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临床试验/NCT00842790
NCT00842790已完成不适用

Medical and Economical Impact of Predicting the Response to Anti-angiogenic Treatment in Metastatic Renal Cell Carcinoma Using Functional CT and MRI

Assistance Publique - Hôpitaux de Paris1 个研究点 分布在 1 个国家目标入组 107 人开始时间: 2008年9月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
107
试验地点
1
主要终点
RECIST criteria evolution

研究概览

简要总结

The goal is to study the impact of functional MRI and CT evaluation of changes in tumor vessels induced by anti-angiogenic treatment in patients with metastatic RCC.

The hypothesis is that good responders and poor responders will have different responses induced by anti-angiogenic treatment, and that the detection of theses changes by functional imaging can improve the therapeutic management.

Functional CT and MRI will be performed in 200 patients before the beginning of antiangiogenic treatment, 7 days after and every 6 week until tumor progression (as defined by the RECIST criteria). Perfusion and diffusion parameters will be measured using a dedicated software.

详细描述

The aim is to evaluate the capacity of functional CT and functional MRI to measure reliable biomarkers capable of evaluating the efficacy of anti-angiogenic treatment.

Patient and methods

  • Patients 200 patients with metastatic RCC will be enrolled in the study. Patients will be recruited by an oncologist and the images will be acquired by a radiologist.

Patients will be followed until tumor progression (as defined by RECIST) or during 2 years following inclusion if there is no progression.

  • Imaging data acquisition Morphological and functional imaging will be obtained before the beginning of the anti-angiogenic treatment, at 7±2 days and every 6 weeks until tumor progression.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • with metastatic RCC
  • without previous recent antiangiogenic treatment

排除标准

  • severe renal insufficiency
  • allergy to contrast agents
  • pregnancy

结局指标

主要结局

RECIST criteria evolution

时间窗: at day 7 and after every 6 at 16 weeks during 2 years

time-to-progression with anti-angiogenic traitment evaluated by RECIST criteria

次要结局

  • Validation of the technical and acquisition measurement models(at day 7 and after every 6 at 16 weeks during 2 years)
  • Assessment of potential drug costs(at the end)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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