Cone-beam CT Guided Stereotactic Radiation Therapy for Locally Advanced Pancreatic Cancer
研究概览
详细说明
Objective of the study:
To determine safety and technical feasibility of stereotactic radiotherapy for locally advanced pancreatic carcinoma
Study design:
Pilot study to determine safety and feasibility
Study population:
Patients with locally advanced pancreatic carcinoma, without distant metastasis
Intervention:
Patients will undergo endoscopic fiducial marker placement, and patients will get a custom-made individual corset. Radiotherapy will be delivered in three fractions of 8 Gy on an outpatient basis.
Primary study outcome:
The main study endpoint will be safety of the procedure, expressed in proportion of patients experiencing treatment-induced toxicity grade 3 or more according to the CTC-AE 4.0 due to the complete procedure within 90 days of the last radiation.
Secondary study outcome:
Other study parameters will be technical feasibility, treatment response, quality of life, overall survival, progression free survival, and rate of possible secondary resections
Nature and extent of the burden and risks associated with participation, benefit and group relatedness:
Increased severe toxicity may occur due to the intervention, but treatment related toxicity should be limited due to strict dose constraints to the organs at risk (e.g. duodenum, stomach). Potential benefits may be pain relief, due to local control of the tumor, and a prolonged survival.
研究类型
注册 (预期的)
阶段
- 阶段2
联系人和位置
学习地点
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-
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Utrecht、荷兰、3584 CX
- 招聘中
- University Medical Center Utrecht
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接触:
- M. van Vulpen, Prof MD PhD
- 电话号码:+31 88 755 8800
- 邮箱:m.vanvulpen@umcutrecht.nl
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首席研究员:
- M. van Vulpen, Prof MD PhD
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Locally advanced pancreatic tumors (stage III) or medically inoperable patients with pancreatic cancer (stage I, II, or III)
- Not eligible for operation with curative intent
- >18 years
- Written informed consent
Exclusion Criteria:
- WHO performance status 3-4
- Expected life span <3 months
- Previous chemotherapy, pancreatic surgery or pancreatic radiotherapy
- Exclusion criteria for contrast enhanced MRI and/or CT scan, following the protocol of the department of radiology UMCU
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:irradiation
24 Gy in 3 fractions
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Safety
大体时间:90 days of last irradiation
|
Safety of the procedure, expressed in proportion of patients experiencing treatment-induced toxicity grade 3 or more according to the CTC-AE 4.0 due to the complete procedure within 90 days of the last radiation
|
90 days of last irradiation
|
合作者和调查者
赞助
调查人员
- 首席研究员:M. van Vulpen, Prof MD PhD、UMC Utrecht
出版物和有用的链接
研究记录日期
研究主要日期
学习开始
初级完成 (预期的)
研究完成 (预期的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.