Phase 2 Study of Poly-ICLC in the Treatment of Pediatric Low Grade Gliomas

Poly-ICLC 治疗儿童低级别胶质瘤的 2 期研究

基本信息

  • 批准号:
    9326010
  • 负责人:
  • 金额:
    $ 40万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2014
  • 资助国家:
    美国
  • 起止时间:
    2014-09-05 至 2018-07-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): Brain tumors are the most common solid tumor diagnosed in childhood and thus account for significant childhood mortality in the United States. Low-grade astrocytomas and gliomas (LGG) are the most common type of brain tumor of childhood (36% of childhood brain tumors). Based on data from the Surveillance, Epidemiology, and End Results (SEER) database published in 2009, it is estimated that the incidence of LGG in the pediatric population is 4,600 cases diagnosed annually in the US. Radiotherapy is avoided or delayed in the treatment of LGG to prevent neurocognitive decline and to prevent transformation to a more malignant grade of tumor (grade III and IV). In this proposal, it is hypothesized that LGG are more likely to respond to poly-ICLC (a TLR3 agonist) and that characterization of signaling pathways for TLR3 in the tumor and stromal compartment will predict response to this therapy. This is an open label, multi-institutional, phase 2 clinical trial of poly-ICLC with dosing of 20 mcg/kg body weight/dose administered intramuscularly (IM) twice weekly to determine the radiographic response rate to poly-ICLC in the treatment of children with recurrent or progressive LGG. Total length of therapy will be two years with each cycle being 28 days in length. The three specific aims are to: 1) determine if poly-ICLC has antitumor activity in the treatment of pediatric recurrent LGG, 2) determine the toxicity of this agent in a LGG cohort and to evaluate a QOL endpoint in patients treated with poly-ICLC, and 3) perform extensive molecular profiling of peripheral blood mononuclear cells (PBMCs), serum and cerebral spinal fluid in patients samples before and after treatment with poly-ICLC in an effort to identify a biomarker signature that will predict responsiveness to this therapy.
描述(由申请人提供):

项目成果

期刊论文数量(1)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

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{{ truncateString('DONALD DURDEN', 18)}}的其他基金

Dual PI3K/BRD4 Inhibitory Chemotype for Maximum Inhibition of MYC and Cancer
双重 PI3K/BRD4 抑制化学型可最大程度地抑制 MYC 和癌症
  • 批准号:
    9828553
  • 财政年份:
    2017
  • 资助金额:
    $ 40万
  • 项目类别:
Role of PTEN and PI-3 kinase in medulloblastomagenesis
PTEN 和 PI-3 激酶在髓母细胞瘤发生中的作用
  • 批准号:
    9312006
  • 财政年份:
    2017
  • 资助金额:
    $ 40万
  • 项目类别:
Role of PTEN and PI-3 Kinase in Medulloblastomagenesis
PTEN 和 PI-3 激酶在髓母细胞瘤发生中的作用
  • 批准号:
    10681197
  • 财政年份:
    2017
  • 资助金额:
    $ 40万
  • 项目类别:
Dual PI3K/BRD4 Inhibitory Chemotype for Maximum Inhibition of MYC and Cancer
双重 PI3K/BRD4 抑制化学型可最大程度地抑制 MYC 和癌症
  • 批准号:
    10833761
  • 财政年份:
    2017
  • 资助金额:
    $ 40万
  • 项目类别:
Role of PTEN and PI-3 Kinase in Medulloblastomagenesis
PTEN 和 PI-3 激酶在髓母细胞瘤发生中的作用
  • 批准号:
    10231271
  • 财政年份:
    2017
  • 资助金额:
    $ 40万
  • 项目类别:
Role of PTEN and PI-3 Kinase in Medulloblastomagenesis
PTEN 和 PI-3 激酶在髓母细胞瘤发生中的作用
  • 批准号:
    10196616
  • 财政年份:
    2017
  • 资助金额:
    $ 40万
  • 项目类别:
Dual PI3K/BRD4 Inhibitory Chemotype for Maximum Inhibition of MYC and Cancer
双重 PI3K/BRD4 抑制化学型可最大程度地抑制 MYC 和癌症
  • 批准号:
    10165036
  • 财政年份:
    2017
  • 资助金额:
    $ 40万
  • 项目类别:
Maximizing cancer synthetic lethality using dual PI-3K/PARP inhibitors
使用双重 PI-3K/PARP 抑制剂最大限度地提高癌症合成致死率
  • 批准号:
    9255563
  • 财政年份:
    2016
  • 资助金额:
    $ 40万
  • 项目类别:
A Phase I study of a dual PI3K/BRD4 inhibitor, SF1126 in the treatment of hepatocellular carcinoma | IDE: 74,551
PI3K/BRD4 双重抑制剂 SF1126 治疗肝细胞癌的 I 期研究 |
  • 批准号:
    9167160
  • 财政年份:
    2016
  • 资助金额:
    $ 40万
  • 项目类别:
Maximal MYC control using dual PI-3K/BRD4 (kinase/epigenetic) inhibitors
使用双 PI-3K/BRD4(激酶/表观遗传)抑制剂最大程度地控制 MYC
  • 批准号:
    8834750
  • 财政年份:
    2015
  • 资助金额:
    $ 40万
  • 项目类别:

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