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临床试验/NCT00891904
NCT00891904终止不适用

A Feasibility Study of Re-irradiation Using Stereotactic Body Radiation Therapy (SBRT) and Cetuximab for Recurrent Squamous Cell Carcinoma of the Head and Neck (SCCHN)

Roswell Park Cancer Institute2 个研究点 分布在 1 个国家目标入组 2 人开始时间: 2009年4月最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
2
试验地点
2
主要终点
Grade 4-5 Toxicity as Assessed by NCI CTCAE v.30

研究概览

简要总结

RATIONALE: Stereotactic body radiation therapy may be able to send x-rays directly to the tumor and cause less damage to normal tissue. Monoclonal antibodies, such as cetuximab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Giving stereotactic body radiation therapy together with cetuximab may kill more tumor cells.

PURPOSE: This clinical trial is studying the side effects of radiation therapy given together with cetuximab and to see how well it works in treating patients with recurrent head and neck cancer.

详细描述

OBJECTIVES:

Primary

  • To assess the toxicity of stereotactic body radiotherapy delivered concurrently with cetuximab in patients with recurrent squamous cell carcinoma of the head and neck.

Secondary

  • To assess the feasibility of delivering this regimen in these patients.
  • To assess the impact of this regimen on local control, distant control, and overall survival of these patients.

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 120 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

Grade 4-5 Toxicity as Assessed by NCI CTCAE v.30

时间窗: Daily while on Treatment

次要结局

  • Feasibility as Assessed According to Ability to Deliver the Entire Treatment Regimen to 80% of Patients(2 years)
  • Local and Distant Control(very 2 months for year one, every 3-4 months for year 2, every 6 months for years 3 and 4 and annually thereafter.)
  • Overall Survival(very 2 months for year one, every 3-4 months for year 2, every 6 months for years 3 and 4 and annually thereafter)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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