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临床试验/NCT01235845
NCT01235845Unknown1 期

A Phase I/II Clinical Trial Evaluating DC Activated Cytokine-induced Killer Cell(DCIK) Combined With DC Treatment for Glioma

Qingdao University1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2011年1月1日最近更新:
适应症

试验速览

阶段
1 期
发起方
入组人数
30
试验地点
1
主要终点
To assess the survival of malignant glioma

研究概览

简要总结

Malignant gliomas are very aggressive and among the most common of brain tumors. A diagnosis carries with it a median survival of approximately 12 months, with 90 - 95% of patients surviving less than 2 years. The current standard treatment of surgical resection followed by radiation therapy and chemotherapy has not substantially prolonged survival.

Dendritic cells (DCs) are immune cells that form part of the mammalian immune system. Their main function is to process antigen material and present it on the surface to other cells of the immune system, thus functioning as antigen-presenting cells.In the present study, DCs were used for antigen presentation of glioma antigens to directly induce a cytotoxic T-cell response. Cytokine-induced killer (CIK)cells are shown to be a heterogeneous population, and the major population expresses both the T cell marker CD3 and the NK cell marker CD56, and is termed NKT cells, which has shown significant anti-tumor activity in both clinical trials and animal studies.

Furthermore, CIK cells are able to expand significantly when they are cultured with DCs, and the CIK cells activated by DCs stimulation (DCIKs)have a characteristic which cytotoxic activity enhanced and show increased anti-tumor activity.

This study aimed to evaluate the clinical efficacy of DCIK cells treatment combined with DCs following tumor resection and radiotherapy in patients with malignant glioma.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Female or male, adult patients of 18 to 70 years of age at time of diagnosis that qualify for standard treatment including surgery and radiotherapy.
  • Histologically confirmed diagnosis of 1 of the following malignant gliomas:
  • Anaplastic astrocytoma Glioblastoma multiforme Oligodendroglioma Oligoastrocytoma
  • Newly diagnosed or recurrent disease
  • Patients must have had surgical resection at UCLA for the collection of their tumor. Total, subtotal, or partial resection of more then 70% of tumor mass defined by MRI.
  • After surgery, a pathological diagnosis of malignant glioma (WHO Grade III or IV) will need to be established.
  • Supratentorial tumour localisation.
  • Karnofsky performance status 60-100%
  • Life expectancy ≥ 12 weeks
  • Written informed consent of patient and/or legal guardian.
  • Must be off of steroid at least two weeks prior to vaccination
  • Hematologic and metabolic panel results will be within the parameters of the protocol.
  • Negative pregnancy test
  • Fertile patients must use effective contraception
  • Hepatitis B negative
  • Hepatitis C negative
  • HIV negative
  • Syphilis serology negative
  • Patient must have no prior sensitivity to the components of the dendritic cell vaccine.

排除标准

  • Anti-neoplastic chemotherapy or radiotherapy during 4 weeks before entering the study,
  • Presence of acute infection
  • Inability to obtain informed consent because of psychiatric or complicating medical problems.
  • Unstable or severe intercurrent medical or psychiatric conditions as determined by the Investigator.
  • Subjects with organ allografts.
  • Contraindication to MRI
  • Known history of autoimmune disorder
  • Subjects who have an uncontrolled systemic malignancy that is not in remission.
  • Pregnancy or breast-feeding.
  • Positive for hepatitis B, C, HIV, syphilis
  • Patients unwilling to perform a save method of birth control.

结局指标

主要结局

To assess the survival of malignant glioma

时间窗: 1 year

次要结局

  • To assess the immune response of patients, to assess progression free survival and to evaluate quality of life.(1 year)

研究者

发起方
Qingdao University
申办方类型
Other

研究点 (1)

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