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DESCRIPTION (provided by applicant): Malignant gliomas present great difficulties in treatment, with little change over the past 25 years in the median survival time of 12 months. Current treatment options include surgery, radiotherapy (RT), and chemotherapy. New therapies aimed at suppressing the formation of new vasculature (antiangiogenic treatments), or destroying formed tumor vasculature (vascular disrupting agents) show promise. This application will use magnetic resonance (MR) contrast agents (CAs) and MR detection to measure blood volume, the blood-to-brain transvascular transfer constant, the extravascular extracellular space, and the total extracellular space in cerebral tumors, and also to measure tumor blood flow using MR arterial spin tagging. These parameters present an important summary of the physiology of vasculature, both normal and tumorous. It is proposed to use these vascular parameters as MR biomarkers in animal models of cerebral gliomas. In a series of experiments, we will examine the change in MR-measured vascular parameters after antiangiogenic therapy, after vascular disrupting agent, and after RT, with all MR measures correlated with histopathological assessments of vascular and cellular density in the model tumors. After single-agent therapies are studied, combination therapies will be studied, and MRI vascular biomarkers will be examined as predictors of response as judged both by histopathological assessments and long-term survival. At the completion of these studies, the relation of MR-measured vascular parameters to cellular responses to single and combination therapies will be established, and the utility of MR-measured vascular parameters as predictors of long-term survival assessed. The MR-measured parameters can be translated to clinical use and evaluated as predictors of human tumor response to therapies. These studies represent a first step in a paradigm shift in cancer treatment delivery from a heuristic and formulaic approach to an individualized plan of image guided treatment and response monitoring.
期刊论文(9)
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会议论文
Acute Temporal Changes of MRI-Tracked Tumor Vascular Parameters after Combined Anti-angiogenic and Radiation Treatments in a Rat Glioma Model: Identifying Signatures of Synergism.
在大鼠神经胶质瘤模型中联合抗血管生成和放射治疗后 MRI 跟踪的肿瘤血管参数的急性时间变化:识别协同作用的特征。
DOI: 10.1667/rr14358.1
发表时间: 2017-01
期刊: Radiation research
影响因子: 3.4
作者: [Elmghirbi R, Nagaraja TN, Brown SL, Panda S, Aryal MP, Keenan KA, Bagher-Ebadian H, Cabral G, Ewing JR]
通讯作者: Ewing JR
DOI: 10.1007/s10237-021-01488-8
发表时间: 2021-10
期刊: BIOMECHANICS AND MODELING IN MECHANOBIOLOGY
影响因子: 3.5
作者: [Rey, Julian A., Ewing, James R., Sarntinoranont, Malisa]
通讯作者: Sarntinoranont, Malisa
DOI: 10.1002/mrm.27163
发表时间: 2018-11
期刊: Magnetic resonance in medicine
影响因子: 3.3
作者: [Elmghirbi R, Nagaraja TN, Brown SL, Keenan KA, Panda S, Cabral G, Bagher-Ebadian H, Divine GW, Lee IY, Ewing JR]
通讯作者: Ewing JR
DOI: 10.1371/journal.pone.0084493
发表时间: 2013
期刊: PloS one
影响因子: 3.7
作者: [Nagaraja TN, Aryal MP, Brown SL, Bagher-Ebadian H, Mikkelsen T, Yang JJ, Panda S, Keenan KA, Cabral G, Ewing JR]
通讯作者: Ewing JR
7
    MRI Biomarkers of Response in Cerebral Tumors
    • 批准号:
      8034843
    • 项目类别:
    • 资助金额:
      $30.76万
    • 财政年份:
      2009
    • 负责人:
      JAMES R EWING
    • 依托单位:
    MRI Biomarkers of Response in Cerebral Tumors
    • 批准号:
      8210883
    • 项目类别:
    • 资助金额:
      $30.73万
    • 财政年份:
      2009
    • 负责人:
      JAMES R EWING
    • 依托单位:
    MRI Biomarkers of Response in Cerebral Tumors
    • 批准号:
      7650491
    • 项目类别:
    • 资助金额:
      $31.05万
    • 财政年份:
      2009
    • 负责人:
      JAMES R EWING
    • 依托单位:
    Prediction of Stroke Outcome from Early MRI Data using an Adaptive Neural Network
    • 批准号:
      7626823
    • 项目类别:
    • 资助金额:
      $7.25万
    • 财政年份:
      2008
    • 负责人:
      JAMES R EWING
    • 依托单位:
    海外基金