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临床试验/NCT00155766
NCT00155766Unknown1 期

A Pilot Study for the Immunotherapy of Recurrent Cervical Cancers Using Dendritic Cells (DCs) Pulsed With Human Papillomavirus Type 16 E7 Antigen

National Taiwan University Hospital1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2003年1月1日最近更新:
适应症

试验速览

阶段
1 期
入组人数
12
试验地点
1
主要终点
1. Safety issues in patients receiving HPV16 E7 peptide-pulsed autologous DCs immunotherapy

研究概览

简要总结

Chemotherapy is the current standard treatment for unresectable recurrent cervical carcinoma after radiotherapy or distant metastasis of cervical carcinoma. The most effective regimens are cisplatin-based chemotherapy. After failure of the cisplatin-based chemotherapy, there is still no treatment that has been proved to be effective.

Human papilloma viruses (HPV) have been consistently implicated in causing cervical cancer especially those high-risk types (HPV 16,18,31,45) have been strongly associated with cervical cancer. HPV 16 was found in more than 50% of cervical cancer tissues. Results from many animal tumor models have indicated that immunization with tumor antigen-pulsed dendritic cells can trigger a long-lasting anti-tumor immune response and significantly inhibit the growth of implanted tumor cells. Recently, many clinical trials have been conducted to evaluate the feasibility and safety of immunizing cancer patients with tumor antigen-pulsed dendritic cells. No severe toxicity has been reported and some patients were shown to respond to the treatment. Based on previous animal and clinical studies by other investigators, we propose to evaluate the potential of immunizing cancer patients with antigen-pulsed autologous dendritic cells as a cancer vaccine to treat for recurrent cervical cancers after failure of cisplatin-based chemotherapy treatment or refusing chemotherapy. In this study, we will generate dendritic cells by culturing patient's autologous PBMC with GM-CSF and IL-4 in vitro. These dendritic cells will be pulsed with synthetic peptides representing the CTL epitopes on HPV Type 16 E7. Antigen-pulsed dendritic cells will be injected into inguinal lymph nodes under the guidance of real-time sonography. Each patient will receive four injections and 12 patients in total will be recruited for this study.

详细描述

Chemotherapy is the current standard treatment for unresectable recurrent cervical carcinoma after radiotherapy or distant metastasis of cervical carcinoma. The most effective regimens are cisplatin-based chemotherapy. After failure of the cisplatin-based chemotherapy, there is still no treatment that has been proved to be effective.

Human papilloma viruses (HPV) have been consistently implicated in causing cervical cancer especially those high-risk types (HPV 16,18,31,45) have been strongly associated with cervical cancer. HPV 16 was found in more than 50% of cervical cancer tissues. Results from many animal tumor models have indicated that immunization with tumor antigen-pulsed dendritic cells can trigger a long-lasting anti-tumor immune response and significantly inhibit the growth of implanted tumor cells. Recently, many clinical trials have been conducted to evaluate the feasibility and safety of immunizing cancer patients with tumor antigen-pulsed dendritic cells. No severe toxicity has been reported and some patients were shown to respond to the treatment. Based on previous animal and clinical studies by other investigators, we propose to evaluate the potential of immunizing cancer patients with antigen-pulsed autologous dendritic cells as a cancer vaccine to treat for recurrent cervical cancers after failure of cisplatin-based chemotherapy treatment or refusing chemotherapy. In this study, we will generate dendritic cells by culturing patient's autologous PBMC with GM-CSF and IL-4 in vitro. These dendritic cells will be pulsed with synthetic peptides representing the CTL epitopes on HPV Type 16 E7. Antigen-pulsed dendritic cells will be injected into inguinal lymph nodes under the guidance of real-time sonography. Each patient will receive four injections and 12 patients in total will be recruited for this study.

研究设计

研究类型
Interventional
分配方式
Non Randomized
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 75 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • recurrent cervical cancer
  • HPV 16 infection
  • Previously received cisplatin ot 5-FU based chemotherapy or refused to receive chemotherapy
  • HLA-A2 haplotype
  • Older than 20 years old
  • ECOG I or II
  • Life expectancy longer than 3 months
  • Adequate bone marrow reserve
  • pregnancy test: negative
  • Informed consent obtained

排除标准

  • CNS metastasis
  • Acute or chronic infection
  • Pregnant or lactating women
  • Cardiac diseases such as heart failure, unstable angina, arrhythmia, myocardial infarction
  • Autoimmune disease
  • Previously other cancers (except basal cell cancer)
  • Without chemotherapy, biotherapy for more than 6 weeks

结局指标

主要结局

1. Safety issues in patients receiving HPV16 E7 peptide-pulsed autologous DCs immunotherapy

次要结局

  • 1. Immunologic responses in patients receiving HPV16 E7 peptide-pulsed autologous DCs immunotherapy
  • 2. Clinical response in patients receiving HPV16 E7 peptide-pulsed autologous DCs immunotherapy

研究者

申办方类型
Other

研究点 (1)

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