰腺导管腺癌的新型免疫治疗靶点
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    10442874
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Molecular mechanisms for development of pulmonary invasive mucinous adenocarcinoma
肺浸润性粘液腺癌发生的分子机制
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SGLT2抑制剂治疗糖尿病对肺腺癌的控制机制。
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建立肺小细胞癌腺癌组织学转化模型,探讨小细胞肺癌的治疗策略。
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    23K14614
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Elucidation of the mechanisms of tumor progression controlled by tumor-initiating cells and cancer-associated fibroblasts in pancreatic adenocarcinoma.
阐明胰腺腺癌中肿瘤起始细胞和癌症相关成纤维细胞控制的肿瘤进展机制。
  • 批准号:
    23K15075
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阐明肺腺癌的细胞起源
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