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TNF Blockade in Pancreatic Cancer Patients

TNF Blockade in Pancreatic Cancer Patients
胰腺癌患者中的 TNF 阻断
批准号:
6733908
负责人:
MIGUEL A VILLALONA-CALERO
金额:
$33.26万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-09-30 至 2005-08-31

项目摘要

项目成果

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中文摘要
翻译
描述(由申请人提供):晚期胰腺癌患者预后不良,中位生存期不到12个月,表明明显需要更有效的治疗。此外,胰腺癌患者经常因恶病质、厌食、恶心/呕吐和腹痛而虚弱。促炎性细胞因子如肿瘤坏死因子(TNF)α、白细胞介素6(IL-6)和白细胞介素1(IL-1)都已被发现在胰腺癌患者中升高,并且除了直接促进肿瘤进展的可能性之外,还与引起许多这些症状有关。抗癌治疗的一个潜在靶点是阻断TNF的作用。我们推测TNF阻断剂可以使化疗更耐受,改善生活质量,延缓肿瘤进展。在目前的建议中,我们寻求在转移性或复发性胰腺癌患者中进行的先导性试验中,将联合收割机标准化疗(吉西他滨)和TNF阻断与可溶性TNF受体分子(依那西普)相结合。我们将评估TNF阻断是否可以改善临床获益反应、生活质量和化疗后6个月的癌症无进展生存率。此外,将从外周血单核细胞裂解物中获得TNF和其他炎性细胞因子以及转录因子NF-κ B(TNF刺激肿瘤生长的候选途径)的系列水平。还将在接受吉西他滨作为单一药剂的10名患者的对照组中测量生活质量以及细胞因子和NF-κ B的水平。在接受TNF阻断的患者中观察到的生活质量或无进展生存期的益处将鼓励在适当把握度的随机临床试验中评估这种新策略。
英文摘要
DESCRIPTION (provided by applicant): The poor prognosis of patients with advanced pancreatic adenocarcinoma, with a median survival of less than 12 months, indicates an obvious need for more effective treatments. In addition, patients with pancreatic carcinoma are frequently debilitated by cachexia, anorexia, nausea/vomiting and abdominal pain. Pro-inflammatory cytokines like tumor necrosis factor (TNF) alpha, interleukin 6 (IL-6) and interleukin 1 (IL-1) have all been found to be elevated in pancreatic cancer patients and have been implicated in causing many of these symptoms, in addition to the possibility of directly promoting tumor progression. One potential target for anticancer therapy is blocking the effects of TNF. We hypothesize that TNF blockade should make chemotherapy more tolerable, should improve quality of life and should retard the time to tumor progression. In the current proposal, we seek to combine standard chemotherapy (gemcitabine) and TNF blockade with soluble TNF receptor molecules (etanercept) in a pilot trial in patients with metastatic or recurrent pancreatic cancer. We will evaluate if TNF blockade can improve the clinical benefit response, quality of life and the rate of cancer progression-free survival at six months obtained with chemotherapy. In addition, serial levels of TNF and other inflammatory cytokines, as well as the transcription factor NF-kappaB, a candidate pathway through which TNF stimulates tumor growth, will be obtained from peripheral blood mononuclear cells lysates. Quality of life and levels of the cytokines and NF-kappaB will also be measured in a control group of 10 patients receiving gemcitabine as a single agent. The observation of benefits in either quality of life or progression-free survival in patients undergoing TNF blockade would encourage evaluation of this novel strategy in properly powered randomized clinical trials.
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Targeting Somatic Homologous Recombination in Solid Tumors
  • 批准号:
    8101174
  • 项目类别:
  • 资助金额:
    $52.22万
  • 财政年份:
    2010
  • 负责人:
    MIGUEL A VILLALONA-CALERO
  • 依托单位:
Targeting Somatic Homologous Recombination in Solid Tumors
  • 批准号:
    8204586
  • 项目类别:
  • 资助金额:
    $51.66万
  • 财政年份:
    2010
  • 负责人:
    MIGUEL A VILLALONA-CALERO
  • 依托单位:
海外基金