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临床试验/NCT01336985
NCT01336985终止1 期

Phase Ib Study of the Safety and Pharmacokinetics of Chemoembolization With Irinotecan-Eluting Beads for the Treatment of Hepatic Metastases

National Institutes of Health Clinical Center (CC)2 个研究点 分布在 1 个国家目标入组 5 人开始时间: 2011年3月28日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
终止
入组人数
5
试验地点
2
主要终点
To determine the safety of hepatic chemoembolization with drug-eluting beads containing 100mg of irinotecan

研究概览

简要总结

Background:

  • Cancers in other parts of the body often spread to the liver, developing tumors which in many instances cannot be removed with surgery. Liver chemoembolization is a treatment that is routinely performed to control liver tumors in those who cannot have surgery. It has been shown to prolong survival, but does not cure the cancer. During chemoembolization very tiny beads (drug-eluting beads, or DEB) containing chemotherapy drugs (usually doxorubicin) are administered directly into the blood vessels of a liver tumor. The drug within the beads is then released into the tumor whilethe beads temporarily interrupt the tumor s blood supply.
  • Irinotecan, a drug commonly given intravenously to treat colon cancer, has been given in chemoembolization procedures in four other studies that have shown that the treatment is generally well tolerated. Researchers are interested in determining whether giving the drug irinotecan directly into the liver using drug-eluting beads is not only well tolerated but also provides a larger dose directly to the tumor as determined by tumor and normal liver tissue biopsies. The liver biopsies are an optional portion of the study.

Objectives:

  • To evaluate the safety and effectiveness of chemoembolization with irinotecan for tumors caused by cancer that has spread to the liver.

Eligibility:

  • Individuals at least 18 years of age who have melanoma, colon, or another intra-abdominal cancer that has spread to the liver.

Design:

  • Participants will be screened with a physical examination, medical history, blood tests, tumor imaging studies, and liver biopsies.
  • Participants will receive up to 3 DEB chemoembolization treatments about 6 weeks apart.
  • After two treatments, participants will have imaging studies to see if the tumors have shrunk, and those whose tumors have shrunk may have a third treatment.
  • Multiple liver biopsies may be performed and blood samples will be taken to determine how much drug is in the tumor and the circulation, and to see how the tumor reacts to the drug.
  • Participants will return for followup visits for up to 1 year....

详细描述

Background:

  • Clinical evidence suggests that hepatic chemoembolization may prolong survival in patients with hepatic metastases.
  • Early studies have indicated that chemoembolization using irinotecan drug eluting beads may be more effective in treating hepatic metastases from colon or melanoma primary tumors.

Objectives:

  • Primary Objective:

--To determine the safety of hepatic chemoembolization with drug-eluting beads containing 100mg of irinotecan

  • Secondary Objectives:

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 84 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

To determine the safety of hepatic chemoembolization with drug-eluting beads containing 100mg of irinotecan

次要结局

  • To determine the serum pharmacokinetics and tumor tissue concentrations achieved following hepatic chemoembolization with irinotecan-eluting beads

研究者

研究点 (2)

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